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ATXN2 (基因名), Ataxin-2 (蛋白名), atx2_human.
产品名称:

Human ATXN2/ Ataxin-2 Recombinant Protein

货号:

R15645h

商标:
EIAab®
监管等级:
别名:

Spinocerebellar ataxia type 2 protein, Trinucleotide repeat-containing gene 13 protein, ATX2, SCA2, TNRC13

序列号:
Q99700
来源:
E.coli
种属:
Human
标签:
His
序列:
431-630aa
预估分子量:
22.00 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:
Neurosciences
Human ATXN2 Protein
规格 & 价格: cart
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Human ATXN2 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
Human ATXN2 Protein
Recombinant human ATXN2 protein was determined by 12% SDS-PAGE stained with Coomassie Blue under reducing conditions.
基因位点
Cytogenetic band: 12q24.12 by HGNC 12q24.12 by Entrez Gene 12q24.12 by Ensembl
ATXN2 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 (By similarity). Can also form homodimers (By similarity). Interacts with TARDBP; the interaction is RNA-dependent (PubMed:20740007). Interacts with RBFOX1 (PubMed:10814712). Interacts with polyribosomes (PubMed:16835262). Interacts with SH3GL2 and SH3GL3 (PubMed:18602463). Interacts with SH3KBP1 and CBL (By similarity). Interacts with EGFR (PubMed:18602463). Interacts with ATXN2L (PubMed:23209657).


功能:
Involved in EGFR trafficking, acting as negative regulator of endocytic EGFR internalization at the plasma membrane.


亚细胞位置:
Cytoplasm


该产品尚未在任何出版物中被引用。

[1].
"Genetic variance in the spinocerebellar ataxia type 2 (ATXN2) gene in children with severe early onset obesity."

[2].
"Screening for premutation in the FMR1 gene in male patients suspected of spinocerebellar ataxia."

[3].
"Ataxin-2 associates with the endocytosis complex and affects EGF receptor trafficking."

[4].
"Lack of mutations in spinocerebellar ataxia type 2 and 3 genes in a Taiwanese (ethnic Chinese) cohort of familial and early-onset parkinsonism."

[5].
"Ataxin-2 and its Drosophila homolog, ATX2, physically assemble with polyribosomes."

[6].
"Molecular genetics of hereditary spinocerebellar ataxia: mutation analysis of spinocerebellar ataxia genes and CAG/CTG repeat expansion detection in 225 Italian families."

[7].
"A novel protein with RNA-binding motifs interacts with ataxin-2."

[8].
"Genomic structure of the human gene for spinocerebellar ataxia type 2 (SCA2) on chromosome 12q24.1."

[9].
"Identification of the spinocerebellar ataxia type 2 gene using a direct identification of repeat expansion and cloning technique, DIRECT."

[10].
"Ataxin-2-like is a regulator of stress granules and processing bodies."
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