库存 ：货源充足

供应商 ：LSM Bio

检测限 ：详见说明书

检测方法 ： 夹心法/竞争法

应用 ：夹心法/竞争法ELISA体外定量检测小鼠血清、血浆或其它相关生物液体中蛋白浓度

适应物种 ：牛

标记物 ：详见说明书

样本 ：血清、血浆或其它相关生物液体中天然和重组蛋白

规格 ：96T

Bovine DNA repair protein RAD51 homolog 4, RAD51D ELISA KIT

Product Name:Bovine DNA repair protein RAD51 homolog 4, RAD51D ELISA KIT
Packing:96T

Catalog No.:ELI-19597b

Gene Name:Bovine DNA repair protein RAD51 homolog 4, RAD51D

Detect Range:15.625-1000pg/ml

Sensitivity:9.375pg/ml

Target Protein Name:Bovine DNA repair protein RAD51 homolog 4, RAD51D

Alternative Name:RAD51D,Bovine DNA repair protein RAD51 homolog 4, RAD51D
Sample type:serum, plasma, tissue homogenates, cell culture supernates or other biological fluids.

ELISA type:Sandwich ELISA Kit
Product Description:Bovine DNA repair protein RAD51 homolog 4, RAD51D ELISA KIT allows for the in vitro quantitative determination of Bovine DNA repair protein RAD51 homolog 4, RAD51D concentrations in serum, plasma, tissue homogenates, cell culture supernates or other biological fluids.

ELISA Test Principle:
The microtiter plate provided in Bovine DNA repair protein RAD51 homolog 4, RAD51D ELISA KIT has been pre-coated with an Bovine DNA repair protein RAD51 homolog 4, RAD51D antibody specific to Bovine DNA repair protein RAD51 homolog 4, RAD51D .Standards or samples are then added to the appropriate microtiter plate wells with a biotin-conjugated antibody preparation specific for Bovine DNA repair protein RAD51 homolog 4, RAD51D 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 Bovine DNA repair protein RAD51 homolog 4, RAD51D, 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.The concentration of Bovine DNA repair protein RAD51 homolog 4, RAD51D in the samples is then determined by comparing the O.D. of the samples to the standard curve.

NOTE:FOR RESEARCH USE ONLY; NOT FOR THERAPEUTIC OR DIAGNOSTIC APPLICATIONS! PLEASE READ ENTIRE PROCEDURE!

 

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