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Ataxin 2 抗体

This anti-Ataxin 2 antibody is a 兔 多克隆 antibody detecting Ataxin 2 in WB, ELISA, IHC, IF 和 IP. Suitable for 人, 小鼠 和 大鼠.
产品编号 ABIN7111771
发货至: 中国

Quick Overview for Ataxin 2 抗体 (ABIN7111771)

抗原

See all Ataxin 2 (ATXN2) 抗体
Ataxin 2 (ATXN2)

适用

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人, 小鼠, 大鼠

宿主

  • 38
  • 1
  • 1

克隆类型

  • 40
多克隆

标记

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This Ataxin 2 antibody is un-conjugated

应用范围

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Western Blotting (WB), ELISA, Immunohistochemistry (IHC), Immunofluorescence (IF), Immunoprecipitation (IP)
  • 纯化方法

    Immunogen affinity purified

    纯度

    ≥95 % as determined by SDS-PAGE

    免疫原

    ataxin 2

    亚型

    IgG
  • 应用备注

    WB: 1:1000-1:4000, IP: 1:500-1:2000, IHC: 1:20-1:200, IF: 1:10-1:100

    限制

    仅限研究用
  • 状态

    Liquid

    缓冲液

    PBS with 0.02 % sodium azide and 50 % glycerol pH 7.3,

    储存液

    Sodium azide

    注意事项

    This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

    储存条件

    -20 °C

    储存方法

    -20°C for 12 months (Avoid repeated freeze / thaw cycles.)

    有效期

    12 months
  • 抗原

    Ataxin 2 (ATXN2)

    别名

    Ataxin 2

    背景

    Synonyms:ataxin 2, ATX2, ATXN2, SCA2, TNRC13 Background:This gene belongs to a group of genes that is associated with microsatellite-expansion diseases, a class of neurological and neuromuscular disorders caused by expansion of short stretches of repetitive DNA. The protein encoded by this gene has two globular domains near the N-terminus, one of which contains a clathrin-mediated trans-Golgi signal and an endoplasmic reticulum exit signal. The encoded cytoplasmic protein localizes to the endoplasmic reticulum and plasma membrane, is involved in endocytosis, and modulates mTOR signals, modifying ribosomal translation and mitochondrial function. The N-terminal region of the protein contains a polyglutamine tract of 14-31 residues that can be expanded in the pathogenic state to 32-200 residues. Intermediate length expansions of this tract increase susceptibility to amyotrophic lateral sclerosis, while long expansions of this tract result in spinocerebellar ataxia-2, an autosomal-dominantly inherited, neurodegenerative disorder. Genome-wide association studies indicate that loss-of-function mutations in this gene may be associated with susceptibility to type I diabetes, obesity and hypertension. Alternative splicing results in multiple transcript variants.

    分子量

    140-150 kDa

    基因ID

    6311

    UniProt

    Q99700

    途径

    Ribonucleoprotein Complex Subunit Organization
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