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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:
Meckel syndrome type 1 protein homolog, Mks1
- 样本:
小鼠血清,血浆,组织匀浆
- 灵敏度:
39pg/ml
- 规格:
96Tests
Mouse Meckel syndrome type 1 protein homolog, Mks1 ELISA KIT
Product Name:Mouse Meckel syndrome type 1 protein homolog, Mks1 ELISA KIT
Packing:96T
Catalog No.:ELI-16533m
Gene Name:Mouse Mks1
Detect Range:78.1-5000pg/ml
Sensitivity:46.9pg/ml
Target Protein Name:Mouse Mks1
Alternative Name:Mouse Meckel syndrome type 1 protein homolog, Mks1
Sample type:serum, plasma, tissue homogenates, cell culture supernates or other biological fluids.
ELISA type:Sandwich ELISA Kit
Product Description:Mouse Meckel syndrome type 1 protein homolog, Mks1 ELISA KIT allows for the in vitro quantitative determination of Mouse Mks1 concentrations in serum, plasma, tissue homogenates, cell culture supernates or other biological fluids.
ELISA Test Principle:
The microtiter plate provided in Mouse Meckel syndrome type 1 protein homolog, Mks1 ELISA KIT has been pre-coated with an Mouse Meckel syndrome type 1 protein homolog, Mks1 antibody specific to Mouse Mks1 .Standards or samples are then added to the appropriate microtiter plate wells with a biotin-conjugated antibody preparation specific for Mouse Mks1 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 Mks1 , 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 Mks1 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[资源] 所有的看家基因(housekeeping genes)列表+引物设计服务
reticulon 4 (RTN4), mRNA 1267 NM_006782 Homo sapiens zinc finger protein-like 1 (ZFPL1), mRNA 712 NM_006694 Homo sapiens jumping translocation breakpoint (JTB ), mRNA 2394 NM_006703 Homo sapiens nudix (nucleoside diphosphate linked moiety X)-type
a subset of genomic DNA sequences of type 5'-(NNN )3 -3', whereas the 6ZF library would recognize a subset of genomic sequences of type 5'-(NNN )6 -3'. Given the zinc-finger domains used, both libraries were more likely to recognize (RNN)x -type sequences
Discovery Genetics: The History and Future of Spontaneous Mutation Research
of synpolydactyly. Genetics 183:23‐30. Cook, S.A., Collin, G.B., Bronson, R.T., Naggert, J.K., Liu, D.P., Akeson, E.C., and Davisson, M.T. 2009. A mouse model for Meckel syndrome type
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