125-8000pg/ml

≤49pg/ml

CV <10%

CV <12%

*027938A: Microtiter Plate, 1x96 wells, Pre-coated, ready to use *027938B: Standard, 2x1vial  027938C: Standard Diluent, 1x20ml *027938D: Detection Reagent A, 1x120ul  *027938E: Detection Reagent B, 1x120ul  027938F: Assay Diluent A, 1x12ml 027938G: Assay Diluent B, 1x12ml 027938H: TMB Substrate, 1x9ml *027938J: Positive Control, 471.2pg/ml, 1x1vial 027938K: Stop Solution, 1x6ml 027938L: Wash Buffer, 30X, 1x20ml

The Stop Solution (027938K) suggested for use with this kit is an acid solution. Wear eye, hand, face, and clothing protection when using this material.

The control vial is from a human serum sample known to contain the target protein. It will provide a positive result in the ELISA assay, which indicates that the kit is optimized and working properly.

The control vial contains human S100A7 in human serum (lyophilized powder). Note: The human based material used in this product are screened for HIV, Hepatitis A, B.C, HTLV and Syphilis.

471.2ng/ml

Dissolve with 150ul standard dilutent and let stand for 10 minutes. If powder is partly insoluble, shake gently until fully dissolved. Mix gently before use. In the experiment, add 100ul to an appropriate well of the plate and test its concentration along with standards and your specimens. Note: After reconstitution, store Positive Control vial at 4°C and use within 5 days.

Store *027938A, *027938B, *027938D, *027938E and *027938J at -20°C. After reconstitution of *027938J, store at 4°C and use within 5 days. 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. 4. Add 100ul prepared Detection Reagent B. Incubate 30 minutes at 37°C. 5. Aspirate and wash 5 times. 6. Add 90ul TMB Substrate. Incubate 15-25 minutes at 37°C. 7. Add 50ul Stop Solution. Read at 450nm immediately.