Sample Type:|Serum, plasma, tissue homogenates, cell lysates, cell culture supernates and other biological fluids||Intended Use:|The kit is a competitive inhibition enzyme immunoassay technique for the in vitro quantitative measurement of VB2 in serum, plasma, tissue homogenates, cell lysates, cell culture supernates and other biological fluids.||Sensitivity:|2.55ng/ml||Range:|7.41-600ng/ml||Specificity:|This assay has high sensitivity and excellent specificity for detection of Vitamin B2 (VB2). No significant cross-reactivity or interference between Vitamin B2 (VB2) and analogues was observed.||Precision:|Intra-Assay: CV<10% |Inter-Assay: CV<12%||Test Principle:|This assay employs the competitive inhibition enzyme immunoassay technique. A monoclonal antibody specific to VB2 has been pre-coated onto a microplate. A competitive inhibition reaction is launched between biotin labeled VB2 and unlabeled VB2 (Standards or samples) with the pre-coated antibody specific to VB2. After incubation the unbound conjugate is washed off. Next, avidin conjugated to Horseradish Peroxidase (HRP) is added to each microplate well and incubated. The amount of bound HRP conjugate is reverse proportional to the concentration of VB2 in the sample. After addition of the substrate solution, the intensity of color developed is reverse proportional to the concentration of VB2 in the sample.||Kit Components:|96-well strip plate, 1x Plate |Standard, 2x vial|Detection Reagent A, 1|Detection Reagent B, 1×120ul|Reagent Diluent, 1×300ul|TMB Substrate, 1×9ml|Wash Buffer (30X), 1×20ml|Standard Diluent, 1×20ml|Assay Diluent A, 1×12ml|Assay Diluent B, 1×12ml|Stop Solution, 1x6ml||Storage and Stability:|Store all components at 4°C. Stable for 6 months after receipt. For maximum recovery of product, centrifuge the original vial after thawing and prior to removing the cap.

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