EIAab
首页  >  重组蛋白  >  Human MAT1A Recombinant Protein
MAT1A (基因名), S-adenosylmethionine synthase isoform type-1 (蛋白名), METK1_HUMAN.
产品名称:

Human MAT1A/ S-adenosylmethionine synthase isoform type-1 Recombinant Protein
蛋氨酸腺苷转移酶1

货号:

R0246h

商标:
EIAab®
监管等级:
别名:

Methionine adenosyltransferase 1, Methionine adenosyltransferase I/III, MAT 1, MAT-I/III, AdoMet synthase 1, AMS1, MATA1

序列号:
Q00266
来源:
E.coli
种属:
Human
标签:
His
序列:
1-395aa
预估分子量:
43.45 kDa (monomer)
纯度:
Greater than 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 MAT1A Protein
规格 & 价格: cart
×
Human MAT1A Protein
邮箱 *
消息 *
Please 登录.
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: 10q22.3 by HGNC 10q22.3 by Entrez Gene 10q22.3 by Ensembl
MAT1A 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:
Homotetramer (MAT-I); dimer of dimers (PubMed:23425511). Homodimer (MAT-III).


功能:
Catalyzes the formation of S-adenosylmethionine from methionine and ATP. The reaction comprises two steps that are both catalyzed by the same enzyme: formation of S-adenosylmethionine (AdoMet) and triphosphate, and subsequent hydrolysis of the triphosphate.


亚细胞位置:
N/A


该产品尚未在任何出版物中被引用。

[1].
"Demyelination of the brain is associated with methionine adenosyltransferase I/III deficiency."

[2].
"MAT1A variants are associated with hypertension, stroke, and markers of DNA damage and are modulated by plasma vitamin B-6 and folate."

[3].
"Methionine adenosyltransferase I/III deficiency: novel mutations and clinical variations."

[4].
"Dominant inheritance of isolated hypermethioninemia is associated with a mutation in the human methionine adenosyltransferase 1A gene."

[5].
"Molecular mechanisms of an inborn error of methionine pathway. Methionine adenosyltransferase deficiency."

[6].
"Characterization of a full-length cDNA encoding human liver S-adenosylmethionine synthetase: tissue-specific gene expression and mRNA levels in hepatopathies."

[7].
"Insight into S-adenosylmethionine biosynthesis from the crystal structures of the human methionine adenosyltransferase catalytic and regulatory subunits."

[8].
"Human variation in alcohol response is influenced by variation in neuronal signaling genes."

[9].
"Variation at the NFATC2 locus increases the risk of thiazolidinedione-induced edema in the Diabetes REduction Assessment with ramipril and rosiglitazone Medication (DREAM) study."

[10].
"Maternal genes and facial clefts in offspring: a comprehensive search for genetic associations in two population-based cleft studies from Scandinavia."
关闭
Sample Data
关闭
Sample Data
关闭
Sample Data
用户中心 close
购物车 close
我的收藏 close
我的足迹 close
清除
产品对比 close
用户中心
购物车
我的收藏
我的足迹
产品对比
回到顶部
消息
close_message
产品名称 *
邮箱 *
消息 *
通知
new 留 言
规格 数量 单价 (¥) 小计 1 (¥)
小计 2:
triangle
规格 数量 单价 (¥)
你想做我们的代理并得到更低的折扣吗?
请联系我们:
电话:027-59234612(+86)
传真:027-59234610(+86)
邮箱:sales@eiaab.com