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- 详细信息
- 文献和实验
- 技术资料
- 库存:
20
- 供应商:
LSMBIO
- 检测范围:
0.156-10ng/ML
- 检测方法:
夹心法
- 应用:
夹心法ELISA体外定量检测人血清、血浆或其它相关生物液体中蛋白浓度
- 适应物种:
人
- 标记物:
Human Putative zinc finger protein 818,ZNF818P
- 样本:
人血清、血浆或其它相关生物液体中天然和重组蛋白
- 灵敏度:
0.078 ng/Ml
- 规格:
96T
Human Putative zinc finger protein 818,ZNF818P ELISA KIT
Product Name:Human Putative zinc finger protein 818,ZNF818P ELISA KIT
Packing:96T
Catalog No.:Human ZNF818P ELISA KIT
Gene Name:ZNF818P
Detect Range:0.312-20 ng/mL
Sensitivity:0.039ng/mL
Target Protein Name:Human ZNF818P
Alternative Name:Human ZNF818P
Sample type:serum, plasma, tissue homogenates, cell culture supernates or other biological fluids.
ELISA type:Sandwich ELISA Kit
Product Description:Human ZNF818P ELISA KIT allows for the in vitro quantitative determination of Human ZNF818P concentrations in serum, plasma, tissue homogenates, cell culture supernates or other biological fluids.
ELISA Test Principle:
The microtiter plate provided in Human ZNF818P ELISA KIT has been pre-coated with an Human ZNF818P antibody specific to Human ZNF818P .Standards or samples are then added to the appropriate microtiter plate wells with a biotin-conjugated antibody preparation specific for Human ZNF818P 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 Human ZNF818P, 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 Human ZNF818P 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
via embryo microinjection of zinc‐finger nucleases. Science 325:433. Hasty, P., Abuin, A., and Bradley, A. 2000. Gene targeting, principles, and practice in mammalian cells
Overview of Protein Microarrays
. Protocols 1:755‐768. Charboneau, L., Tory, H., Chen, T., Winters, M., Petricoin, E.F. III, Liotta, L.A., and Paweletz, C.P. 2002. Utility of reverse phase protein arrays
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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