Description |
The AKR1B1 (Aldose Reductase) BioAssay™ ELISA Kit (Human) is a quantitative sandwich assay for the detection of AKR1B1 in human serum, plasma and other biological fluids. Cell lysates and tissue homogenates, though not tested, may potentially be used as samples.
Detection Range: 0.156-10ng/ml
Sensitivity: <0.094ng/ml
Precision: Intra-Assay CV: <8% Inter-Assay CV: <10%
Assay Principle: The microtiter plate provided in this kit has been pre-coated with an antibody specific to AKR1B1. Standards and samples are added to the appropriate microtiter plate wells followed by a biotin-conjugated antibody specific to AKR1B1. Streptavidin conjugated to horseradish peroxidase (HRP) is added to each microplate well and incubated. After TMB substrate solution is added, only those wells that contain AKR1B1, biotin-conjugated antibody and enzyme-conjugated streptavidin complex will exhibit a change in color. The enzyme-substrate reaction is terminated by the addition of sulfuric acid solution and the color change is measured spectrophotometrically at a wavelength of 450nm ± 10nm. The concentration of AKR1B1 in the sample is then determined by comparing the O.D. of the sample to the standard curve.
Kit Components: *353811A: Microtiter Strips, 8x12 wells. *353811B: Standard, 2 vials 353811C: Sample/Standard Dilution Buffer, 1x20ml 353811D: Antibody-Biotin (Concentrated), 1x120ul 353811E: Antibody Dilution Buffer, 1x10ml *353811F: Streptavidin-HRP Conjugate (SABC), 1x120ul 353811G: SABC Dilution Buffer, 1x10ml *353811H: TMB Substrate, 1x10ml 353811J: Stop Solution, 1x10ml 353811K: Wash Buffer (25X), 1x30ml
Storage and Stability: Store unopened *353811A at 4ºC; store at -20ºC once opened. Store unopened *353811B at 4°C; once reconstituted store at 4°C for up to 12 hours or at -20°C for up to 48 hours. Store *353811F and *353811H in the dark at 4°C. Store all other components at 4°C. Kit is stable for 6 months after receipt. For maximum recovery of product, centrifuge the original vials after thawing and prior to removing the cap.
Assay Summary: 1. Wash plate 2 times before adding standards, samples and control (zero) to wells. 2. Add 100ul standard or sample to each well and incubate for 90 minutes at 37°C 3. Aspirate the liquid and wash plate 3 times. 3. Add 100ul Antibody-Biotin working solution to each well and incubate for 60 minutes at 37°C 4. Aspirate the liquid and wash plate 3 times. 5. Add 100ul SABC working solution to each well. Incubate for 30 minutes at 37°C 6. Aspirate the liquid and wash plate 5 times. 7. Add 90ul TMB substrate. Incubate 15-30 minutes at 37°C 8. Add 50ul Stop Solution. Read at 450nm immediately. 9. Calculate results. |