Rat alpha 1 Acid Glycoprotein/AGP ELISA kit is a sandwich Enzyme-Linked Immunosorbent Assay (sELISA) designed for the in vitro quantitative determination of rat alpha 1 Acid Glycoprotein/AGP in serum, plasma, tissue homogenates, and other biological fluids.

• Ready To Use ELISA Kit
• Detection Range: 6.25 to 400 ng/ml
• Sensitivity: 3.75 ng/ml
• Sample Type: Serum, plasma, tissue homogenates, and other biological fluids
• Assay Precision: Intra - Assay: CV <8%, Inter - Assay: CV <10%

Rat alpha 1 Acid Glycoprotein / AGP ELISA Kit (A77521) employs the sandwich enzyme immunoassay technique for the quantitative measurement of rat alpha 1 Acid Glycoprotein / AGP in serum, plasma, tissue homogenates, and other biological fluids. An antibody specific for alpha 1 Acid Glycoprotein / AGP has been pre-coated onto a 96-well microtiter plate. The standards and test samples are added into the wells and the alpha 1 Acid Glycoprotein / AGP present in each sample is bound to the wells by the immobilized antibody. Following incubation, the wells are washed and then incubated with Biotinylated Anti-alpha 1 Acid Glycoprotein / AGP Antibody, which binds the captured alpha 1 Acid Glycoprotein / AGP present in each well. Following incubation, unbound biotinylated detection antibody is removed by washing, and an HRP-Streptavidin conjugate is added to the wells and the microtiter plate is incubated. Following incubation and washing, TMB substrate solution is then used to visualize the HRP enzymatic reaction by catalysis to produce a blue-coloured product that changes to yellow after addition of acidic stop solution. The density of yellow is proportional to the amount of alpha 1 Acid Glycoprotein / AGP captured in each well. The concentration of alpha 1 Acid Glycoprotein / AGP can then be calculated by reading the O.D. absorbance at 450nm in a microplate reader and referring to the standard curve.