This Heparan Sulfate (HS) BioAssay™ ELISA Kit is a sandwich ELISA for the in vitro quantitative determination of Heparan Sulfate concentrations in human serum, plasma and other biological fluids.
Specificity:Recognizes human Heparan Sulfate. No Significant cross-reactivity or interference between human Heparan Sulfate and analogues was observed.
Test Principle:The micro ELISA plate provided in this kit has been pre-coated with an antibody specific to human Heparan Sulfate. Standards or samples are added to the micro ELISA plate wells and combined with the specific antibody. Then a biotinylated detection antibody specific for human Heparan Sulfate and Avidin-Horseradish Peroxidase (HRP) conjugate are added successively to each micro plate well and incubated. Free components are washed away. The substrate solution is added to each well. Only those wells that contain human Heparan Sulfate, biotinylated detection antibody and Avidin-HRP conjugate will appear blue in color. The enzyme-substrate reaction is terminated by the addition of stop solution and the color turns yellow. The optical density (O.D.) is measured spectrophotometrically at a wavelength of 450nm ± 2nm. The O.D. value is proportional to the concentration of human Heparan Sulfate. You can calculate the concentration of human Heparan Sulfate in the samples by comparing the O.D. of the samples to the standard curve.
Storage and Stability:Store *529991A, *529991B, *529991D and *529991E at -20°C. 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.
Assay Procedure Summary:1. Prepare all reagents, samples and standards
2. Add 100ul standard or sample to each well. Incubate 90 minutes at 37°C
3. Aspirate and add 100ul prepared Biotin Working Solution. Incubate 1 hour at 37°C
4. Aspirate and wash 3 times
5. Add 100ul prepared HRP Detection Working Solution. Incubate 30 minutes at 37°C
6. Aspirate and wash 5 times
7. Add 90ul Substrate. Incubate 15 minutes at 37°C
8. Add 50ul Stop Solution. Read at 450nm immediately.
