Troponin T Type 2, Cardiac (TNNT2) BioAssay™ ELISA Kit (Rat)
|Kits and Assays||Storage: 4°C/-20°CShipping: Blue Ice|
The Rat Cardiac Troponin T, Type 2 (TNNT2) ELISA Kit is a sandwich enzyme immunoassay for the in vitro quantitative measurement of TNNT2 in rat serum, plasma and other biological fluids.
The microtiter plate provided in this kit has been pre-coated with an antibody specific to TNNT2. Standards or samples are then added to the appropriate microtiter plate wells with a biotin-conjugated antibody specific to TNNT2. 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 TNNT2, 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 TNNT2 in the sample is then determined by comparing the O.D. of the sample to the standard curve.
*028637A: Microtiter Plate, 1x96 wells, Pre-coated; ready to use
*028637B: Standard, 2x1vial
028637C: Standard Diluent, 1x20ml
*028637D: Detection Reagent A, 1x120ul
*028637E: Detection Reagent B, 1x120ul
028637F: Assay Diluent A, 1x12ml
028637G: Assay Diluent B, 1x12ml
028637H: TMB Substrate, 1x9ml
028637K: Stop Solution, 1x6ml
028637L: Wash Buffer, 30x, 1x20ml
Storage and Stability:
Store *028637A, *028637B, *028637D and *028637E 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.
Assay Procedure Summary:
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.
Important Note: This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications without the expressed written authorization of United States Biological.