Extracellular matrix protein F
RAS1, Fras1 ELISA KIT/ Mouse Extracellular matrix protein FRAS1, Fras1 ELISA试剂盒- ￥2980
- LSM Bio
- 78-5000pg/ml
- 39pg/ml
- 进口
- ELI-07800m
- 2025年07月12日
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- 详细信息
- 文献和实验
- 技术资料
- 库存：
20
- 供应商：
LSM BIO
- 检测范围：
78-5000pg/ml
- 检测方法：
夹心法ELISA
- 应用：
检测小鼠血清，血浆，组织匀浆内的目标蛋白Extracellular matrix protein FRAS1, Fras1含量
- 适应物种：
小鼠
- 标记物：
Extracellular matrix protein FRAS1, Fras1
- 样本：
小鼠血清，血浆，组织匀浆及其他生物样本
- 灵敏度：
39pg/ml
- 规格：
96Tests
Mouse Extracellular matrix protein FRAS1, Fras1 ELISA KIT
Product Name:Mouse Extracellular matrix protein FRAS1, Fras1 ELISA KIT
Packing:96T
Catalog No.:ELI-07800m
Gene Name:Mouse Fras1
Detect Range:0.15-10ng/ml
Sensitivity:0.094ng/ml
Target Protein Name:Mouse Fras1
Alternative Name:Mouse Extracellular matrix protein FRAS1, Fras1
Sample type:serum, plasma, tissue homogenates, cell culture supernates or other biological fluids.
ELISA type:Sandwich ELISA Kit
Product Description:Mouse Extracellular matrix protein FRAS1, Fras1 ELISA KIT allows for the in vitro quantitative determination of Mouse Fras1 concentrations in serum, plasma, tissue homogenates, cell culture supernates or other biological fluids.
ELISA Test Principle:
The microtiter plate provided in Mouse Extracellular matrix protein FRAS1, Fras1 ELISA KIT has been pre-coated with an Mouse Extracellular matrix protein FRAS1, Fras1 antibody specific to Mouse Fras1 .Standards or samples are then added to the appropriate microtiter plate wells with a biotin-conjugated antibody preparation specific for Mouse Fras1 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 Mouse Fras1 , 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 Mouse Fras1 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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