0.312-20ng/ml

0.136ng/ml

The microtiter plate provided in this kit has been pre-coated with an antibody specific to FOXO1. Standards or samples are then added to the appropriate microtiter plate wells with a biotin-conjugated antibody specific to FOXO1. Next, Avidin conjugated to Horseradish Peroxidase (HRP) is added to each microplate well and incubated. After TMB substrate solution is added, only those wells that contain FOXO1, biotin-conjugated antibody and enzyme-conjugated Avidin 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 FOXO1 in the sample is then determined by comparing the O.D. of the sample to the standard curve.

*025150A: Microtiter Plate, 1x96 wells, Pre-coated; ready to use *025150B: Standard, 2x1vial 025150C: Standard Diluent, 1x20ml *025150D: Detection Reagent A, 1x120ul *025150E: Detection Reagent B, 1x120ul 025150F: Assay Diluent A, 1x12ml 025150G: Assay Diluent B, 1x12ml 025150H: TMB Substrate, 1x9ml 025150K: Stop Solution, 1x6ml 025150L: Wash Buffer, 30X, 1x20ml

Store *025150A, *025150B, *025150D and *025150E at -20°C. Store all the other components at 4°C. Unused kit is stable for 6 months. Once kit components are opened, it is highly recommended to use remaining reagents within 1 month provided this is within the expiration date of the kit. For maximum recovery of product, centrifuge the original vials after thawing and prior to removing the cap.

1. Prepare all reagents, samples and standards. 2. Add 100ul standard or sample to each well. Incubate 2 hours at 37°C. 3. Aspirate and add 100ul prepared Detection Reagent A. Incubate 1 hour at 37°C. 4. Aspirate and wash 3 times. 5. Add 100ul prepared Detection Reagent B. Incubate 30 minutes at 37°C. 6. Aspirate and wash 5 times. 7. Add 90ul TMB Substrate. Incubate 15-25 minutes at 37°C. 8. Add 50ul Stop Solution. Read at 450nm immediately.