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- 详细信息
- 文献和实验
- 技术资料
- 库存:
100
- 供应商:
LSM BIO
- 检测范围:
0.78-50ng/ml
- 检测方法:
夹心法
- 应用:
利用ELISA方法体外定量检测牛血清,血浆等样本中目标蛋白的浓度
- 适应物种:
牛
- 标记物:
Bovine Zinc transporter ZIP11,SLC39A11
- 样本:
牛的血浆,血清,细胞上清等
- 灵敏度:
0.469ng/ml
- 规格:
96tests
Bovine Zinc transporter ZIP11, SLC39A11 ELISA KIT
Product Name:Bovine Zinc transporter ZIP11, SLC39A11 ELISA KIT
Packing:96T
Catalog No.:ELI-53097b
Gene Name:Bovine Zinc transporter ZIP11, SLC39A11
Detect Range:31.2-2000pg/ml
Sensitivity:18.75pg/ml
Target Protein Name:Bovine Zinc transporter ZIP11, SLC39A11
Alternative Name:SLC39A11,Bovine Zinc transporter ZIP11, SLC39A11
Sample type:serum, plasma, tissue homogenates, cell culture supernates or other biological fluids.
ELISA type:Sandwich ELISA Kit
Product Description:Bovine Zinc transporter ZIP11, SLC39A11 ELISA KIT allows for the in vitro quantitative determination of Bovine Zinc transporter ZIP11, SLC39A11 concentrations in serum, plasma, tissue homogenates, cell culture supernates or other biological fluids.
ELISA Test Principle:
The microtiter plate provided in Bovine Zinc transporter ZIP11, SLC39A11 ELISA KIT has been pre-coated with an Bovine Zinc transporter ZIP11, SLC39A11 antibody specific to Bovine Zinc transporter ZIP11, SLC39A11 .Standards or samples are then added to the appropriate microtiter plate wells with a biotin-conjugated antibody preparation specific for Bovine Zinc transporter ZIP11, SLC39A11 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 Zinc transporter ZIP11, SLC39A11, 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 Zinc transporter ZIP11, SLC39A11 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Gene Editing in One‐Cell Embryos by Zinc‐Finger and TAL Nucleases
Wiley & Sons, Inc. Keywords: pronucleus injection; gene targeting; mouse mutant; zinc?finger nuclease; TAL nuclease; homologous recombination
to make contact with bases in the target DNA subsite11-15 . Figure 1: In vivo screening system and zinc 'fingerprints'. (A) Zinc-finger screening system in yeast. Zinc-finger domain 'A' recognizes the 3-bp target DNA subsite (designated XXX
that tissuesfrom GSK-3b-deficient mice do not show accumulation of b-catenin(11) . In GSK-3b-deficient mouse cells, GSK-3a was also foundprecipitated with axin (11) . These data indicate that GSK-3aand GSK-3b can substitute for each other in the regulation ofb
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