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MOCOS (基因名), Molybdenum cofactor sulfurase (蛋白名), MOCOS_HUMAN.
产品名称:

Human MOCOS/ Molybdenum cofactor sulfurase Recombinant Protein
铁钼辅因子硫化

货号:

R13459h

商标:
EIAab®
监管等级:
别名:

Molybdenum cofactor sulfurtransferase, MCS

序列号:
Q96EN8
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:
Metabolism
Human MOCOS Protein
规格 & 价格: cart
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Human MOCOS 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: 18q12.2 by HGNC 18q12.2 by Entrez Gene 18q12.2 by Ensembl
MOCOS 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:
N/A


功能:
Sulfurates the molybdenum cofactor. Sulfation of molybdenum is essential for xanthine dehydrogenase (XDH) and aldehyde oxidase (ADO) enzymes in which molybdenum cofactor is liganded by 1 oxygen and 1 sulfur atom in active form. In vitro, the C-terminal domain is able to reduce N-hydroxylated prodrugs, such as benzamidoxime.


亚细胞位置:
N/A


该产品尚未在任何出版物中被引用。

[1].
"Mutation of human molybdenum cofactor sulfurase gene is responsible for classical xanthinuria type II."

[2].
"Novel pharmacogenetic markers for treatment outcome in azathioprine-treated inflammatory bowel disease."

[3].
"Identification and characterization of the first mutation (Arg776Cys) in the C-terminal domain of the Human Molybdenum Cofactor Sulfurase (HMCS) associated with type II classical xanthinuria."

[4].
"A probability-based approach for high-throughput protein phosphorylation analysis and site localization."

[5].
"Identification of the missing component in the mitochondrial benzamidoxime prodrug-converting system as a novel molybdenum enzyme."

[6].
"The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC)."

[7].
"Identification of a new point mutation in the human molybdenum cofactor sulferase gene that is responsible for xanthinuria type II."

[8].
"Architecture of the human interactome defines protein communities and disease networks."

[9].
"Genome-wide CRISPR screen identifies HNRNPL as a prostate cancer dependency regulating RNA splicing."

[10].
"The BioPlex Network: A Systematic Exploration of the Human Interactome."
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