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ACY1 (基因名), Aminoacylase-1 (蛋白名), acy1_human.
产品名称:

Human ACY1/ Aminoacylase-1 Recombinant Protein
氨基酰化酶-1

货号:

R2259h

商标:
EIAab®
监管等级:
别名:

N-acyl-L-amino-acid amidohydrolase, ACY-1

序列号:
Q03154
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 ACY1 Protein
规格 & 价格: cart
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Human ACY1 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: 3p21.2 by HGNC 3p21.2 by Entrez Gene 3p21.2 by Ensembl
ACY1 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:
Homodimer. Interacts with SPHK1.


功能:
Involved in the hydrolysis of N-acylated or N-acetylated amino acids (except L-aspartate).


亚细胞位置:
Cytoplasm


该产品尚未在任何出版物中被引用。

[1].
"Neurological findings in aminoacylase 1 deficiency."

[2].
"Mutations in ACY1, the gene encoding aminoacylase 1, cause a novel inborn error of metabolism."

[3].
"Aminoacylase I deficiency: a novel inborn error of metabolism."

[4].
"Essential roles of zinc ligation and enzyme dimerization for catalysis in the aminoacylase-1/M20 family."

[5].
"The nucleotide sequence of human aminoacylase-1."

[6].
"Human aminoacylase-1. Cloning, sequence, and expression analysis of a chromosome 3p21 gene inactivated in small cell lung cancer."

[7].
"Human aminoacylase-1: cloning, regional assignment to distal chromosome 3p21.1, and identification of a cross-hybridizing sequence on chromosome 18."

[8].
"The molecular basis of aminoacylase 1 deficiency."

[9].
"Probing the acyl-binding pocket of aminoacylase-1."

[10].
"NMR spectroscopy of aminoacylase 1 deficiency, a novel inborn error of metabolism."
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