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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:
0.15-10ng/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:
Gamma- interferon- inducible protein 16, IFI16
- 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 Gamma- interferon- inducible protein 16, IFI16 ELISA KIT
Product Name:Human Gamma- interferon- inducible protein 16, IFI16 ELISA KIT
Packing:96T
Catalog No.:ELI-06103h
Gene Name:IFI16
Detect Range:0.156-10 ng/mL
Sensitivity:0.078ng/mL
Target Protein Name:Gamma-interferon-inducible protein 16(IFI16
Alternative Name:IFI16,Gamma-interferon-inducible protein 16(IFI16
Sample type:serum, plasma, tissue homogenates, cell culture supernates or other biological fluids.
ELISA type:Sandwich ELISA Kit
Product Description:Human Gamma- interferon- inducible protein 16, IFI16 ELISA KIT allows for the in vitro quantitative determination of Gamma-interferon-inducible protein 16(IFI16 concentrations in serum, plasma, tissue homogenates, cell culture supernates or other biological fluids.
ELISA Test Principle:
The microtiter plate provided in Human Gamma- interferon- inducible protein 16, IFI16 ELISA KIT has been pre-coated with an Gamma-interferon-inducible protein 16(IFI16 antibody specific to Gamma-interferon-inducible protein 16(IFI16 .Standards or samples are then added to the appropriate microtiter plate wells with a biotin-conjugated antibody preparation specific for Gamma-interferon-inducible protein 16(IFI16 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 Gamma-interferon-inducible protein 16(IFI16, 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 Gamma-interferon-inducible protein 16(IFI16 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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