Control Materials for Verifying Reproducibility and Accuracy of Qualitative Detection of IgG Antibodies to Hepatitis A Virus Using Chemiluminescent Immunoassay on Alinity i Analyzers

Control Materials for Verifying Reproducibility and Accuracy of Qualitative Detection of IgG Antibodies to Hepatitis A Virus Using Chemiluminescent Immunoassay on Alinity i Analyzers

Control materials are used to confirm the reproducibility and accuracy of qualitative detection of IgG antibodies to the hepatitis A virus in human serum and plasma by chemiluminescent immunoassay on Alinity i immunochemical analyzers.

Contents:

• Positive Control (Alinity i HAVAb IgG Control +) – 1 vial x 8 ml
• Negative Control (Alinity i HAVAb IgG Control -) – 1 vial x 8 ml
• Instructions for use

Reagent Kit for Qualitative Detection of IgG Antibodies to Hepatitis A Virus by Chemiluminescent Immunoassay in Human Serum and Plasma on Alinity i Analyzers

The reagent kit is designed for qualitative detection of IgG antibodies to the hepatitis A virus using chemiluminescent immunoassay in serum and plasma samples with Alinity i immunoassay analyzers.

Kit Versions:

2-Cartridge Kit for 100 Tests:

• Microparticles (Alinity i HAVAb IgG Microparticles) – 2 x 6.6 ml
• Conjugate (Alinity i HAVAb IgG Conjugate) – 2 x 26.5 ml
• Assay Diluent (Alinity i HAVAb IgG Assay Diluent) – 2 x 10.4 ml
• Instructions for use

2-Cartridge Kit for 500 Tests:

• Microparticles (Alinity i HAVAb IgG Microparticles) – 2 x 27.0 ml
• Conjugate (Alinity i HAVAb IgG Conjugate) – 2 x 26.5 ml
• Assay Diluent (Alinity i HAVAb IgG Assay Diluent) – 2 x 47.1 ml
• Instructions for use

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The products posted on our website are approved for use in Russia by the state regulator Roszdravnadzor (Federal Service for Surveillance in Healthcare). The information is for informational purposes only.