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ARSA (基因名), Arylsulfatase A (蛋白名), arsa_human.
产品名称:

Human ARSA/ Arylsulfatase A Recombinant Protein
芳基硫酸酯酶A

货号:

R0256h

商标:
EIAab®
监管等级:
别名:

Cerebroside-sulfatase, ASA

序列号:
P15289
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:
Neurosciences
Human ARSA Protein
规格 & 价格: cart
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Human ARSA 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: 22q13.33 by HGNC 22q13.33 by Entrez Gene 22q13.33 by Ensembl
ARSA 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 at neutral pH and homooctamer at acidic pH. Exists both as a single chain of 58 kDa (component A) or as a chain of 50 kDa (component B) linked by disulfide bond(s) to a 7 kDa chain (component C). Interacts with SUMF1.


功能:
Hydrolyzes cerebroside sulfate.


亚细胞位置:
Lysosome


该产品尚未在任何出版物中被引用。

[1].
"Characterization of new arylsulfatase A gene mutations reinforces genotype-phenotype correlation in metachromatic leukodystrophy."

[2].
"Molecular analysis of ARSA and PSAP genes in twenty-one Italian patients with metachromatic leukodystrophy: identification and functional characterization of 11 novel ARSA alleles."

[3].
"Enzyme replacement improves nervous system pathology and function in a mouse model for metachromatic leukodystrophy."

[4].
"Mutations c.459+1G>A and p.P426L in the ARSA gene: prevalence in metachromatic leukodystrophy patients from European countries."

[5].
"Adult onset metachromatic leukodystrophy without electroclinical peripheral nervous system involvement: a new mutation in the ARSA gene."

[6].
"Late onset MLD with normal nerve conduction associated with two novel missense mutations in the ASA gene."

[7].
"Crystal structure of a covalent intermediate of endogenous human arylsulfatase A."

[8].
"Oligomerization capacity of two arylsulfatase A mutants: C300F and P425T."

[9].
"Croatian population data for arylsulfatase a pseudodeficiency-associated mutations in healthy subjects, and in patients with Alzheimer-type dementia and Down syndrome."

[10].
"Evidence for an N-glycosylation polymorphism of arylsulfatase a predisposing to alcoholism in Koreans."
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