Far upstream element-binding p
rotein 2, Khsrp ELISA KIT/ Mouse Far upstream element-binding protein 2, Khsrp ELISA试剂盒- ￥2980
- LSM Bio
- 78-5000pg/ml
- 39pg/ml
- 进口
- ELI-27582m
- 2025年07月15日
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- 详细信息
- 文献和实验
- 技术资料
- 库存：
50
- 供应商：
LSM BIO
- 检测范围：
78-5000pg/ml
- 检测方法：
夹心法ELISA或竞争法ELISA
- 应用：
检测小鼠血清，血浆，组织匀浆内的目标蛋白含量
- 适应物种：
小鼠
- 标记物：
Far upstream element-binding protein 2, Khsrp
- 样本：
小鼠血清，血浆，组织匀浆
- 灵敏度：
39pg/ml
- 规格：
96Tests
Mouse Far upstream element- binding protein 2, Khsrp ELISA KIT
Product Name:Mouse Far upstream element- binding protein 2, Khsrp ELISA KIT
Packing:96T
Catalog No.:ELI-27582m
Gene Name:Mouse Khsrp
Detect Range:78-5000pg/ml
Sensitivity:46.9pg/ml
Target Protein Name:Mouse Khsrp
Alternative Name:Mouse Far upstream element-binding protein 2, Khsrp
Sample type:serum, plasma, tissue homogenates, cell culture supernates or other biological fluids.
ELISA type:Sandwich ELISA Kit
Product Description:Mouse Far upstream element- binding protein 2, Khsrp ELISA KIT allows for the in vitro quantitative determination of Mouse Khsrp concentrations in serum, plasma, tissue homogenates, cell culture supernates or other biological fluids.
ELISA Test Principle:
The microtiter plate provided in Mouse Far upstream element- binding protein 2, Khsrp ELISA KIT has been pre-coated with an Mouse Far upstream element-binding protein 2, Khsrp antibody specific to Mouse Khsrp .Standards or samples are then added to the appropriate microtiter plate wells with a biotin-conjugated antibody preparation specific for Mouse Khsrp 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 Khsrp , 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 Khsrp 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fi eld. In the past decades, genome editing tools based onsequence-specifi c nucleases and DNA-binding proteins such aszinc-fi nger nucleases (ZFNs) [ 1 – 4 ], meganucleases [ 5 ], and transcriptionactivator like effectors (TALEs) [ 6 – 11
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
of distance for the distance. i mean we should only consider a certain distance upstream, like within 1kb. am i right?how about those binding sites downstream of the TSP primers? doesn't matter?how long fragment can you get using this kit? can we use long PCR
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