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AHCY (基因名), Adenosylhomocysteinase (蛋白名), sahh_human.
产品名称:

Human AHCY/ Adenosylhomocysteinase Recombinant Protein
腺苷高半胱

货号:

R12634h

商标:
EIAab®
监管等级:
别名:

S-adenosyl-L-homocysteine hydrolase, AdoHcyase, SAHH

序列号:
P23526
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:
Cell Biology
Human AHCY Protein
规格 & 价格: cart
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Human AHCY Protein
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产品说明书
说明书: 下载说明书
MSDS: MSDS
在线询价


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: 20q11.22 by HGNC 20q11.22 by Entrez Gene 20q11.22 by Ensembl
AHCY 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.


功能:
Adenosylhomocysteine is a competitive inhibitor of S-adenosyl-L-methionine-dependent methyl transferase reactions; therefore adenosylhomocysteinase may play a key role in the control of methylations via regulation of the intracellular concentration of adenosylhomocysteine.


亚细胞位置:
Cytoplasm Melanosome Identified by mass spectrometry in melanosome fractions from stage I to stage IV.


该产品尚未在任何出版物中被引用。

[1].
"Effect of genetic variation in the human S-adenosylhomocysteine hydrolase gene on total homocysteine concentrations and risk of recurrent venous thrombosis."

[2].
"S-adenosylhomocysteine hydrolase deficiency in a human: a genetic disorder of methionine metabolism."

[3].
"Catalytic strategy of S-adenosyl-L-homocysteine hydrolase: transition-state stabilization and the avoidance of abortive reactions."

[4].
"Limited proteolysis of S-adenosylhomocysteine hydrolase: implications for the three-dimensional structure."

[5].
"Contribution of adenosine related genes to the risk of depression with disturbed sleep."

[6].
"Early-onset ischaemic stroke: analysis of 58 polymorphisms in 17 genes involved in methionine metabolism."

[7].
"A candidate gene study of folate-associated one carbon metabolism genes and colorectal cancer risk."

[8].
"Variation at the NFATC2 locus increases the risk of thiazolidinedione-induced edema in the Diabetes REduction Assessment with ramipril and rosiglitazone Medication (DREAM) study."

[9].
"Maternal genes and facial clefts in offspring: a comprehensive search for genetic associations in two population-based cleft studies from Scandinavia."

[10].
"Oral facial clefts and gene polymorphisms in metabolism of folate/one-carbon and vitamin A: a pathway-wide association study."
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