DPYD Mutations Detection Ki
Dihydropyrimidine dehydrogenase (DPD) is an enzyme encoded by the DPYD gene and is involved in the metabolism of fluoropy- rimidines, chemotherapeutics used in the treatment of some solid tumors.
Learn moreHLA-B*51 Detection Kit (Behcet's Disease)
The HLA-B*51 allele, a class I human leukocyte antigen (HLA) molecule, is the strongest known genetic risk factor for Behçet's Disease (BD).
Learn moreHLA-B*27 Detection Kit (Ankylosing Spondylitis)
HLA-B*27 is a genetic risk factor for seronegative spondyloarthropathies, such asankylosing spondylitis, reactive arthritis, juvenile rheumatoid arthritis and anterior uveitis.
Learn moreFII Mutation Detection Kit
FII Mutation Detection Kit is a rapid and accurate, real-time PCR-based assay for the detection of the 20210G>A mutation in the human Factor II (F2) gene encoding the clotting factor prothrombin (PTH).
Learn moreCeliac (DQ2, DQ8, DR4) Detection Kit
Celiac disease is a common, familial, autoimmune gastrointestinal disease. It is caused by sensitivity to the dietary protein gluten, which is present in wheat, rye, and barley.
Learn moreFV Leiden Mutation Detection Kit
The FV Leiden mutation is associated with inherited thrombophilia. The kit is designed to identify patients at risk of venous thromboembolism. 20-50% of patients with VTE have this mutation.
Learn moreThrombophilia Panel, 50T (FII, FVL, MTHFR 677, MTHFR1298)
Thrombophilia, a condition with an increased risk of blood clotting, is linked to venous thromboembo- lism (VTE).
Learn moreMTHFR C677T/A1298C
This kit detects MTHFR C677T and A1298C Mutations in Huma Oral Swab or whole blood.
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