Rat GSR ELISA KIT
Packing 96Tests
FOR RESEARCH USE ONLY; NOT FOR THERAPEUTIC OR DIAGNOSTIC APPLICATIONS! PLEASE READ ENTIRE PROCEDURE!
Gene Name GSR
Protein Name GSR mitochondrial
Rat GSR ELISA KIT Detection Range
Alternative Name
Rat GSR ELISA KIT ,Rat GSR mitochondrial mitochondrial ELISA KIT ,Rat HEL-75 ELISA KIT ,Rat HEL-S-122m ELISA KIT ,Rat GRase ELISA KIT ,Rat epididymis luminal protein 75 ELISA KIT ,Rat epididymis secretory sperm binding protein Li 122m ELISA KIT ,Rat glutathione S-reductase ELISA KIT ,Rat glutathione-disulfide reductase ELISA KIT ,Rat GR ELISA KIT ,Rat GSR ELISA KIT
Intended use
Rat GSR ELISA KIT allows for the in vitro quantitative determination of GSR concentrations in serum, plasma, tissue homogenates, cell culture supernates or other biological fluids.
Reagent | Quantity |
Assay plate | 1 |
Standard | 2 |
Sample Diluent | 1 × 20mL |
Assay Diluent A | 1 × 10mL |
Assay Diluent B | 1 × 10mL |
Detection Reagent A | 1 × 120μL |
Detection Reagent B | 1 × 120μL |
Wash Buffer(25 x concentrate) | 1 × 30mL |
Substrate | 1 × 10mL |
Stop Solution | 1 × 10mL |
Plate sealer | 5 |
Test principle
The microtiter plate provided in Rat GSR ELISA KIT has been pre-coated with an GSR antibody specific to GSR. Standards or samples are then added to the appropriate microtiter plate wells with a biotin-conjugated antibody preparation specific for GSR and then avidin conjugated to Horseradish Peroxidase (HRP) is added to each microplate well and incubated. Then a TMB substrate solution is added to each well. Only those wells that contain GSR, biotin-conjugated antibody and enzyme-conjugated Avidin will exhibit a change in color. The enzyme-substrate reaction is terminated by the addition of a sulphuric acid solution and the color change is measured spectrophotometrically at a wavelength of 450 nm ± 2 nm. The concentration of GSR in the samples is then determined by comparing the O.D. of the samples to the standard curve.
Sample collection and storage
Serum - Use a serum separator tube (SST) and allow samples to clot for 30 minutes before centrifugation for 15 minutes at approximately 1000 × g. Remove serum and assay immediately or aliquot and store samples at -20