- ￥2890
- LSM Bio
- 0.31-20ng/Ml
- 0.1ng/Ml
- 进口
- ELI-44362h
- 2025年07月16日
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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：
0.31-20ng/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 Double-stranded RNA-specific editase 1,ADARB1
- 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：
0.1ng/Ml
- 规格：
96T
Human Double-stranded RNA-specific editase 1,ADARB1 ELISA KIT
Product Name:Human Double-stranded RNA-specific editase 1,ADARB1 ELISA KIT
Packing:96T
Catalog No.:Human ADARB1 ELISA KIT
Gene Name:ADARB1
Detect Range:0.312-20 ng/mL
Sensitivity:0.039ng/mL
Target Protein Name:Human ADARB1
Alternative Name:Human ADARB1
Sample type:serum, plasma, tissue homogenates, cell culture supernates or other biological fluids.
ELISA type:Sandwich ELISA Kit
Product Description:Human ADARB1 ELISA KIT allows for the in vitro quantitative determination of Human ADARB1 concentrations in serum, plasma, tissue homogenates, cell culture supernates or other biological fluids.
ELISA Test Principle:
The microtiter plate provided in Human ADARB1 ELISA KIT has been pre-coated with an Human ADARB1 antibody specific to Human ADARB1 .Standards or samples are then added to the appropriate microtiter plate wells with a biotin-conjugated antibody preparation specific for Human ADARB1 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 ADARB1, 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 ADARB1 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RNA Analysis by Nuclease Protection
extension from double‐stranded PCR products. A specific nested primer oligonucleotide designed to hybridize to a specific sequence on the PCR product is added, then the resulting ssDNA probe is generated and purified as described
) Short double-stranded RNA induces transcriptional gene silencing in human cancer cells in the absence of DNA methylation, Nature Genetics, 37(8): 906-910. 6.Weinberg, M.S., Villeneuve, L.M., Ehsani, A., Amarzguioui, M., Aagaard, L., Chen, Z., Riggs
RNA‐Seq: A Method for Comprehensive Transcriptome Analysis
Basic Protocol 1: cDNA Library Preparation Using Fragmented Double‐Stranded cDNA Alternate Protocol 1: cDNA Library Preparation Using Hydrolyzed or Fragmented RNA Support Protocol 1: Purification
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