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- 详细信息
- 文献和实验
- 技术资料
- 库存:
50
- 供应商:
LSMBIO
- 检测范围:
0.156-10ng/ml
- 检测方法:
夹心法/竞争法
- 应用:
夹心法/竞争法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 Nuclear nucleic acid-binding protein C1D,C1D
- 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:
0.078ng/ml
- 规格:
96T
Human Nuclear nucleic acid- binding protein C1D, C1D ELISA KIT
Product Name:Human Nuclear nucleic acid- binding protein C1D, C1D ELISA KIT
Packing:96T
Catalog No.:ELI-33295h
Gene Name:C1D
Detect Range:0.156-10 ng/mL
Sensitivity:0.078ng/mL
Target Protein Name:Nuclear nucleic acid-binding protein C1D(C1D
Alternative Name:C1D,Nuclear nucleic acid-binding protein C1D(C1D
Sample type:serum, plasma, tissue homogenates, cell culture supernates or other biological fluids.
ELISA type:Sandwich ELISA Kit
Product Description:Human Nuclear nucleic acid- binding protein C1D, C1D ELISA KIT allows for the in vitro quantitative determination of Nuclear nucleic acid-binding protein C1D(C1D concentrations in serum, plasma, tissue homogenates, cell culture supernates or other biological fluids.
ELISA Test Principle:
The microtiter plate provided in Human Nuclear nucleic acid- binding protein C1D, C1D ELISA KIT has been pre-coated with an Nuclear nucleic acid-binding protein C1D(C1D antibody specific to Nuclear nucleic acid-binding protein C1D(C1D .Standards or samples are then added to the appropriate microtiter plate wells with a biotin-conjugated antibody preparation specific for Nuclear nucleic acid-binding protein C1D(C1D 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 Nuclear nucleic acid-binding protein C1D(C1D, 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 Nuclear nucleic acid-binding protein C1D(C1D 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DNA-protein interactions are the basis for the molecular mechanisms responsible for nucleic-acid replication, gene transcription, recombination, viral integration, and gene regulation in both normal and pathophysiological conditions
Overview of Nucleic Acid Arrays
Abstract Table of Contents Figures Literature Cited Abstract Nucleic acid array technology refers
Nucleic Acid Programmable Protein Arrays: Versatile Tools for Array‐Based Functional Protein Studies
an alternate approach, the Nucleic Acid Programmable Protein Array (NAPPA) is constructed by spotting protein?encoding plasmid DNA at high density, in addressable fashion, on an array surface. Proteins are subsequently generated in situ
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