Human Filamin- A, FLNA ELISA KIT
96 Tests
Operating instruction
FOR RESEARCH USE ONLY; NOT FOR THERAPEUTIC OR DIAGNOSTIC APPLICATIONS!PLEASE READ THROUGH ENTIRE PROCEDURE BEFORE BEGINNING!
Synonyms
FLNA,FLN-A; ABP-280; ABPX; CSBS; CVD1; FLN; FLN1; FMD; MNS; NHBP; OPD; OPD1; OPD2; XLVD; XMVD; actin binding protein 280; alpha-filamin; endothelial actin-binding protein; filamin-1; filamin-A; non-muscle filamin; filamin A alpha, Filamin-A
Search name
Human FLNA ELISA KIT ,Human FLN-A ELISA KIT ,Human ABP-280 ELISA KIT ,Human ABPX ELISA KIT ,Human CSBS ELISA KIT ,Human CVD1 ELISA KIT ,Human FLN ELISA KIT ,Human FLN1 ELISA KIT ,Human FMD ELISA KIT ,Human MNS ELISA KIT ,Human NHBP ELISA KIT ,Human OPD ELISA KIT ,Human OPD1 ELISA KIT ,Human OPD2 ELISA KIT ,Human XLVD ELISA KIT ,Human XMVD ELISA KIT ,Human actin binding protein 280 ELISA KIT ,Human alpha-filamin ELISA KIT ,Human endothelial actin-binding protein ELISA KIT ,Human filamin-1 ELISA KIT ,Human filamin-A ELISA KIT ,Human non-muscle filamin ELISA KIT ,Human filamin A alpha ELISA KIT ,Human Filamin-A ELISA KIT
Intended use
This immunoassay kit allows for the in vitro quantitative determination of human filamin-a,FLN-A 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 FLN-A. Standards or samples are then added to the appropriate microtiter plate wells with a biotin-conjugated polyclonal antibody preparation specific for FLN-A 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 FLN-A, 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 FLN-A in the samples is then determined by comparing the O.D. of the samples to the standard curve.
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