The Thrombospondin 1 (THBS1) High Sensitivity BioAssay™ ELISA Kit is a sandwich enzyme immunoassay for the in vitro quantitative measurement of THBS1 in mouse plasma, tissue homogenates and other biological fluids.
Detection Range:62.5-4000pg/ml
Sensitivity:26.7pg/ml
Intra-Assay CV:<10%
Inter-Assay CV:<12%
Kit Components:*517695A: Microtiter Plate, 1x96 wells, Pre-coated, ready to use
Precaution:The Stop Solution (517695K) included for use in this kit is an acid solution. Wear eye, hand, face, and clothing protection when using this material.
Storage and Stability:Store *517695A, *517695B, *517695D, *517695E and *517695J at -20°C. After reconstitution of *5176958, store at 4°C and use within 5 days. Store all the other components at 4°C. Unused kit is stable for 6 months after receipt. 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.
Notes on 517508J: Positive Control
Intended Use:The positive control is from a mouse plasma 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.
Characteristics:The positive control vial contains mouse THBS1 in mouse plasma (lyophilized powder). Note: The mouse based serum used in this product are from healthy mouse of SPF standard (Specific Pathogen-Free animals).
Expected Values:314.8pg/ml
Usage:Dissolve with 150ul standard diluent 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: Upon receipt store Positive Control vial at -20°C. After reconstitution, store Positive Control vial at 4°C and use within 5 days.
Assay Procedure Summary:1. Prepare all reagents, samples and standards
2. Add 100ul standard or sample to each well. Incubate 1 hour 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 Substrate Solution. Incubate 10-20 minutes at 37°C
8. Add 50ul Stop Solution. Read at 450nm immediately
