E01I0005 Human Inhibin B ELISA kit
The Human Inhibin B ELISA kit can be used to identify samples from the human species. Inhibin B can also be called INB, INHB, INH-B, Inhibin B.
Human Inhibin B ELISA kit
48 Tests / 96 Tests
Serum, plasma, cell culture supernatants, body fluid and tissue homogenate
STANDARD A (0.5mL)
STANDARD B (0.5mL)
STANDARD C (0.5mL)
STANDARD D (0.5mL)
STANDARD E (0.5mL)
STANDARD F (0.5mL)
WASH SOLUTION (100 x)
Principle of the Assay
INB ELISA kit uses an anti-INB antibody and an INB-HRP conjugate in a competitive enzyme immunoassay method. INB-HRP conjugate is incubated with the assay sample and buffer in a pre-coated plate for one hour. The wells are decanted and washed five times when the incubation period is over. The HRP enzyme substrate is then incubated in the wells. The result of the enzyme-substrate reaction is a complex that is blue in hue. The process is finally stopped by adding a stop solution, causing the solution to turn yellow. In a microplate reader, the color intensity is measured spectrophotometrically at 450 nm. Due to competition for the anti-INB antibody binding site between INB from samples and INB-HRP conjugate, the intensity of the color is inversely proportional to the concentration of INB. Since the number of sites is limited, as more sites are occupied by INB from the sample, fewer sites are left to bind INB-HRP conjugate. A standard curve is plotted relating the intensity of the color (O.D.) to the concentration of standards. The INB concentration in each sample is interpolated from this standard curve.
Coefficient of Variance
Intra Variation% ＜10%
Inter Variation% ＜12%
No significant cross-reactivity or interference between INB and analogues was observed.
E01I0005 has been referenced in the below publications：
Post-chemotherapy serum anti-Müllerian hormone level predicts ovarian function recovery.
Application of non-invasive detection of peripheral vascular dysfunction in ovarian hyperstimulation syndrome (OHSS): A pilot study of clinical relevance.
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