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MOCS1 (基因名), Molybdenum cofactor biosynthesis protein 1 (蛋白名), MOCS1_HUMAN.
产品名称:

Human MOCS1/ Molybdenum cofactor biosynthesis protein 1 Recombinant Protein

货号:

R9765h

商标:
EIAab®
监管等级:
别名:

Cell migration-inducing gene 11 protein, Molybdenum cofactor synthesis-step 1 protein A-B, MIG11

序列号:
Q9NZB8
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 MOCS1 Protein
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Human MOCS1 Protein
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产品说明书
说明书: 下载说明书
MSDS: MSDS


R&D 技术数据
更多信息,请参阅手册,或联系我们的技术支持: tech@eiaab.com.
基因位点
Cytogenetic band: 6p21.2 by HGNC 6p21.2 by Entrez Gene 6p21.2 by Ensembl
MOCS1 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:
Isoform MOCS1A and isoform MOCS1B probably form a heterooligomer.


功能:
Isoform MOCS1A and isoform MOCS1B probably form a complex that catalyzes the conversion of 5'-GTP to cyclic pyranopterin monophosphate (cPMP). MOCS1A catalyzes the cyclization of GTP to (8S)-3',8-cyclo-7,8-dihydroguanosine 5'-triphosphate and MOCS1B catalyzes the subsequent conversion of (8S)-3',8-cyclo-7,8-dihydroguanosine 5'-triphosphate to cPMP.


亚细胞位置:
N/A


该产品尚未在任何出版物中被引用。

[1].
"Mutations in a polycistronic nuclear gene associated with molybdenum cofactor deficiency."

[2].
"Ten novel mutations in the molybdenum cofactor genes MOCS1 and MOCS2 and in vitro characterization of a MOCS2 mutation that abolishes the binding ability of molybdopterin synthase."

[3].
"Characterization of MOCS1A, an oxygen-sensitive iron-sulfur protein involved in human molybdenum cofactor biosynthesis."

[4].
"Mutations in the molybdenum cofactor biosynthetic genes MOCS1, MOCS2, and GEPH."

[5].
"Functionality of alternative splice forms of the first enzymes involved in human molybdenum cofactor biosynthesis."

[6].
"The bicistronic MOCS1 gene has alternative start codons on two mutually exclusive exons."

[7].
"Diverse splicing mechanisms fuse the evolutionarily conserved bicistronic MOCS1A and MOCS1B open reading frames."

[8].
"Human molybdopterin synthase gene: genomic structure and mutations in molybdenum cofactor deficiency type B."

[9].
"Genomic structure and mutational spectrum of the bicistronic MOCS1 gene defective in molybdenum cofactor deficiency type A."

[10].
"An unusual genetic variant in the MOCS1 gene leads to complete missplicing of an alternatively spliced exon in a patient with molybdenum cofactor deficiency."
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