Rat LTA4H ELISA KIT
Packing 96Tests
FOR RESEARCH USE ONLY; NOT FOR THERAPEUTIC OR DIAGNOSTIC APPLICATIONS! PLEASE READ ENTIRE PROCEDURE!
Gene Name LTA4H
Protein Name leukotriene A4 hydrolase
Alternative Name
Rat LTA4H ELISA KIT ,Rat leukotriene A4 hydrolase ELISA KIT ,Rat leukotriene A-4 hydrolase ELISA KIT ,Rat LTA-4 hydrolase ELISA KIT ,Rat testicular secretory protein Li 27 ELISA KIT
Intended use
Rat LTA4H ELISA KIT allows for the in vitro quantitative determination of LTA4H 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 LTA4H ELISA KIT has been pre-coated with an LTA4H antibody specific to LTA4H. Standards or samples are then added to the appropriate microtiter plate wells with a biotin-conjugated antibody preparation specific for LTA4H 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 LTA4H, 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 LTA4H 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