Hepatitis D virus Antigen (HDV-Ag) ELISA Kit
Principle:
This kit employs the double-antibody sandwich enzyme-linked immunosorbent assay (ELISA) principle to detect hepatitis D virus antigen (HDV-Ag) in human serum or plasma samples. The polystyrene microwell strips are pre-coated with anti-HDV antibodies (capture antibodies). Upon addition of the serum or plasma specimen along with a lysis solution (to facilitate antigen release if applicable), any HDV-Ag present in the sample binds specifically to the immobilized capture antibodies during incubation. Subsequently, horseradish peroxidase (HRP)-conjugated anti-HDV antibodies (detection antibodies) are added, which bind to a different epitope on the captured HDV-Ag, forming a (capture Ab) - HDV-Ag - (HRP-detection Ab) sandwich complex. Following a wash step to remove unbound HRP conjugates and other components, a chromogenic substrate (TMB) is added to the wells. In the presence of the immunocomplex, the HRP enzyme catalyzes the substrate reaction, producing a blue color proportional to the amount of HDV-Ag. The reaction is terminated by adding a stop solution (typically 50 μL per well), which changes the color to yellow. The absorbance (optical density) is then measured using a microplate reader at the appropriate wavelength (e.g., 450 nm) to determine the presence and concentration of HDV-Ag in the sample.
Product Features:
High sensitivity, specificity and stability







