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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Uncharacterized protein C11orf74 homolog, Nwc含量
- 适应物种:
小鼠
- 标记物:
Uncharacterized protein C11orf74 homolog, Nwc
- 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 Uncharacterized protein C11orf74 homolog, Nwc ELISA KIT
Product Name:Mouse Uncharacterized protein C11orf74 homolog, Nwc ELISA KIT
Packing:96T
Catalog No.:ELI-10986m
Gene Name:Mouse Nwc
Detect Range:0.15-10ng/ml
Sensitivity:0.094ng/ml
Target Protein Name:Mouse Nwc
Alternative Name:Mouse Uncharacterized protein C11orf74 homolog, Nwc
Sample type:serum, plasma, tissue homogenates, cell culture supernates or other biological fluids.
ELISA type:Sandwich ELISA Kit
Product Description:Mouse Uncharacterized protein C11orf74 homolog, Nwc ELISA KIT allows for the in vitro quantitative determination of Mouse Nwc concentrations in serum, plasma, tissue homogenates, cell culture supernates or other biological fluids.
ELISA Test Principle:
The microtiter plate provided in Mouse Uncharacterized protein C11orf74 homolog, Nwc ELISA KIT has been pre-coated with an Mouse Uncharacterized protein C11orf74 homolog, Nwc antibody specific to Mouse Nwc .Standards or samples are then added to the appropriate microtiter plate wells with a biotin-conjugated antibody preparation specific for Mouse Nwc 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 Nwc , 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 Nwc 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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文献和实验specificity of each fusion protein was tested by ELISA using a panel of DNA substrates (Fig. 2B,C). The predicted DNA binding site of each TFZF was decoded from the -helical sequence of the corresponding zinc finger (Table 1). As expected, the majority
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