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BAAT (基因名), Bile acid-CoA:amino acid N-acyltransferase (蛋白名), baat_human.
产品名称:

Human BAAT/ Bile acid-CoA:amino acid N-acyltransferase Recombinant Protein

货号:

R15771h

商标:
EIAab®
监管等级:
别名:

Glycine N-choloyltransferase, Long-chain fatty-acyl-CoA hydrolase, BACAT

序列号:
Q14032
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:
Cardiovascular
Human BAAT Protein
规格 & 价格: cart
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Human BAAT Protein
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产品说明书
说明书: 下载说明书
MSDS: MSDS
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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: 9q31.1 by HGNC 9q31.1 by Entrez Gene 9q31.1 by Ensembl
BAAT 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:
Monomer.


功能:
Involved in bile acid metabolism. In liver hepatocytes catalyzes the second step in the conjugation of C24 bile acids (choloneates) to glycine and taurine before excretion into bile canaliculi. The major components of bile are cholic acid and chenodeoxycholic acid. In a first step the bile acids are converted to an acyl-CoA thioester, either in peroxisomes (primary bile acids deriving from the cholesterol pathway), or cytoplasmic at the endoplasmic reticulum (secondary bile acids). May catalyze the conjugation of primary or secondary bile acids, or both. The conjugation increases the detergent properties of bile acids in the intestine, which facilitates lipid and fat-soluble vitamin absorption. In turn, bile acids are deconjugated by bacteria in the intestine and are recycled back to the liver for reconjugation (secondary bile acids). May also act as an acyl-CoA thioesterase that regulates intracellular levels of free fatty acids. In vitro, catalyzes the hydrolysis of long- and very long-chain saturated acyl-CoAs to the free fatty acid and coenzyme A (CoASH), and conjugates glycine to these acyl-CoAs.


亚细胞位置:
Cytoplasm


该产品尚未在任何出版物中被引用。

[1].
"Human and rat bile acid-CoA:amino acid N-acyltransferase are liver-specific peroxisomal enzymes: implications for intracellular bile salt transport."

[2].
"Genetic polymorphism of bile acid CoA: amino acid N-acyltransferase in Japanese individuals."

[3].
"Complex inheritance of familial hypercholanemia with associated mutations in TJP2 and BAAT."

[4].
"The human bile acid-CoA:amino acid N-acyltransferase functions in the conjugation of fatty acids to glycine."

[5].
"An approach based on a genome-wide association study reveals candidate loci for narcolepsy."

[6].
"DNA sequence and analysis of human chromosome 9."

[7].
"The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC)."

[8].
"Conserved residues in the putative catalytic triad of human bile acid Coenzyme A:amino acid N-acyltransferase."

[9].
"Glycine and taurine conjugation of bile acids by a single enzyme. Molecular cloning and expression of human liver bile acid CoA:amino acid N-acyltransferase."

[10].
"Purification and characterization of bile acid-CoA:amino acid N-acyltransferase from human liver."
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