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MSH5 (基因名), MutS protein homolog 5 (蛋白名), MSH5_HUMAN.
产品名称:

Human MSH5/ MutS protein homolog 5 Recombinant Protein

货号:
-
商标:
EIAab®
监管等级:
别名:

hMSH5

序列号:
O43196
来源:
E.coli
种属:
Human
标签:
His
纯度:
>90% by SDS-PAGE
浓度:
Reconstitution Dependent
形态:
Liquid
内毒素水平:
Please contact protein@eiaab.com The technician for more information.
应用:
存储缓冲液:
50mM NaH2PO4, 500mM NaCl Buffer with 500mM Imidazole, 10%glycerol(PH8.0)
存储:
Store at -20°C. (Avoid repeated freezing and thawing.)
研究领域:
-
Human MSH5 Protein
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Human MSH5 Protein
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产品说明书
说明书: 下载说明书
MSDS: MSDS


基因位点
Cytogenetic band: 6p21.33 by HGNC 6p21.33 by Entrez Gene 6p21.33 by Ensembl
MSH5 Gene in genomic location: bands according to Ensembl, locations according to GeneLoc (and/or Entrez Gene and/or Ensembl if different)
基因位点
通用注释


亚单元:
Heterooligomer of MSH4 and MSH5. Interacts with HJURP.


功能:
Involved in meiotic recombination. Facilitate crossovers between homologs during meiosis.


亚细胞位置:
N/A


该产品尚未在任何出版物中被引用。

[1].
"Cloning, structural characterization, and chromosomal localization of the human orthologue of Saccharomyces cerevisiae MSH5 gene."

[2].
"Cloning and characterization of the human and Caenorhabditis elegans homologs of the Saccharomyces cerevisiae MSH5 gene."

[3].
"Genetic investigation of four meiotic genes in women with premature ovarian failure."

[4].
"Mutations in MSH5 in primary ovarian insufficiency."

[5].
"The role of MSH5 C85T and MLH3 C2531T polymorphisms in the risk of male infertility with azoospermia or severe oligozoospermia."

[6].
"Evaluation of 172 candidate polymorphisms for association with oligozoospermia or azoospermia in a large cohort of men of European descent."

[7].
"MSH5 is not a genetic predisposing factor for immunoglobulin A deficiency but marks the HLA-DRB1*0102 subgroup carrying susceptibility."

[8].
"Examination of genetic polymorphisms in newborns for signatures of sex-specific prenatal selection."

[9].
"Genetically determined Amerindian ancestry correlates with increased frequency of risk alleles for systemic lupus erythematosus."

[10].
"Several loci in the HLA class III region are associated with T1D risk after adjusting for DRB1-DQB1."
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