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# Dia.Pro

Diagnostic Bioprobes s.r.l

## Sitemaps

- [XML Sitemap](https://www.diapro.it/sitemap.xml): Contains all public & indexable URLs for this website.

## Posts

- [CLIA & ELISA AUTOMATION](https://www.diapro.it/clia-elisa-automation/) - COVID-19 IgM Monitoring of the immune response to COVID-19, in the early stage of the infection as an additional marker to PCR
- [VECTOR-BORNE DISEASES INCREASING](https://www.diapro.it/vector-borne-diseases-increased-cases-outbreaks/) - COVID-19 IgM Monitoring of the immune response to COVID-19, in the early stage of the infection as an additional marker to PCR
- [EXPORT CHAMPIONS 2023](https://www.diapro.it/export-champions-2023/) - COVID-19 IgM Monitoring of the immune response to COVID-19, in the early stage of the infection as an additional marker to PCR

## Events

- [AMCLI](https://www.diapro.it/zkevent/amcli/) - Integrated Technologies for clinical microbiology & molecular diagnostics
- [WHL Labs/Medlab Africa/Africa Health](https://www.diapro.it/zkevent/medlab-africa/) - The leading laboratory exhibition in the African region will be back on 2-4 September 2025
- [WHX Labs Kuala Lumpur](https://www.diapro.it/zkevent/medlab-asia/) - WHX Labs Kuala Lumpur
- [Clinical Lab Expo](https://www.diapro.it/zkevent/aacc/) - The Clinical Lab Expo is the world's premier gathering for laboratory medicine, with laboratory scientists from a broad range of specialties expected to attend.
- [MEDICA](https://www.diapro.it/zkevent/medica/) - Dive into the future – live in Düsseldorf and digital. Here the whole world of medicine meets. A must for anyone wanting to experience tomorrow’s healthcare market live.
- [ISBT](https://www.diapro.it/zkevent/isbt/) - Join us for the 35th Regional Congress of the ISBT from June 1 – 4, 2025 in Milan, Italy! Organized by the International Society of Blood Transfusion (ISBT), in conjunction with the Società Italiana di Medicina Trasfusionale e Immunoematologia, the Regional Congress in Milan will bring together transfusion medicine specialists from around the globe, to
- [ESCMID Global](https://www.diapro.it/zkevent/eccmid/) - Congress of the European Society of Clinical Microbiology and Infectious Diseases
- [WHX Labs Dubai](https://www.diapro.it/zkevent/whx-labs-dubai/) - With a remarkable increase in both attendees and exhibitor registrations, WHX Labs Dubai formerly Medlab Middle East is gearing up for its return 3-6 February 2025 at the Dubai World Trade Centre. This 24th edition promises to be a landmark event, spotlighting cutting-edge advancements and sustainable practices in laboratory medicine. Over 800+ exhibitors from 40+ countries,

## Panels

- [Blood Screening - CLIA](https://www.diapro.it/panels/blood-screening-clia/) - Assays are intended to be used only in combination with the fully automated Random Access platform S.A.R.A.
- [MISCELLANY - PCR](https://www.diapro.it/panels/serology-pcr/)
- [Trasplantation - PCR](https://www.diapro.it/panels/trasplantation-pcr/)
- [Hepatitis - PCR](https://www.diapro.it/panels/hepatitis-pcr/)
- [COVID-19 - PCR](https://www.diapro.it/panels/covid-19-pcr/)
- [Serology - ELISA](https://www.diapro.it/panels/serology-elisa/)
- [COVID-19 - ELISA](https://www.diapro.it/panels/covid-19-elisa/)
- [Blood Screening - ELISA](https://www.diapro.it/panels/blood-screening-elisa/)
- [Autoimmunity - ELISA](https://www.diapro.it/panels/autoimmunity-elisa/)
- [Hepatitis - ELISA](https://www.diapro.it/panels/hepatitis-elisa/)
- [Tropical Diseases - ELISA](https://www.diapro.it/panels/tropical-diseases-elisa/)
- [TORCH - ELISA](https://www.diapro.it/panels/torch-elisa/)
- [Serology - CLIA](https://www.diapro.it/panels/serology-clia/) - Assays are intended to be used in combination only with the fully automated Random Access platform S.A.R.A.
- [Tropical Diseases - CLIA](https://www.diapro.it/panels/tropical-diseases-clia/) - Assays are intended to be used in combination only with the fully automated Random Access platform S.A.R.A..
- [TORCH - CLIA](https://www.diapro.it/panels/torch-clia/) - Assays are intended to be used in combination only with the fully automated Random Access platform S.A.R.A.
- [Autoimmunity - CLIA](https://www.diapro.it/panels/autoimmunity-clia/) - Assays are intended to be used in combination only with the fully automated Random Access platform S.A.R.A.
- [COVID-19 - CLIA](https://www.diapro.it/panels/covid-19-clia/) - Assays are intended to be used in combination only with the fully automated Random Access platform S.A.R.A.

## Products

- [Syphilis Ab One Version ULTRA - ELISA](https://www.diapro.it/products/syphilis-ab-one-version-ultra-elisa-2/) - Enzyme ImmunoAssay (ELISA) for the one-step FAST qualitative determination of antibodies (IgG, IgM and IgA) to Treponema Pallidum in human plasma and sera. The kit is intended for the screening of blood units and the follow-up of Tp-infected patients. For “in vitro” diagnostic use only. Microplates are coated with purified Treponema pallidum synthetic antigens (p15,
- [CHLAMYDIA TRACHOMATIS DNA - PCR](https://www.diapro.it/products/chlamydia-trachomatis-dna-pcr/) - The Chlamydia trachomatis DNA Real-Time PCR kit coded CTDNA.CE is intended for the qualitative detection of Chlamydia trachomatis DNA in human urethral/cervical swabs and urine with a simultaneous control of the extraction/amplification reaction through an Internal Control (IC). The kit has been adapted for the use on the Real-Time Thermacyclers and ABI 7500 Sequence Detection
- [TRYPANOSOMA CRUZI DNA - PCR](https://www.diapro.it/products/trypanosoma-cruzi-dna-pcr/) - The Trypanosoma cruzi DNA Real-Time PCR kit coded TCRUZIDNA.CE is intended for the qualitative detection of Trypanosoma cruzi DNA in human blood samples with a simultaneous control of the extraction/amplification reaction through an Internal Control (IC). The kit has been adapted for the use on the Real-Time Thermacyclers and ABI 7500 Sequence Detection System® (Software
- [Toxoplasma Gondii DNA - PCR](https://www.diapro.it/products/toxoplasma-gondii-dna-pcr/) - The Toxoplasma gondii DNA Real-Time PCR kit coded TOXODNA.CEis intended for the qualitative detection of Toxoplasma Gondii DNA in human samples (plasma and amniotic fluid) with a simultaneous control of the extraction/amplification reaction through an Internal Control (IC).
- [LEGIONELLA PNEUMOPHILA DNA - PCR](https://www.diapro.it/products/legionella-pneumophila-dna-pcr/) - Legionella pneumophila, a gram negative non spore forming motile bacillus, is the etiologicagent of Legionellosis. Clinical symphtoms can range in severity from a mild, febrile illness(Pontiac fever) to a rapid and potentially fatal pneumonia (Legionnaires’ disease). L. pneumophila is a common cause of nosocomial and travel-acquired pneumonia and with thebacterial species Mycoplasma pneumoniae and Clamydia
- [Parvovirus B19 IgM - ELISA](https://www.diapro.it/products/parvovirus-b19-igm-elisa/) - Enzyme ImmunoAssay (ELISA) for the qualitative determination of IgM antibodies to Parvovirus B19 in human plasma and sera. For “in vitro” diagnostic use only. The B19 virus, generally referred to as parvovirus B19 was the first (and until 2005 the only) known human virus in the family of parvoviruses, genus erythrovirus. Parvovirus B19 is a
- [Parvovirus B19 IgG - ELISA](https://www.diapro.it/products/parvovirus-b19-igg-elisa/) - Enzyme ImmunoAssay (ELISA) for the quantitative/qualitative determination of IgG antibodies to Parvovirus B19 in human plasma and sera. For “in vitro” diagnostic use only. The B19 virus, generally referred to as parvovirus B19 was the first (and until 2005 the only) known human virus in the family of parvoviruses, genuserythrovirus. Parvovirus B19 is a non-enveloped,
- [DIA.CHEMILUX Malaria Ab](https://www.diapro.it/products/dia-chemilux-malaria-ab/) - Chemi-Luminescence ImmunoAssay (CLIA) for the semi-quantitative determination of total antibodies (IgG&A&M) to Plasmodium species (Malaria) in human plasma and sera. The kit is intended for the screening of anti Malaria antibodies in blood units and the follow-up of infected patients. The devise does not type antibodies into IgG&A&M but detects the totality of them. The
- [Toxo IgM - ELISA](https://www.diapro.it/products/toxo-igm-elisa/) - Enzyme ImmunoAssay (ELISA) for the determination of IgM antibodies to Toxoplasma gondii or T.gondii in human plasma and sera with the “capture” system. The devise is intended for the follow-up of T.gondii infected patients and for the monitoring of risk of neonatal defects due to T.gondii infection during pregnancy. For “in vitro” diagnostic use only.
- [Toxo IgG - ELISA](https://www.diapro.it/products/toxo-igg-elisa/) - Enzyme ImmunoAssay (ELISA) for the quantitative/qualitative determination of IgG antibodies to Toxoplasma gondii in plasma and sera.The solid phase is first treated with the diluted sample and IgG to T. gondii are captured, if present, by the antigens. After washing out all the other components of the sample, in the 2nd incubation bound anti Toxoplasma
- [TETOX IgG - ELISA](https://www.diapro.it/products/tetox-igg-elisa/) - Enzyme ImmunoAssay (ELISA) for the quantitative determination of IgG antibodies to Tetanus toxoid in human serum and plasma. Tetanus is caused by an infection with the bacterium Clostridium tetani which is commonly found in soil, dust and manure. Tetanus occurs in all parts of the world but is most frequent in hot and wet climates
- [Syphilis IgM - ELISA](https://www.diapro.it/products/syphilis-igm-elisa/) - Enzyme ImmunoAssay (ELISA) for the determination of IgM antibodies to Treponema pallidum (Tp) in human plasma and sera. The kit is intended for the follow-up of Tp-infected patients. For “in vitro” diagnostic use only. Microplates are coated with Tp immunodominant synthetic antigens (recombinant p47, p17 and TmpA).In the 1st incubation, the solid phase is treated
- [RUB IgM - ELISA](https://www.diapro.it/products/rub-igm-elisa/) - Enzyme ImmunoAssay (ELISA) for the determination of IgM antibodies to Rubella Virus in human plasma and sera with the “capture” system. The devise is intended for the follow-up of Rubella Virus infected patients and for the monitoring of risk of neonatal defects due to Rubella Virus infection during pregnancy. For “in vitro” diagnostic use only.
- [RUB IgG - ELISA](https://www.diapro.it/products/rub-igg-elisa/) - Enzyme ImmunoAssay (ELISA) for the quantitative/qualitative determination of IgG antibodies to Rubella Virus in human plasma and sera. For “in vitro” diagnostic use only. Microplates are coated with native Rubella Virus, highly purified by sucrose gradient centrifugation and inactivated. The solid phase is first treated with the diluted sample and IgG to Rubella Virus are
- [Meningitis IgG - ELISA](https://www.diapro.it/products/meningitis-igg-elisa/) - Enzyme ImmunoAssay (ELISA) for the determination of IgG antibodies to groups ACWY Meningococcus in human plasma and sera. The product is intended for the follow-up of patients administered with a meningococcal vaccine, containing the polysaccharides from groups A, C, Y and W135. Micro-plates are coated with a preparation of purified capsular polysaccharides formed by serogroups
- [Measles virus IgM - ELISA](https://www.diapro.it/products/measles-virus-igm-elisa/) - Enzyme ImmunoAssay (ELISA) for the qualitative determination of IgM antibodies to Measles Virus in human plasma and sera. The product is intended mostly for the identification of the pathogen in patients undergoing an exanthematic infection. Micro-plates are coated with Measles Virus native antigens derived from tissue culture of a virulent strain. In the 1st incubation,
- [Measles virus IgG - ELISA](https://www.diapro.it/products/measles-virus-igg-elisa/) - Enzyme ImmunoAssay (ELISA) for the semi-quantitative determination of IgG antibodies to Measles Virus in human plasma and sera. The product is intended mostly for the follow-up of anti Measles Virus vaccination and can also be useful for the follow up of infected individuals. Micro-plates are coated with Measles Virus native antigens derived from tissue culture
- [HSV 2 IgM - ELISA](https://www.diapro.it/products/hsv-2-igm-elisa/) - Enzyme ImmunoAssay (ELISA) for the determination of IgM antibodies to Herpes Simplex Virus types 2 in human plasma and sera with the “capture” system. The devise is intended for the follow-up of HSV2 infected patients and for the monitoring of risk of neonatal defects due to HSV infection during pregnancy. For “in vitro” diagnostic use
- [HSV 2 IgG - ELISA](https://www.diapro.it/products/hsv-2-igg-elisa/) - Enzyme ImmunoAssay (ELISA) for the quantitative/qualitative determination of IgG antibodies to Herpes Simplex Virus type 2 in human plasma and sera. For “in vitro” diagnostic use only. Microplates are coated with synthetic HSV2 specific glycoprotein G or gG. The solid phase is first treated with the diluted sample and IgG to HSV2 are captured, if
- [HSV 1&2 IgM - ELISA](https://www.diapro.it/products/hsv-12-igm-elisa/) - Enzyme ImmunoAssay (ELISA) for the determination of IgM antibodies to Herpes Simplex Virus types 1&2 in human plasma and sera with the “capture” system. The devise is intended for the follow-up of HSV infected patients and for the monitoring of risk of neonatal defects due to HSV infection during pregnancy. For “in vitro” diagnostic use
- [HSV 1&2 IgG - ELISA](https://www.diapro.it/products/hsv-12-igg-elisa/) - Enzyme ImmunoAssay (ELISA) for the quantitative/qualitative determination of IgG antibodies to Herpes Simplex Virus type 1 and 2 in human plasma and sera. For “in vitro” diagnostic use only. Microplates are coated with native inactivated HSV1 and HSV2. The solid phase is first treated with the diluted sample and IgG to HSV are captured, if
- [HSV 1 IgM - ELISA](https://www.diapro.it/products/hsv-1-igm-elisa/) - Enzyme ImmunoAssay (ELISA) for the determination of IgM antibodies to Herpes Simplex Virus types 1 in human plasma and sera with the “capture” system. The device is intended for the follow-up of HSV1 infected patients and for the monitoring of risk of neonatal defects due to HSV infection during pregnancy.For “in vitro” diagnostic use only.
- [HSV 1 IgG - ELISA](https://www.diapro.it/products/hsv-1-igg-elisa/) - Enzyme ImmunoAssay (ELISA) for the quantitative/qualitative determination of IgG antibodies to Herpes Simplex Virus type 1 in human plasma and sera. For “in vitro” diagnostic use only. Microplates are coated with native inactivated HSV1. The solid phase is first treated with the diluted sample and IgG to HSV are captured, if present, by the antigens.
- [HP IgM - ELISA](https://www.diapro.it/products/hp-igm-elisa/) - Enzyme ImmunoAssay (ELISA) for the determination of IgM antibodies to Helicobacter pylori in human plasma and sera. For “in vitro” diagnostic use only. Microplates are coated with H.pylori immunodominant antigens derived from tissue culture of a virulent strain. In the 1st incubation, the solid phase is treated with diluted samples and anti-HP IgM are captured,
- [HP IgG - ELISA](https://www.diapro.it/products/hp-igg-elisa/) - Enzyme ImmunoAssay (ELISA) for the quantitative/qualitative determination of IgG antibodies to Helicobacter pylori in human plasma and sera. The product is intended for the follow-up of patients showing gastrointestinal pathologies potentially correlated to HP infection. For “in vitro” diagnostic use only. Microplates are coated with H.pylori immunodominant antigens derived from tissue culture of a virulent
- [HP IgA - ELISA](https://www.diapro.it/products/hp-iga-elisa/) - Enzyme ImmunoAssay (ELISA) for the quantitative/qualitative determination of IgA antibodies to Helicobacter pylori in human plasma and sera. The product is intended for the follow-up of patients showing gastrointestinal pathologies referable to H.pylori infection.For “in vitro” diagnostic use only. Microplates are coated with H.pylori immunodominant antigens derived from tissue culture of a virulent strain. In
- [HP CagA IgG - ELISA](https://www.diapro.it/products/hp-caga-igg-elisa/) - Enzyme Immunoassay for the quantitative determination of IgG antibodies to Helicobacter pylori cytotoxin associated gene A Antigen or CagA-Ag in sera/plasma. The product is intended for the follow-up of patients showing gastrointestinal pathologies referable to H.pylori infection. For “in vitro” diagnostic use only. Microplates are coated with Helicobacter pylori specific CagA-Ag synthetic antigen. In the
- [HP CagA IgA - ELISA](https://www.diapro.it/products/hp-caga-iga-elisa/) - Enzyme Immunoassay for the quantitative determination of IgA antibodies to Helicobacter pylori cytotoxin associated gene A Antigen or CagA-Ag in sera/plasma. The product is intended for the follow-up of patients showing gastrointestinal pathologies referable to H.pylori infection. For “in vitro” diagnostic use only. Microplates are coated with Helicobacter pylori specific CagA-Ag synthetic antigen. In the
- [HP Ag - ELISA](https://www.diapro.it/products/hp-ag-elisa/) - Enzyme Immunoassay for the qualitative/quantitative determination of Helicobacter pylori Antigen in human stools The kit may be used for the follow-up of HP-infected patients and their pharmacological treatment. For “in vitro” diagnostic use only. Stools from patients are used as a source of sample for the determination of HP antigen. Microplates are coated with a
- [Extraction Kit for H.Pylori Ag - ELISA](https://www.diapro.it/products/extraction-kit-for-h-pylori-ag-elisa/) - H.Pylori Ag antigen STOOL EXTRACTION KIT
- [EBV VCA IgM - ELISA](https://www.diapro.it/products/ebv-vca-igm-elisa/) - Enzyme ImmunoAssay (ELISA) for the quantitative or qualitative determination of IgM class antibodies to Epstein Barr Virus (EBV) Capsidic Antigen in human plasma and sera with the “capture” system. The kit is intended for the classification of the viral infective agent and the follow-up of EBV infected patients. For “in vitro” diagnostic use only. Epstein
- [EBV VCA IgG - ELISA](https://www.diapro.it/products/ebv-vca-igg-elisa/) - Enzyme ImmunoAssay (ELISA) for the quantitative/qualitative determination of IgG antibodies to Epstein Barr Virus Capsidic Antigen in human plasma and sera. For “in vitro” diagnostic use only. Epstein Barr Virus or EBV is the principal etiological agent of infectious mononucleosis, as well as a contributory factor in the etiology of Burkitt’s lymphoma and nasopharyngeal carcinoma,
- [EBV VCA IgA - ELISA](https://www.diapro.it/products/ebv-vca-iga-elisa/) - Enzyme ImmunoAssay (ELISA) for the quantitative/qualitative determination of IgA antibodies to Epstein Barr Virus Capsidic Antigen in human plasma and sera. For “in vitro” diagnostic use only. Epstein Barr Virus or EBV is the principal etiological agent of infectious mononucleosis, as well as a contributory factor in the etiology of Burkitt’s lymphoma and nasopharyngeal carcinoma,
- [EBV EBNA IgM - ELISA](https://www.diapro.it/products/ebv-ebna-igm-elisa/) - Enzyme ImmunoAssay (ELISA) for the qualitative determination of IgM class antibodies to Epstein Barr Virus Nuclear Antigen (EBNA) in human plasma and sera.The kit is intended for the classification of the viral infective agent and the follow-up of EBV infected patients.For “in vitro” diagnostic use only.Epstein Barr Virus or EBV is the principal etiological agent
- [EBV EBNA IgG - ELISA](https://www.diapro.it/products/ebv-ebna-igg-elisa/) - Enzyme ImmunoAssay (ELISA) for the quantitative/qualitative determination of IgG antibodies to Epstein Barr Virus Nuclear Antigen in human plasma and sera. For “in vitro” diagnostic use only.Epstein Barr Virus or EBV is the principal etiological agent of infectious mononucleosis, as well as a contributory factor in the etiology of Burkitt’s lymphoma and nasopharyngeal carcinoma, or
- [Ea IgM - ELISA](https://www.diapro.it/products/ea-igm-elisa/) - Enzyme ImmunoAssay (ELISA) for the qualitative determination of IgM class antibodies to Epstein Barr Virus Early Antigen (Ea) in human plasma and sera. The kit is intended for the classification of the viral infective agent and the follow-up of EBV infected patients. For “in vitro” diagnostic use only.Epstein Barr Virus or EBV is the principal
- [Ea IgG - ELISA](https://www.diapro.it/products/ea-igg-elisa/) - Enzyme ImmunoAssay (ELISA) for the quantitative/qualitative determination of IgG antibodies to Epstein Barr Virus Early Antigen in human plasma and sera. For “in vitro” diagnostic use only. Epstein Barr Virus or EBV is the principal etiological agent of infectious mononucleosis, as well as a contributory factor in the etiology of Burkitt’s lymphoma and nasopharyngeal carcinoma,
- [CoxB IgM - ELISA](https://www.diapro.it/products/coxb-igm-elisa/) - Enzyme Immuno Assay (ELISA) for the determination of IgM antibodies to Coxsackievirus type B (CoxB) in human plasma and sera. For “in vitro” diagnostic use only. Coxsackievirus belongs to a group of viruses called enteroviruses in particular they are Picornaviruses.They are present in two main groups, A and B. Most Coxsackievirus infections are not serious.
- [CoxB IgG - ELISA](https://www.diapro.it/products/coxb-igg-elisa/) - Enzyme Immuno Assay (ELISA) for the determination of IgG antibodies to Coxsackievirus type B (CoxB) in human plasma and sera. For “in vitro” diagnostic use only. Coxsackievirus belongs to a group of viruses called enteroviruses in particular they are Picornaviruses.They are present in two main groups, A and B. Most Coxsackievirus infections are not serious.
- [Chlamydia Trachomatis IgM - ELISA](https://www.diapro.it/products/chlamydia-trachomatis-igm-elisa/) - Enzyme ImmunoAssay (ELISA) for the determination of IgM antibodies to Chlamydia Trachomatisin human plasma and sera. For “in vitro” diagnostic use only. The determination of species-specific IgG, IgM and IgA is a helpful tool for the clinician to identify the infective agent and to decide the right therapy. The kit is intended for the follow
- [Chlamydia Trachomatis IgG - ELISA](https://www.diapro.it/products/chlamydia-trachomatis-igg-elisa/) - Enzyme ImmunoAssay (ELISA) for the quantitative determination of IgG antibodies specific to Chlamydia trachomatis in human plasma and sera. The kit is intended for the follow up of patients undergoing a Chlamydia trachomatis infection. For in vitro diagnostic use only. Microplates are coated with an immunodominant species-specific polypeptide derived from Chlamydia trachomatis major outer-membrane antigen
- [Chlamydia Trachomatis IgA - ELISA](https://www.diapro.it/products/chlamydia-trachomatis-iga-elisa/) - Enzyme ImmunoAssay (ELISA) for the qualitative determination of IgA antibodies to Chlamydia Trachomatis in human plasma and sera. The product is intended for the follow-up of patients showing pathologies referable to Chl. Trachomatis infection. For “in vitro” diagnostic use only. Microplates are coated with a species-specific polypeptide derived from C.trachomatis major outer membrane antigen. In
- [Chlamydia Pneumoniae IgM - ELISA](https://www.diapro.it/products/chlamydia-pneumoniae-igm-elisa/) - Enzyme ImmunoAssay (ELISA) for the determination of IgM antibodies to Chlamydia Pneumoniae in human plasma and sera. The product is intended for the follow-up of patients showing respiratory pathologies referable to Chl. pneumoniae infection. Micro-plates are coated with a preparation of native C.pneumoniae. In the 1st incubation, the solid phase is treated with diluted samples
- [Chlamydia Pneumoniae IgG - ELISA](https://www.diapro.it/products/chlamydia-pneumoniae-igg-elisa/) - Enzyme ImmunoAssay (ELISA) for the quantitative determination of IgG antibodies to Chlamydia pneumoniae in human plasma and sera. The kit is intended for the follow up of patients undergoing a Chlamydia pneumoniae infection. Micro-plates are coated with a preparation of native C.pneumoniae. In the 1st incubation, the solid phase is treated with diluted samples and
- [Chlamydia Pneumoniae IgA - ELISA](https://www.diapro.it/products/chlamydia-pneumoniae-iga-elisa/) - Enzyme ImmunoAssay (ELISA) for the qualitative determination of IgA antibodies to Chlamydia Pneumoniae in human plasma and sera. The product is intended for the follow-up of patients showing respiratory pathologies referable to Chl. Pneumoniae infection. Micro-plates are coated with a preparation of native C.pneumoniae. In the 1st incubation, the solid phase is treated with diluted
- [CMV IgM - ELISA](https://www.diapro.it/products/cmv-igm-elisa/) - Enzyme Immuno Assay (ELISA) for the determination of IgM class antibodies to Cytomegalovirus or CMV in human plasma and sera with the “capture” system. The kit is intended for the follow-up of CMV infected patients and the monitoring of the risk of neonatal defects due to CMV infection during pregnancy. For “in vitro” diagnostic use
- [HBc IgM - ELISA](https://www.diapro.it/products/hbc-igm-elisa/) - Enzyme ImmunoAssay (ELISA) for both the quantitative and qualitative determination of antibodies to the Surface Antigen of Hepatitis B Virus in human plasma and sera. For “in vitro” diagnostic use only. After washing, captured antibodies are detected by an HBsAg, labelled with peroxidase (HRP), that specifically binds the second available binding site of these antibodies.
- [HBs Ag Confirmation - ELISA](https://www.diapro.it/products/hbs-ag-confirmation-elisa/) - In the screening of blood units for Hepatitis B surface Antigen or HBsAg some false positivity may happen, leading to a misinterpretation of the assay results and a misclassification of the blood unit and the donor. To confirm the positivity of a screened sample or to confirm the presence of an ongoing HBV infection in
- [HBs Ab - ELISA](https://www.diapro.it/products/hbs-ab-elisa/) - Enzyme ImmunoAssay (ELISA) for both the quantitative and qualitative determination of antibodies to the Surface Antigen of Hepatitis B Virus in human plasma and sera. For “in vitro” diagnostic use only. After washing, captured antibodies are detected by an HBsAg, labelled with peroxidase (HRP), that specifically binds the second available binding site of these antibodies.
- [HBe Ag&Ab - ELISA](https://www.diapro.it/products/hbe-agab-elisa/) - Enzyme ImmunoAssay (ELISA) for the determination of Hepatitis B Virus “e” Antigen and Antibody in human plasma and sera. The kit is intended for the follow-up of acute infection and of chronic patients under therapy. For “in vitro” diagnostic use only. HBeAg, if present in the sample, is captured by a specific monoclonal antibody, in
- [HCV Ab Confirmation - ELISA](https://www.diapro.it/products/hcv-ab-confirmation-elisa/) - Hepatitis C Virus or HCV is an enveloped RNA virus recently classified in the family of Flaviviridae. The genome encodes for structural components, a nucleocapsid protein and two envelope glycoproteins, and functional constituents involved in the virus replication and protein processing. The nucleocapsid-encoding region seems to be the most conservative among the isolates obtained all
- [HDV Ab - ELISA](https://www.diapro.it/products/hdv-ab-elisa/) - Competitive Enzyme ImmunoAssay (ELISA) for the determination of antibodies to Hepatitis Delta Virus or HDV in human plasma and sera with a “two-steps” methodology. The kit is used for the follow-up of patients infected by HDV. For “in vitro” diagnostic use only. Anti-HDV antibodies, if present in the sample, compete with a virus-specific polyclonal IgG,
- [HDV Ag - ELISA](https://www.diapro.it/products/hdv-ag-elisa/) - Third generation Enzyme ImmunoAssay (ELISA) for the determination of Hepatitis Delta Virus or HDV in human plasma and sera. The kit is intended for the follow-up of HDV infected patients. For “in vitro” diagnostic use only. HDV Ag, if present in the sample, is captured by a specific monoclonal antibody, in the 1st incubation. A
- [HDV IgM - ELISA](https://www.diapro.it/products/hdv-igm-elisa/) - Enzyme ImmunoAssay (ELISA) for the determination of IgM class antibodies to Hepatitis Delta Virus or HDV in human plasma and sera with the “capture” system. The kit is intended for the classification of the viral infective agent and the follow-up of HDV infected patients. For “in vitro” diagnostic use only. Microplates are coated with a
- [HEV IgM - ELISA](https://www.diapro.it/products/hev-igm-elisa/) - Enzyme ImmunoAssay (ELISA) for the determination of IgM antibodies to Hepatitis E Virus in human plasma and sera. The kit may be used for the determination of the acute phase of infection where IgM antibodies are generated before the other immunoglobulins and for the follow-up of HEV-infected patients. For “in vitro” diagnostic use only. Microplates
- [HEV IgG - ELISA](https://www.diapro.it/products/hev-igg-elisa/) - Third generation Enzyme ImmunoAssay (ELISA) for the qualitative determination of IgG antibodies to Hepatitis E Virus in human plasma and sera. The kit is intended for the follow-up of HEV-infected patients. For “in vitro” diagnostic use only. Microplates are coated with HEV-specific recombinant antigens encoding for conservative and immunodominant determinants of all the 4 subtypes.
- [HEV Ab (Version ULTRA) - ELISA](https://www.diapro.it/products/hev-ab-version-ultra-elisa/) - Third generation Enzyme ImmunoAssay (ELISA) for the qualitative determination of total antibodies to Hepatitis E Virus (HEV) in serum and plasma. The kit is intended for the follow-up of HEV-infected patients and the screening of blood units. In addition, due to the assay configuration of the product, the kit may be used also in testing
- [HAV IgM - ELISA](https://www.diapro.it/products/hav-igm-elisa/) - Enzyme ImmunoAssay (ELISA) for the determination of IgM class antibodies to Hepatitis A Virus in human plasma and sera with the “capture” system. The kit may be used for the identification of the viral agent causing hepatitis in the patient and the follow up of the acute phase of the infection. For “in vitro” diagnostic
- [HAV Ab - ELISA](https://www.diapro.it/products/hav-ab-elisa/) - Competitive Enzyme ImmunoAssay (ELISA) for the determination of antibodies to Hepatitis A Virus in human plasma and sera. The kit is used for the follow-up of patients infected by HAV. For “in vitro” diagnostic use only. The assay is based on the principle of competition where the antibodies in the sample compete with an anti-HAV
- [HTLV I&II Ab (Version ULTRA) - ELISA](https://www.diapro.it/products/htlv-iii-ab-version-ultra-elisa/) - Enzyme ImmunoAssay (ELISA) for the qualitative determination of antibodies to Human T-cell Lymphotropic Virus type I&II or HTLV I&II Ab. The kit is for use in screening of blood units and the follow-up of HTLV I&II-infected patients. For “in vitro” diagnostic use only. HTLV I&II are retroviruses not related genetically to HIV1&2; however, they have similar
- [HIV Ab&Ag - ELISA](https://www.diapro.it/products/hiv-abag-elisa/) - Fourth generation Enzyme Immunoassay for the determination of antibodies to Human Immunodeficiency Virus or HIV type 1&2&O and P24 HIV-1 Antigen in human serum and plasma. This kit is intended exclusively for In vitro diagnostic use in an authorized clinical laboratory and the test has to be carried out by specifically trained health-care professional personnel.
- [Syphilis Ab (Version ULTRA) - ELISA](https://www.diapro.it/products/syphilis-ab-version-ultra-elisa/) - Enzyme ImmunoAssay (ELISA) for the determination of antibodies to Treponema pallidum (Tp) in human plasma and sera. The kit is for use in screening of blood units and the follow-up of Tp-infected patients. For “in vitro” diagnostic use only. Microplates are coated with purified Treponema pallidum synthetic antigens, derived from immunodominant protein of the bacterium. The
- [HBs Ag (Version ULTRA) - ELISA](https://www.diapro.it/products/hbs-ag-version-ultra-elisa/) - Fourth generation Enzyme Immunoassay (ELISA) for the one-step determination of Hepatitis B surface Antigen or HBsAg in human plasma and sera & for the screening of blood units. Able to detect HBsAg mutants and find application in the follow-up of HBV-infected patients. For “in vitro” diagnostic use only. The World Health Organization (WHO) defines Hepatitis B Virus
- [HBc Ab - ELISA](https://www.diapro.it/products/hbc-ab-elisa/) - Competitive Enzyme ImmunoAssay (ELISA) for the determination of antibodies to Hepatitis B core Antigen in human plasma and sera. The kit is for use in screening of blood units and the follow-up of HBV-infected patients. For “in vitro” diagnostic use only. The assay is based on the principle of competition where the antibodies in the sample
- [HCV Ab - ELISA](https://www.diapro.it/products/hcv-ab-elisa/) - Fourth generation Enzyme ImmunoAssay (ELISA) for the determination of antibodies to Hepatitis C Virus in human plasma/sera & for the screening of blood units and follow-up of HCV-infected patients. For “in vitro” diagnostic use only. Microplates are coated with HCV-specific antigens derived from “core” and “ns” regions encoding for conservative and immunodominant antigenic determinants (Core peptide, recombinant
- [Malaria Ab - ELISA](https://www.diapro.it/products/malaria-ab-elisa/) - 3rd Generation Enzyme Immunoassay for the determination of antibodies to Plasmodium species in human serum and plasma. The kit is intended for the screening of blood units and the identification of people that came into contact with the protozoa and developed an immunological response. The kit is for in vitro diagnostic use only and the
- [T.cruzi Ab - ELISA](https://www.diapro.it/products/t-cruzi-ab-elisa/) - Third generation Enzyme Immuno Assay (ELISA) for the determination of antibodies to Tripanosoma cruzi (Tc) in human plasma and sera. The kit may be used for the screening of blood units and the follow-up of Tc-infected patients. For “in vitro” diagnostic use only. Tripanosomes are flagellar protozoa known to infect humans and cause the Chaga’s
- [ZIKA Virus IgG - ELISA](https://www.diapro.it/products/zika-virus-igg-elisa/) - INTRODUCTION The Zika virus belongs to Flaviviridae and the genus Flavivirus, and is thus related to the dengue, yellow fever, Japanese encephalitis, and West Nile viruses. Like other flaviviruses, Zika virus is enveloped and icosahedral and has a nonsegmented, single-stranded, positive-sense RNA genome. The RNA genome genes encode for nonstructural proteins and structural proteins, whose
- [ZIKA Virus IgM - ELISA](https://www.diapro.it/products/zika-virus-igm-elisa/) - INTRODUCTION The Zika virus belongs to Flaviviridae and the genus Flavivirus, and is thus related to the dengue, yellow fever, Japanese encephalitis, and West Nile viruses. Like other flaviviruses, Zika virus is enveloped and icosahedral and has a nonsegmented, single-stranded, positive-sense RNA genome. The RNA genome genes encode for nonstructural proteins and structural proteins, whose
- [Dengue virus NS1 Antigen - ELISA](https://www.diapro.it/products/dengue-virus-ns1-antigen-elisa/) - Qualitative or semi-quantitative Enzyme Immunoassay (ELISA) for the determination of Dengue virus NS1 Antigen in human plasma and sera. The kit is intended for the identification of Dengue Virus (DNGV) infected patients, in particular in the first acute infection when antibodies are not present.
- [Dengue virus IgM - ELISA](https://www.diapro.it/products/dengue-virus-igm-elisa/) - Enzyme ImmunoAssay (ELISA) for the qualitative determination of IgM antibodies to Dengue Virus in human plasma and sera. Micro-plates are coated with higly purified Dengue Virus antigen.In the 1st incubation, the solid phase is treated with diluted samples and anti Dengue Virus IgM are captured, if present, by the antigens.After washing out all the other
- [Dengue virus IgG - ELISA](https://www.diapro.it/products/dengue-virus-igg-elisa/) - Enzyme ImmunoAssay (ELISA) for the qualitative/semiquantitative determination of IgG antibodies to Dengue virus in human plasma and sera. The product is intended mostly for the follow-up of Dengue virus infection.The product is supplied for research purpose only.Micro-plates are coated with an highly purified Dengue virus antigen. In the 1st incubation, the solid phase is treated
- [West Nile Virus IgM antibodies - ELISA](https://www.diapro.it/products/west-nile-virus-igm-antibodies-elisa/) - Enzyme ImmunoAssay (ELISA) for the qualitative determination of IgM antibodies to West Nile Virus (WNV) in human plasma and sera collected from patients suspected of an ongoing West Nile Virus infection or at risk of it. For “in vitro” diagnostic use only. Diagnosis of WNV is generally obtained through detection of virus-specific IgG and IgM
- [West Nile Virus IgG antibodies - ELISA](https://www.diapro.it/products/west-nile-virus-igg-antibodies-elisa/) - Enzyme ImmunoAssay (ELISA) for the qualitative and semi quantitative determination of IgG antibodies to West Nile Virus (WNV) in human plasma and sera. Diagnosis of WNV is generally obtained through detection of virus-specific IgG and IgM antibodies IgM against the most immunodominant antigens of the virus (ENV and NS1) by means of ELISA techniques. While
- [West Nile Virus Antibodies - ELISA](https://www.diapro.it/products/west-nile-virus-antibodies-elisa/) - Enzyme ImmunoAssay (ELISA) for the qualitative determination of antibodies to West Nile Virus in human plasma and sera. The product is intended mostly for the follow-up of West Nile Virus infection. For “in vitro” diagnostic use only. West Nile Virus is an arbovirus and is transmitted to people through complex life cycles involving birds and
- [Yellow Fever Virus IgG - ELISA](https://www.diapro.it/products/yellow-fever-virus-igg-elisa/) - Enzyme ImmunoAssay (ELISA) for the determination of IgG antibodies to Yellow Fever Virus (YFV) in human plasma and sera coming from naturally infected people and vaccinated subjects to monitor the presence of protective IgG. Yellow Fever virus is an RNA Flavivirus of the family of Flaviviridae transmitted by the mosquito “Aedes Aegypti”, causing a severe
- [CMV IgG - ELISA](https://www.diapro.it/products/cmv-igg-elisa/) - Enzyme ImmunoAssay (ELISA) for the quantitative/qualitative determination of IgG antibodies to Cytomegalovirus in plasma and sera. For “in vitro” diagnostic use only. Microplates are coated with native Cytomegalovirus antigens, highly purified by sucrose gradient centrifugation and inactivated. The solid phase is first treated with the diluted sample and IgG to Cytomegalovirus are captured, if present,
- [IgG anti U1 - sn RNP68 - ELISA](https://www.diapro.it/products/igg-anti-u1-sn-rnp68-elisa/) - Enzyme ImmunoAssay (ELISA) for the quantitative determination of IgG autoantibodies to RNP-68KDa in human plasma and sera. For in vitro diagnostic use only. Microplates are coated with a preparation of recombinant U1-snRNP 68 antigen. In the 1st incubation, the solid phase is treated with diluted samples and anti U1-snRNP 68 IgG are captured, if present,
- [IgG anti SSB - ELISA](https://www.diapro.it/products/igg-anti-ssb-elisa/) - The device SSB.CE is an Enzyme ImmunoAssay (ELISA) intended to be used for the quantitative determination of IgG autoantibodies against SSB autoantigens in human plasma and sera. For in vitro diagnostic use only. Microplates are coated with a preparation of recombinant SSB antigen. In the 1st incubation, the solid phase is treated with diluted samples
- [IgG anti SSA 52 KD - ELISA](https://www.diapro.it/products/igg-anti-ssa-52-kd-elisa/) - The device SSA52.CE is an Enzyme ImmunoAssay (ELISA) intended to be used for the quantitative determination of IgG autoantibodies against SSA-52KD autoantigens in human plasma and sera. For in vitro diagnostic use only. Microplates are coated with a preparation of Recombinant SSA 52KDa antigen. In the 1st incubation, the solid phase is treated with diluted
- [IgG anti Sm - ELISA](https://www.diapro.it/products/igg-anti-sm-elisa/) - The device SM.CE is an Enzyme ImmunoAssay (ELISA) intended to be used for the quantitative determination of IgG autoantibodies against Sm autoantigens in human plasma and sera. For in vitro diagnostic use only. Microplates are coated with a preparation of purified Sm antigen. In the 1st incubation, the solid phase is treated with diluted samples
- [IgG anti Centromere B - ELISA](https://www.diapro.it/products/igg-anti-centromere-b-elisa/) - The device CENPB.CE is an Enzyme ImmunoAssay (ELISA) intended to be used for the quantitative determination of IgG autoantibodies against Centromere B autoantigens in human plasma and sera. For in vitro diagnostic use only. Microplates are coated with a preparation of recombinant Centromere B antigen. In the 1st incubation, the solid phase is treated with
- [IgG anti SSA 60 KD - ELISA](https://www.diapro.it/products/igg-anti-ssa-60-kd-elisa/) - The device SSA60.CE is an Enzyme ImmunoAssay (ELISA) intended to be used for the quantitative determination of IgG autoantibodies against SSA-60KD autoantigens in human plasma and sera. For in vitro diagnostic use only. Microplates are coated with a preparation of recombinant SSA 60KDa antigen. In the 1st incubation, the solid phase is treated with diluted
- [IgG anti Scl-70 - ELISA](https://www.diapro.it/products/igg-anti-scl-70-elisa/) - The device SCL70.CE is an Enzyme ImmunoAssay (ELISA) intended to be used for the quantitative determination of IgG autoantibodies against Scl-70 autoantigens in human plasma and sera. For in vitro diagnostic use only. Microplates are coated with a preparation of recombinant Scl-70 antigen. In the 1st incubation, the solid phase is treated with diluted samples
- [IgG anti Jo-1 - ELISA](https://www.diapro.it/products/igg-anti-jo-1-elisa/) - The device JO1.CE is an Enzyme ImmunoAssay (ELISA) intended to be used for the quantitative determination of IgG autoantibodies against Jo-1 autoantigens in human plasma and sera. For in vitro diagnostic use only. Microplates are coated with a preparation of recombinant Jo-1 antigen. In the 1st incubation, the solid phase is treated with diluted samples
- [ENA 6 parameters profile - ELISA](https://www.diapro.it/products/ena-6-parameters-profile-elisa/) - The device ENA6PRO.CE is an Enzyme ImmunoAssay (ELISA) intended to be used for the qualitative determination of IgG autoantibodies against Ro/SSA, La/SSB, RNP-68, Sm, Scl-70, Jo-1 in human plasma and sera. For in vitro diagnostic use only.
- [ANA Screening IgG - ELISA](https://www.diapro.it/products/ana-screening-igg-elisa/) - Enzyme ImmunoAssay (ELISA) for the qualitative determination of IgG auto-antibodies to dsDNA, histones, SSA, SSB, Sm, Sm/RNP, Scl-70, Jo-1, centromere and other antigens extracted from the HEp-2 nucleus, in human plasma and sera. For in vitro diagnostic use only.
- [ANA 8 parameters profile - ELISA](https://www.diapro.it/products/ana-8-parameters-profile-elisa/) - Enzyme ImmunoAssay (ELISA) for the qualitative determination of IgG auto-antibodies to Ro/SSA 60KDa, Ro/SSA 52KDa, La/SSB, RNP-68, Sm, Scl-70, Jo-1, CENPB, in human plasma and sera. For in vitro diagnostic use only.
- [ENA Screening IgG - ELISA](https://www.diapro.it/products/ena-screening-igg-elisa/) - Enzyme ImmunoAssay (ELISA) for the qualitative determination of IgG auto-antibodies to SSA, SSB, Sm, RNP68, Scl-70, Jo-1, in human plasma and sera. For in vitro diagnostic use only. Autoimmunity is the failure of an organism to recognize its own constituent parts as self, which allows an immune response against its own cells and tissues. Any
- [COVID-19 Spike 1&2 IgG - ELISA](https://www.diapro.it/products/covid-19-igg-elisa-2/) - INTENDED USE Enzyme ImmunoAssay (ELISA) for the semi-quantitative determination of IgG antibodies to COVID-19 Spike antigens in human plasma and sera. The IgG assay is intended for testing: (a) health-care workers at risk of COVID-19 infection to verify whether or not they might be positive for potentially neutralizing anti Spike IgG; (b) normal population for
- [COVID-19 IgM - ELISA](https://www.diapro.it/products/covid-19-igm-elisa/) - INTENDED USE Enzyme ImmunoAssay (ELISA) for the determination of IgM antibodies to COVID19 in human plasma and sera. The kit is intended for the monitoring of the immune response to COVID-19 in the early stage of the infection as an additional marker to PCR. For “in vitro” diagnostic use only.
- [COVID-19 IgG Confirmation - ELISA](https://www.diapro.it/products/covid-19-igg-confirmation-elisa/) - INTENDED USE Module-based Enzyme-Immuno-Assay (ELISA) for the confirmation of samples positive for IgG antibodies to covid-19 in first screening. The test can be used in addition to identify the specificity of antibodies to the major immunodominant covid-19 antigens. For “in vitro” diagnostic use only.
- [COVID-19 IgG - ELISA](https://www.diapro.it/products/covid-19-igg-elisa/) - INTENDED USE Enzyme ImmunoAssay (ELISA) for the determination of IgG antibodies to COVID19-specific Nucleocapsid (“Core”) and Spike antigens in human plasma and sera. The kit is intended for monitoring the immune response to COVID-19. The IgG assay is recommended in particular for testing: (a) infected individuals in follow-up serological testing and when recovered from the
- [COVID-19 IgA - ELISA](https://www.diapro.it/products/covid-19-iga-elisa/) - INTENDED USE Enzyme ImmunoAssay (ELISA) for the determination of IgA antibodies to COVID19 in human plasma and sera. The IgA assay is recommended, in addition to IgG and IgM, to: a) monitor the global immunological response of patients undergoing an acute infection and their follow-up to full recovery; b) and specifically for testing patients with
- [COVID-19 IgG/IgM Confirmation and Typing - ELISA](https://www.diapro.it/products/covid-19-igg-igm-confirmation-and-typing-elisa/) - Module-based Enzyme-Immuno-Assay (ELISA) for the confirmation of samples positive for IgG and IgM antibodies to COVID-19 in first screening. The test is particularly useful in monitoring patients, infected by COVID-19, from the time of symptoms offset up to full recovery. The test can be used in addition to identify (a) the specificity (“typing”) of antibodies
- [ACE2-RBD Neutralization Assay - ELISA](https://www.diapro.it/products/ace2-rbd-neutralization-assay-elisa/) - INTENDED USE Enzyme ImmunoAssay (ELISA) for the semi-quantitative determination of inhibition activity of RBD-ACE2 binding induced by antibodies to SARS-CoV-2 in human plasma and sera. The assay is intended for: Confirmation of anti RBD antibodies neutralizing activity in patients positively recovered from covid-19 showing antibodies to Spike/RBD; human donors, recovered from COVID-19 infection, positive for
- [DIA. CHEMILUX HTLV I&II Ab](https://www.diapro.it/products/dia-chemilux-htlv-iii-ab/) - Chemi-Luminescence ImmunoAssay (CLIA) for the determination of antibodies to T-cell Lymphotropic Virus type I&II in human plasma and sera. The kit may be used for the screening of blood units and the follow-up of HTLV I&II-infected patients, not for typing HTLV I&II. The device has been adapted for the use in exclusive combination with the
- [DIA. CHEMILUX HIV Ab&Ag](https://www.diapro.it/products/dia-chemilux-hiv-abag/) - Chemi-Luminescence ImmunoAssay (CLIA) for the diagnostic screening of antibodies to all subtypes of HIV-1 and HIV-2 and HIV-1 antigen (p24) in human serum or plasma and the follow up of HIV- infected patients. This kit is intended exclusively for In vitro diagnostic use in an authorized clinical laboratory and the test has to be carried
- [DIA. CHEMILUX Syphilis Ab](https://www.diapro.it/products/dia-chemilux-syphilis-ab/) - Chemi-Luminescence ImmunoAssay (CLIA) for the qualitative determination of antibodies (IgG, IgM and IgA) to Treponema Pallidum. The kit may be used for the screening of blood units and the follow-up of Tp-infected patients.
- [DIA. CHEMILUX T cruzi Ab](https://www.diapro.it/products/dia-chemilux-t-cruzi-ab/) - Chemi-Luminescence ImmunoAssay (CLIA) for the qualitative determination of antibodies to Trypanosoma cruzi (Tc) in human plasma and sera. The kit is intended for the screening of blood units and the follow-up of Tc-infected patients. The device has been adapted for the use in exclusive combination with the Dia.Pro instrument named SARA.
- [DIA. CHEMILUX HEV Ab](https://www.diapro.it/products/dia-chemilux-hev-ab/) - Chemi-Luminescence ImmunoAssay (CLIA) for the semi-quantitative determination of total antibodies (IgG&A&M) to Hepatitis E Virus (HEV) in human plasma and sera. The kit is intended for the follow-up of HEV infected patients. The devise does not type antibodies into IgG&A&M but detects the totality of them. The device has been adapted for the use in
- [DIA. CHEMILUX HDV Ab](https://www.diapro.it/products/dia-chemilux-hcv-ab-2/) - Chemi-Luminescence ImmunoAssay (CLIA) for the determination of antibodies to Hepatitis D Virus in human plasma and sera. . The device has been adapted for the use in exclusive combination with the Dia.Pro instrument named SARA.
- [DIA.CHEMILUX HBcAb](https://www.diapro.it/products/dia-chemilux-hbcab/) - Chemi-Luminescence ImmunoAssay (CLIA) for the Qualitative/Quantitative determination of Hepatitis CORE surface Antigen Total Antibodies or HBcAb in human plasma and sera. The kit is intended for the screening of blood units and the follow-up of HBV-infected patients. The device has been adapted for the use in exclusive combination with the Dia.Pro instrument named SARA.
- [DIA. CHEMILUX HCV Ab](https://www.diapro.it/products/dia-chemilux-hcv-ab/) - Chemi-Luminescence ImmunoAssay (CLIA) for the determination of antibodies to Hepatitis C Virus in human plasma and sera. The kit may be used for the screening of blood units and the follow-up of HCV-infected patients. The device has been adapted for the use in exclusive combination with the Dia.Pro instrument named SARA.
- [DIA. CHEMILUX HBs Ag](https://www.diapro.it/products/dia-chemilux-hbs-ag/) - Chemi-Luminescence ImmunoAssay (CLIA) for the quantitative determination of Hepatitis B surface Antigen or HBsAg in human plasma and sera. The kit may be used for the screening of blood units, is able to detect HBsAg mutants and find application in the follow-up of HBV-infected patients. The device has been adapted for the use in exclusive
- [DIA.CHEMILUX Dengue Virus Ab - CLIA](https://www.diapro.it/products/dia-chemilux-dengue-virus-ab-clia/) - Chemi-Luminescence ImmunoAssay (CLIA) for the semi-quantitative determination of total antibodies (IgG&A&M) to Dengue Virus (DNGV) in human plasma and sera. The kit is intended for the follow-up of DNGV infected patients and in addition may be used for the screening of blood units. The devise does not type antibodies into IgG&A&M but detects the totality
- [DIA.CHEMILUX CHIKV Ab - CLIA](https://www.diapro.it/products/dia-chemilux-chikv-ab-clia/) - Chemi-Luminescence ImmunoAssay (CLIA) for the semi-quantitative determination of total antibodies (IgG&A&M) to Chikungunya Virus (CHIKV) in human plasma and sera. The kit is intended for the follow-up of CHIKV at-risk or infected patients and in addition might be used for the screening of blood units. The devise does not type antibodies into IgG&A&M but detects
- [DIA.CHEMILUX ZIKV Ab - CLIA](https://www.diapro.it/products/dia-chemilux-zikv-ab-clia/) - Chemi-Luminescence ImmunoAssay (CLIA) for the semi-quantitative determination of total antibodies (IgG&A&M) to ZIKA Virus (ZIKV) in human plasma and sera. The kit is intended for the follow-up of ZIKV infected patients and in addition may be used for the screening of blood units. The devise does not type antibodies into IgG&A&M but detects the totality
- [DIA. CHEMILUX Toxoplasma IgM](https://www.diapro.it/products/dia-chemilux-toxoplasma-igm/) - Immunocapture based ChemiLuminescence ImmunoAssay (CLIA) for the determination of IgM antibodies to Toxoplasma in human plasma and sera. The device has been adapted for the use in exclusive combination with the Dia.Pro instrument named SARA.
- [DIA. CHEMILUX Toxoplasma IgG](https://www.diapro.it/products/dia-chemilux-toxoplasma-igg/) - Chemi-Luminescence ImmunoAssay (CLIA) for the quantitative determination of IgG antibodies to Toxoplasma in human plasma and sera. The device has been adapted for the use in exclusive combination with the Dia.Pro instrument named SARA.
- [DIA. CHEMILUX Rubella IgM](https://www.diapro.it/products/dia-chemilux-rubella-igm/) - Immunocapture based ChemiLuminescence ImmunoAssay (CLIA) for the determination of IgM antibodies to Rubella virus in human plasma and sera from patients undergoing an acute infection and from women in pregnancy monitoring. The device has been adapted for the use in exclusive combination with the Dia.Pro instrument named SARA.
- [DIA. CHEMILUX Rubella IgG](https://www.diapro.it/products/dia-chemilux-rubella-igg/) - Chemi-Luminescence ImmunoAssay (CLIA) for the quantitative determination of IgG antibodies to Rubella Virus in human plasma and sera. The device has been adapted for the use in exclusive combination with the Dia.Pro instrument named SARA.
- [DIA. CHEMILUX HSV2 IgM](https://www.diapro.it/products/dia-chemilux-hsv2-igm/) - Chemi-Luminescence ImmunoAssay (CLIA) for the determination of IgM antibodies to Herpes Simplex Virus type 2 in human plasma and sera. The devise is intended for the follow-up of HSV infected patients and for the monitoring of risk of neonatal defects due to HSV infection during pregnancy. The device has been adapted for the use in
- [DIA. CHEMILUX HSV2 IgG](https://www.diapro.it/products/dia-chemilux-hsv2-igg/) - Chemi-Luminescence ImmunoAssay (CLIA) for the quantitative/qualitative determination of IgG antibodies to Herpes Simplex Virus type 2 in human plasma and sera. The device has been adapted for the use in exclusive combination with the Dia.Pro instrument named SARA.
- [DIA. CHEMILUX HSV1&2 IgM](https://www.diapro.it/products/dia-chemilux-hsv12-igm/) - Chemi-Luminescence ImmunoAssay (CLIA) for the determination of IgM antibodies to Herpes Simplex Virus type 1 and 2 in human plasma and sera. The device is intended for the follow-up of HSV infected patients and for the monitoring of risk of neonatal defects due to HSV infection during pregnancy. The device has been adapted for the
- [DIA. CHEMILUX HSV1&2 IgG](https://www.diapro.it/products/dia-chemilux-hsv12-igg/) - Chemi-Luminescence ImmunoAssay (CLIA) for the quantitative/qualitative determination of IgG antibodies to Herpes Simplex Virus type 1 and 2 in human plasma and sera. The device has been adapted for the use in exclusive combination with the Dia.Pro instrument named SARA.
- [DIA. CHEMILUX HSV1 IgM](https://www.diapro.it/products/dia-chemilux-hsv1-igm/) - Chemi-Luminescence ImmunoAssay (CLIA) for the qualitative determination of IgM antibodies to Herpes Simplex Virus type 1 in human plasma and sera. The devise is intended for the follow-up of HSV infected patients and for the monitoring of risk of neonatal defects due to HSV infection during pregnancy. The device has been adapted for the use
- [DIA. CHEMILUX HSV1 IgG](https://www.diapro.it/products/dia-chemilux-hsv1-igg/) - Chemi-Luminescence ImmunoAssay (CLIA) for the quantitative/qualitative determination of IgG antibodies to Herpes Simplex Virus type 1 in human plasma and sera. The device has been adapted for the use in exclusive combination with the Dia.Pro instrument named SARA.
- [DIA. CHEMILUX Cytomegalovirus IgM](https://www.diapro.it/products/dia-chemilux-cytomegalovirus-igm/) - Immunocapture based Chemi-Luminescence Immuno-Assay (CLIA) for the determination of IgM antibodies specific to Cytomegalovirus in human plasma and sera from patients undergoing an acute CMV infection, virus reactivation and from women in pregnancy monitoring. The device has been adapted for the use in exclusive combination with the Dia.Pro’s instrument named SARA.
- [DIA. CHEMILUX Cytomegalovirus IgG](https://www.diapro.it/products/dia-chemilux-cytomegalovirus-igg/) - Chemi-Luminescence ImmunoAssay (CLIA) for the quantitative determination of IgG antibodies to Cytomegalovirus in human plasma and sera. The device has been adapted for the use in exclusive combination with the Dia.Pro instrument named SARA.
- [DIA. CHEMILUX TOXOID IgG](https://www.diapro.it/products/dia-chemilux-toxoid-igg/) - Chemi-Luminescence ImmunoAssay (CLIA) for the quantitative determination of IgG antibodies to Tetanus Toxoid in human plasma and sera. The device has been adapted for the use in exclusive combination with the Dia.Pro instrument named SARA.
- [HDV RNA Retrotrascription kit - PCR](https://www.diapro.it/products/hdv-rna-pcr/) - The HDV RNA Retrotrascription kit coded RNART.HDV.CE is intended for the reverse transcription to cDNA of Hepatits delta virus RNA. Reverse transcription polymerase chain reaction (RT-PCR) is aimed to the generation of many copies of a cDNA from an RNA molecule using the enzyme Reverse Transcriptase. The resulting cDNA can be use as template of
- [HDV RNA - PCR](https://www.diapro.it/products/hbv-rna-pcr/) - The HDV Quantitation Real-Time PCR kit coded DRNA.CE is intended for the quantitative detection of Hepatitis D Virus RNA in human serum with a simultaneous control of the amplification reaction through an Internal Control (IC).
- [HBV DNA - PCR](https://www.diapro.it/products/hbv-dna-pcr/) - The HBV DNA Quantitation Real-Time PCR kit coded HBVDNAQT.CE is intended for quantitative detection of Hepatitis B Virus DNA in human plasma with a simultaneous control of the amplification reaction through an Internal Control (IC). The kit is intended for use in conjunction with clinical observation and laboratory markers as an indicator of disease prognosis
- [RNA - PCR](https://www.diapro.it/products/rna-pcr/) - The RNA Retrotrascription kit coded RNART.CE is intended for the reverse transcription to cDNA of highly purified RNA coming from Virus (vRNA) with Random Hexamers. Reverse transcription polymerase chain reaction (RT-PCR) is aimed to the generation of many copies of a cDNA from an RNA molecule using the enzyme Reverse Transcriptase. The resulting cDNA can
- [HSV1 DNA - PCR](https://www.diapro.it/products/hsv1-dna-pcr/) - The HSV1 DNA Quantitation (QT) Real-Time PCR kit coded HSV1DNAQT.CE is intended for the quantitative detection of Human herpes simplex virus 1 DNA in human plasma and CSF (cerebrospinal fluid) with a simultaneous control of the extraction/amplification reaction through an Internal Control (IC).
- [HSV2 DNA - PCR](https://www.diapro.it/products/hsv2-dna-pcr/) - The HSV2 DNA Quantitation (QT) Real-Time PCR kit coded HSV2DNAQT.CE is intended for the quantitative detection of Human herpes simplex virus 2 DNA in human plasma and CSF (cerebrospinal fluid) with a simultaneous control of the extraction/amplification reaction through an Internal Control (IC).
- [EBV DNA - PCR](https://www.diapro.it/products/ebv-dna-pcr/) - The EBV DNA Quantitation (QT) Real-Time PCR kit coded EBVDNAQT.CE is intended for the quantitative detection of Epstein-Barr Virus DNA in human plasma and whole blood collected in EDTA with a simultaneous control of the extraction/amplification reaction through an Internal Control (IC).
- [VZV DNA - PCR](https://www.diapro.it/products/vzv-dna-pcr/) - The VZV DNA Quantitation (QT) Real-Time PCR kit coded VZVDNAQT.CE is intended for the quantitative detection of Varicella-Zoster virus DNA in human plasma and CSF (cerebrospinal fluid) with a simultaneous control of the extraction/amplification reaction through an Internal Control (IC).
- [JCV DNA - PCR](https://www.diapro.it/products/jcv-dna-pcr/) - The JCV DNA Quantitation Real-Time PCR kit coded JCVDNAQT.CE is intended for the quantitative detection of the JC Virus DNA in human plasma ,urine and cerebrospinal fluid (CSF) with a simultaneous control of the amplification/extraction reaction through an Internal Control (IC).
- [COVID-19 RNA Vs 2 - PCR](https://www.diapro.it/products/covid-19-rna-pcr/) - INTENDED USE The Covid-19 RNA Vs 2 Multiplex Real-Time RT-PCR kit coded COV19RNALYO.CE is intended for the specific qualitative detection of SARS-CoV-2 in human samples by simultaneous retrotranscription and amplification of specific target region of Sars-CoV-2 genome (RdRp gene and N gene). In the same reaction tube an endogenous human gene is used as extraction/amplification
- [BKV DNA - PCR](https://www.diapro.it/products/bkv-dna-pcr/) - The BKV DNA Quantitation Real-Time PCR kitcoded BKVDNAQT.CE is intended for the quantitative detection of the BK Virus DNA in human plasma and urine with a simultaneous control of the amplification/extraction reaction through an Internal Control (IC). The kit has been adapted for the use on the Real-Time Thermacyclers ABI 7500 Sequence Detection System® (Software
- [HHV8 DNA - PCR](https://www.diapro.it/products/hhv8-dna-pcr/) - The HHV8 DNA Quantitation (QT) Real-Time PCR kit coded HHV8DNAQT.CE is intended for the quantitative detection of Human herpesvirus 8 DNA in human plasma/blood with a simultaneous control of the extraction/amplification reaction through an Internal Control (IC).
- [HHV6 DNA - PCR](https://www.diapro.it/products/hhv6-dna-pcr/) - The HHV6 DNA Quantitation Real-Time PCR kit coded HHV6DNAQT.CEis intended for the quantitative detection of the Herpesvirus 6 DNA in human plasma/blood with a simultaneous control of the amplification/extraction reaction through an Internal Control (IC).
- [ENTEROVIRUS RNA - PCR](https://www.diapro.it/products/enterovirus-rna-pcr/) - The Enterovirus RNA Real-Time PCR kit coded ENTERORNA.CE is intended for the qualitative detection of Enterovirus RNA in human plasma and CSF samples (Cerebral Spinal Fluid) with a simultaneous control of the amplification reaction through an Internal Control (IC).
- [CMV DNA - PCR](https://www.diapro.it/products/cmv-dna-pcr/) - The CMV DNA Quantitation (QT) 2nd Generation Real-Time PCR kit coded CMVDNAQT.2G.CE is intended for the quantitative detection of Cytomegalovirus DNA in human sample (blood, plasma, amniotic fluid) with a simultaneous control of the extraction/amplification reaction through an Internal Control (IC). CMVDNAQT.2G.CE assay was standardised against the 1st WHO International Standard for HCMV (NIBSC code 09/162) to express
- [DIA.CHEMILUX SARS-CoV-2 Spike/RBD Ab - CLIA](https://www.diapro.it/products/dia-chemilux-sars-cov-2-spike-rbd-ab-clia/) - Chemi-Luminescence ImmunoAssay (CLIA) for the quantitative determination of antibodies to COVID-19 Virus (SARS-CoV-2) Spike/RBD in human plasma and sera. The Antibody assay is intended for testing: (a) health-care workers at risk of COVID-19 infection to verify whether or not they might be positive for potentially neutralizing anti Spike/RBD antibodies. (b) normal population for epidemiology studies
- [DIA.CHEMILUX SARS-CoV-2 ACE2/RBD Neutralization - CLIA](https://www.diapro.it/products/dia-chemilux-sars-cov-2-ace2-rbd-neutralization-clia/) - Chemi-Luminescence ImmunoAssay (CLIA) for the serological determination of the neutralization activity of antibodies to SARS-CoV-2, induced by natural infection and/or vaccination, able to block the interaction of Receptor Binding Domain (RBD) and ACE2 and thus the virus infection. The assay is intended for testing sera and plasma collected from: (a) PCR-negative Covid-19 individuals successfully recovered
- [DIA.CHEMILUX IgM del SARS-CoV-2 NCP - CLIA](https://www.diapro.it/products/dia-chemilux-covid-19-ab/) - Chemi-Luminescence ImmunoAssay (CLIA) for the semi-quantitative determination of IgM antibodies to SARS-CoV-2 Nucleocapsid protein (NCP) in human plasma and sera. The kit is intended for monitoring of infected patients. In addition the kit may be used when testing the population and health-care workers looking for potentially infective “pauci” or a-symptomatic individuals in the early phase
- [DIA.CHEMILUX SARS-CoV-2 NCP IgG - CLIA](https://www.diapro.it/products/dia-chemilux-sars-cov-2-ncp-igg-clia/) - Chemi-Luminescence ImmunoAssay (CLIA) for the semi-quantitative determination of IgG antibodies to SARS-CoV-2 Nucleocapsid protein (NCP) in human plasma and sera. The kit is intended for monitoring of infected patients. In addition the kit may be used when testing the population and health-care workers looking for potentially infective “pauci” or a-symptomatic individuals in the early phase
- [DIA.CHEMILUX SARS-CoV-2 NCP IgA - CLIA](https://www.diapro.it/products/dia-chemilux-sars-cov-2-ncp-iga-clia/) - Chemi-Luminescence ImmunoAssay (CLIA) for the quantitative determination of IgA antibodies to SARS-CoV-2 Nucleocapsid protein (NCP) in human plasma and sera. The kit is intended for monitoring of infected patients. In addition, the kit may be used when testing the population and health-care workers looking for potentially infective “pauci” or a-symptomatic individuals in the early phase
- [DIA.CHEMILUX IgG anti-JO1 - CLIA](https://www.diapro.it/products/dia-chemilux-igg-anti-jo1-clia/) - Chemi-Luminescence ImmunoAssay (CLIA) for the quantitative determination of IgG antibodies to JO-1 autoantigens in human plasma and sera. The device is intended to be used in combination only with the fully automated Random Access platform SARA.
- [DIA.CHEMILUX IgG anti-RNP - CLIA](https://www.diapro.it/products/dia-chemilux-igg-anti-rnp-clia/) - Chemi-Luminescence ImmunoAssay (CLIA) for the quantitative determination of IgG antibodies to U1-snRNP 68 autoantigens in human plasma and sera.The device is intended to be used in combination only with the fully automated Random Access platform.
- [DIA.CHEMILUX IgG anti-SCL70 - CLIA](https://www.diapro.it/products/dia-chemilux-igg-anti-scl70-clia/) - Chemi-Luminescence ImmunoAssay (CLIA) for the quantitative determination of IgG antibodies to Scl70 autoantigens in human plasma and sera.The device is intended to be used in combination only with the fully automated Random Access platform.
- [DIA.CHEMILUX IgG anti-SSA52 - CLIA](https://www.diapro.it/products/dia-chemilux-igg-anti-ssa52-clia-2/) - Chemi-Luminescence ImmunoAssay (CLIA) for the quantitative determination of IgG antibodies to SSA 52 autoantigens in human plasma and sera.The device is intended to be used in combination only with the fully automated Random Access platform SARA.
- [DIA.CHEMILUX IgG anti-Sm - CLIA](https://www.diapro.it/products/dia-chemilux-igg-anti-ssa52-clia/) - Chemi-Luminescence ImmunoAssay (CLIA) for the quantitative determination of IgG antibodies to SM autoantigens in human plasma and sera. The device is intended to be used in combination only with the fully automated Random Access platform SARA.
- [DIA.CHEMILUX IgG anti-SSB - CLIA](https://www.diapro.it/products/dia-chemilux-igg-anti-ssb-clia/) - Chemi-Luminescence ImmunoAssay (CLIA) for the quantitative determination of IgG antibodies to SSB autoantigens in human plasma and sera. The device is intended to be used in combination only with the fully automated Random Access platform SARA
- [CHIKV IgM - ELISA](https://www.diapro.it/products/chikv-igm-elisa/) - Enzyme ImmunoAssay (ELISA) for the qualitative determination of IgM antibodies to Chikungunya Virus (CHIKV) in human plasma and sera collected from patients suspected of an ongoing Chikungunya Virus infection or at risk of it. The kit is intended for the diagnosis of acute infection in CHIKV infected patients.
- [CHIKV IgG - ELISA](https://www.diapro.it/products/chikv-igg-elisa/) - Enzyme ImmunoAssay (ELISA) for the qualitative and semi quantitative determination of IgG antibodies to Chikungunya Virus (CHIKV) in human plasma and sera. The kit is intended for the follow-up of CHIKV-infected patients.
- [HCV IgM - ELISA](https://www.diapro.it/products/hcv-igm-elisa/) - Enzyme ImmunoAssay (ELISA) for the quantitative/qualitative determination of IgM antibodies to Hepatitis C Virus in human plasma and sera. The kit is mainly intended for the follow-up of HCV chronic patients submitted to anti-viral pharmaceutical treatment.

## Categories

- [Blog](https://www.diapro.it/category/blog/)

## Tags

- [ELISA](https://www.diapro.it/tag/elisa/)
- [Dengue virus](https://www.diapro.it/tag/dengue-virus/)
- [mosquitoes](https://www.diapro.it/tag/mosquitoes/)
- [infection](https://www.diapro.it/tag/infection/)
- [anti-dengue antibodies](https://www.diapro.it/tag/anti-dengue-antibodies/)
- [tropical diseases](https://www.diapro.it/tag/tropical-diseases/)
- [Serological methods](https://www.diapro.it/tag/serological-methods/)
- [Chikungunya](https://www.diapro.it/tag/chikungunya/)
- [Zika](https://www.diapro.it/tag/zika/)
- [MADE IN ITALY](https://www.diapro.it/tag/made-in-italy/)
- [LOCAL MANUFACTURER](https://www.diapro.it/tag/local-manufacturer/)
- [EXPORT](https://www.diapro.it/tag/export/)
- [ITALIAN EXCELLENCE](https://www.diapro.it/tag/italian-excellence/)
- [CHAMPION](https://www.diapro.it/tag/champion/)
- [CITATION](https://www.diapro.it/tag/citation/)
- [Malaria](https://www.diapro.it/tag/malaria/)
- [WestNile](https://www.diapro.it/tag/westnile/)
- [Yellow Fever](https://www.diapro.it/tag/yellow-fever/)
- [Chagas](https://www.diapro.it/tag/chagas/)
- [Vector-Borne Diseases](https://www.diapro.it/tag/vector-borne-diseases/)
- [CLIA](https://www.diapro.it/tag/clia/)
- [BLOOD SCREENING](https://www.diapro.it/tag/blood-screening/)

## Panel Categories

- [ELISA](https://www.diapro.it/panel_cat/elisa/)
- [RT.PCR](https://www.diapro.it/panel_cat/rt-pcr/)
- [CLIA](https://www.diapro.it/panel_cat/clia/)
- [Blood Screening](https://www.diapro.it/panel_cat/blood-screening/)
- [Hepatitis](https://www.diapro.it/panel_cat/hepatitis/)
- [Tropical Diseases](https://www.diapro.it/panel_cat/tropical-diseases/)
- [TORCH](https://www.diapro.it/panel_cat/torch/)
- [Serology](https://www.diapro.it/panel_cat/serology/)
- [Autoimmunity](https://www.diapro.it/panel_cat/autoimmunity/)
- [Trasplantation](https://www.diapro.it/panel_cat/trasplantation/)
- [COVID-19](https://www.diapro.it/panel_cat/covid-19/)

## Panel Tags

- [blood_screening_elisa](https://www.diapro.it/panel_tag/blood_screening_elisa/)
- [hepatits_elisa](https://www.diapro.it/panel_tag/hepatits_elisa/)
- [tropical_diseases_elisa](https://www.diapro.it/panel_tag/tropical_diseases_elisa/)
- [torch_elisa](https://www.diapro.it/panel_tag/torch_elisa/)
- [serology_elisa](https://www.diapro.it/panel_tag/serology_elisa/)
- [autoimmunity_elisa](https://www.diapro.it/panel_tag/autoimmunity_elisa/)
- [covid19_elisa](https://www.diapro.it/panel_tag/covid19_elisa/)
- [blood_screening_clia](https://www.diapro.it/panel_tag/blood_screening_clia/)
- [tropical_diseases_clia](https://www.diapro.it/panel_tag/tropical_diseases_clia/)
- [torch_clia](https://www.diapro.it/panel_tag/torch_clia/)
- [serology_clia](https://www.diapro.it/panel_tag/serology_clia/)
- [autoimmunity_clia](https://www.diapro.it/panel_tag/autoimmunity_clia/)
- [covid19_clia](https://www.diapro.it/panel_tag/covid19_clia/)
- [covid19_pcr](https://www.diapro.it/panel_tag/covid19_pcr/)
- [hepatits_pcr](https://www.diapro.it/panel_tag/hepatits_pcr/)
- [serology_pcr](https://www.diapro.it/panel_tag/serology_pcr/)
- [trasplantation_pcr](https://www.diapro.it/panel_tag/trasplantation_pcr/)

## Product Categories

- [Product](https://www.diapro.it/product_cat/product/)

## Product Tags

- [Syphilis](https://www.diapro.it/product_tag/syphilis/)