Rat IgA ELISA Assay
The Rat IgA ELISA Assay is For Research Use Only
Size: 1×96 wells
Sensitivity: 7.938 ng/ml
Dynamic Range: 31.25 ng/ml – 1000 ng/ml
Incubation Time: 70 minutes
Sample Type: Plasma, Serum, Urine
Sample Size: 100 µL
Assay Principle for Rat IgA ELISA
The principle of the double antibody sandwich ELISA is represented in Figure 1. In this assay the rat IgA present in samples reacts with the anti-IgA antibodies which have been adsorbed to the surface of polystyrene microtitre wells. After the removal of unbound proteins by washing, anti-IgA antibodies conjugated with horseradish peroxidase (HRP), are added. These enzyme-labeled antibodies form complexes with the previously bound IgA. Following another washing step, the enzyme bound to the immunosorbent is assayed by the addition of a chromogenic substrate, 3,3’,5,5’-tetramethylbenzidine (TMB). The quantity of bound enzyme varies directly with the concentration of rat IgA in the sample tested; thus, the absorbance, at 450 nm, is a measure of the concentration of IgA in the test sample. The quantity of rat IgA in the test sample can be interpolated from the standard curve constructed from the standards, and corrected for sample dilution.
SPECIMEN COLLECTION AND HANDLING
Blood should be collected by venipuncture. The serum should be separated from the cells after clot formation by centrifugation. For plasma samples, blood should be collected into a container with an anticoagulant and then centrifuged. Care should be taken to minimize hemolysis, excessive hemolysis can impact your results. Assay immediately or aliquot and store samples at -20°C. Avoid repeated freeze thaw cycles.
