Hepatitis G virus IgG (HGV-IgG) ELISA Kit
Principle:
This kit employs the indirect enzyme-linked immunosorbent assay (ELISA) principle to detect hepatitis G virus IgG antibodies (anti-HGV IgG, primarily directed against the envelope glycoprotein E2) in human serum or plasma samples. The polystyrene microwell strips are pre-coated with recombinant hepatitis G virus (HGV) antigens. Upon addition of the serum or plasma specimen, any anti-HGV IgG antibodies present in the sample bind specifically to the immobilized antigens, while unbound components are removed by washing. In the subsequent step, horseradish peroxidase (HRP)-conjugated mouse anti-human IgG antibodies are added, which bind to the captured human IgG. Following another wash to remove unbound HRP conjugates, a chromogenic substrate (TMB) is added to the wells. In the presence of the antigen - anti-HGV IgG - HRP-anti-human IgG immunocomplex, the HRP enzyme catalyzes the substrate reaction, producing a blue color that is proportional to the concentration of anti-HGV IgG. The reaction is halted by adding a stop solution (typically 50 μL per well), which shifts the color to yellow. The absorbance (optical density) is then measured using a microplate reader at the appropriate wavelength (e.g., 450 nm, with a reference wavelength of 620-690 nm if required) to determine the presence and level of anti-HGV IgG antibodies in the sample.
Product Features:
High sensitivity, specificity and stability







