Mouse Phospholipid scramblase 1, PLSCR1 ELISA Kit
96 Tests
Operating instruction
FOR RESEARCH USE ONLY; NOT FOR THERAPEUTIC OR DIAGNOSTIC APPLICATIONS!PLEASE READ THROUGH ENTIRE PROCEDURE BEFORE BEGINNING!
Synonyms
PLSCR ,MmTRA1b,Ca(2+)-dependent phospholipid scramblase 1,Erythrocyte phospholipid scramblase, Phospholipid scramblase 1,PL scramblase 1,PLSCR1,Tra1b,Tras1,MmTRA1b;Ca(2+)-dependent phospholipid scramblase 1;Erythrocyte phospholipid scramblase, Transplantability-associated protein 1,NOR1;TRA1, Phospholipid scramblase
Search name
Mouse PLSCR ELISA KIT ,Mouse MmTRA1b ELISA KIT ,Mouse Ca(2+)-dependent phospholipid scramblase 1 ELISA KIT ,Mouse Erythrocyte phospholipid scramblase ELISA KIT ,Mouse Phospholipid scramblase 1 ELISA KIT ,Mouse PL scramblase 1 ELISA KIT ,Mouse PLSCR1 ELISA KIT ,Mouse Tra1b ELISA KIT ,Mouse Tras1 ELISA KIT ,Mouse MmTRA1b ELISA KIT ,Mouse Ca(2+)-dependent phospholipid scramblase 1 ELISA KIT ,Mouse Erythrocyte phospholipid scramblase ELISA KIT ,Mouse Transplantability-associated protein 1 ELISA KIT ,Mouse NOR1 ELISA KIT ,Mouse TRA1 ELISA KIT ,Mouse Phospholipid scramblase ELISA KIT
Intended use
This immunoassay kit allows for the in vitro quantitative determination of Mouse phospholipid scramblase 1,PL scramblase 1 concentrations in serum, Plasma, tissue homogenates and Cell culture supernates and Other biological fluids.
Test principle
The microtiter plate provided in this kit has been pre-coated with an antibody specific to PL scramblase 1. Standards or samples are then added to the appropriate microtiter plate wells with a biotin-conjugated polyclonal antibody preparation specific for PL scramblase 1 and 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 PL scramblase 1, 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 PL scramblase 1 in the samples is then determined by comparing the O.D. of the samples to the standard curve.
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