Cerebellar degeneration-relate
d protein 2, Cdr2 ELISA KIT/ Mouse Cerebellar degeneration-related protein 2, Cdr2 ELISA试剂盒- ￥2980
- LSM Bio
- 78-5000pg/ml
- 39pg/ml
- 进口
- ELI-24840m
- 2025年07月11日
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- 详细信息
- 文献和实验
- 技术资料
- 库存：
50
- 供应商：
LSM BIO
- 检测范围：
78-5000pg/ml
- 检测方法：
夹心法ELISA或竞争法ELISA
- 应用：
检测小鼠血清，血浆，组织匀浆内的目标蛋白含量
- 适应物种：
小鼠
- 标记物：
Cerebellar degeneration-related protein 2, Cdr2
- 样本：
小鼠血清，血浆，组织匀浆
- 灵敏度：
39pg/ml
- 规格：
96Tests
Mouse Cerebellar degeneration- related protein 2, Cdr2 ELISA KIT
Product Name:Mouse Cerebellar degeneration- related protein 2, Cdr2 ELISA KIT
Packing:96T
Catalog No.:ELI-24840m
Gene Name:Mouse Cdr2
Detect Range:15.62-1000pg/ml
Sensitivity:9.375pg/ml
Target Protein Name:Mouse Cdr2
Alternative Name:Mouse Cerebellar degeneration-related protein 2, Cdr2
Sample type:serum, plasma, tissue homogenates, cell culture supernates or other biological fluids.
ELISA type:Sandwich ELISA Kit
Product Description:Mouse Cerebellar degeneration- related protein 2, Cdr2 ELISA KIT allows for the in vitro quantitative determination of Mouse Cdr2 concentrations in serum, plasma, tissue homogenates, cell culture supernates or other biological fluids.
ELISA Test Principle:
The microtiter plate provided in Mouse Cerebellar degeneration- related protein 2, Cdr2 ELISA KIT has been pre-coated with an Mouse Cerebellar degeneration-related protein 2, Cdr2 antibody specific to Mouse Cdr2 .Standards or samples are then added to the appropriate microtiter plate wells with a biotin-conjugated antibody preparation specific for Mouse Cdr2 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 Mouse Cdr2 , 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 Mouse Cdr2 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Discovery Genetics: The History and Future of Spontaneous Mutation Research
.S., Heckenlively, J.R., and Swaroop, A. 2006. In‐frame deletion in a novel centrosomal/ciliary protein CEP290/NPHP6 perturbs its interaction with RPGR and results in early‐onset retinal degeneration in the rd16 mouse. Hum. Mol. Genet. 15:1847‐1857
, axin, and the tumor suppressor, adenomatouspolyposis coli (APC) protein (3) . In the absence of Wnt signaling,GSK-3 targets b-catenin for ubiquitin-mediated proteosomaldegradation by phosphorylation of b-catenin, axin, and APC (3) . Phosphorylation
Analysis of Oxidative Modification of Proteins
Support Protocol 4: Analysis of Protein‐Bound Notrotyrosine by a Competitive ELISA Method Basic Protocol 5: Enzymatic Analysis of Isoaspartate Formation Support Protocol 5: Gel Electrophoretic
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