Rat MSRA ELISA KIT
Packing 96Tests
FOR RESEARCH USE ONLY; NOT FOR THERAPEUTIC OR DIAGNOSTIC APPLICATIONS! PLEASE READ ENTIRE PROCEDURE!
Gene Name MSRA
Protein Name Mitochondrial peptide methionine sulfoxide reductase
Alternative Name
Rat MSRA ELISA KIT ,Rat mitochondrial peptide methionine sulfoxide reductase ELISA KIT ,Rat PMSR ELISA KIT ,Rat cytosolic methionine-S-sulfoxide reductase ELISA KIT ,Rat peptide Met(O) reductase ELISA KIT ,Rat peptide met (O) reductase ELISA KIT ,Rat peptide-methionine (S)-S-oxide reductase ELISA KIT ,Rat methionine sulfoxide reductase A ELISA KIT
Intended use
Rat MSRA ELISA KIT allows for the in vitro quantitative determination of MSRA 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 MSRA ELISA KIT has been pre-coated with an MSRA antibody specific to MSRA. Standards or samples are then added to the appropriate microtiter plate wells with a biotin-conjugated antibody preparation specific for MSRA 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 MSRA, 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 MSRA 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