电话:
+86 (0512) 65829739
传真:
+86 (010) 6788 5057
电子邮件:
orders@antibodies-online.cn

Ataxin 2 抗体

This anti-Ataxin 2 antibody is a 兔 多克隆 antibody detecting Ataxin 2 in WB, IP 和 IHC (p). Suitable for 人.
产品编号 ABIN7464185
发货至: 中国

Quick Overview for Ataxin 2 抗体 (ABIN7464185)

抗原

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

适用

  • 24
  • 23
  • 5
  • 4
  • 3
  • 3
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1

宿主

  • 37
  • 1
  • 1

克隆类型

  • 39
多克隆

标记

  • 21
  • 3
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This Ataxin 2 antibody is un-conjugated

应用范围

  • 34
  • 15
  • 13
  • 13
  • 6
  • 5
  • 4
  • 4
  • 3
  • 2
  • 2
Western Blotting (WB), Immunoprecipitation (IP), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))

质量等级

KO Validated
  • 交叉反应

    人, 小鼠

    纯化方法

    Purified by antigen-affinity chromatography.

    免疫原

    Recombinant protein encompassing a sequence within the center region of human ATXN2. The exact sequence is proprietary.

    亚型

    IgG
  • 应用备注

    WB: 1:500-1:3000. IHC-P: 1:100-1:1000. Optimal dilutions/concentrations should be determined by the researcher. Not tested in other applications.

    说明

    Positive Control: 293T , A431 , HeLa , HepG2

    Validation: KO/KD

    限制

    仅限研究用
  • 状态

    Liquid

    浓度

    0.28 mg/mL

    缓冲液

    1XPBS ( pH 7), 20 % Glycerol, 0.025 % ProClin 300

    储存液

    ProClin

    注意事项

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

    储存条件

    4 °C,-20 °C

    储存方法

    Store as concentrated solution. Centrifuge briefly prior to opening vial. For short-term storage (1-2 weeks), store at 4°C. For long-term storage, aliquot and store at -20°C or below. Avoid multiple freeze-thaw cycles.
  • 抗原

    Ataxin 2 (ATXN2)

    别名

    ataxin 2

    背景

    Ataxin 2 , ATX2 , SCA2 , TNRC13,The autosomal dominant cerebellar ataxias (ADCA) are a heterogeneous group of neurodegenerative disorders characterized by progressive degeneration of the cerebellum, brain stem and spinal cord. Clinically, ADCA has been divided into three groups: ADCA types I-III. Defects in this gene are the cause of spinocerebellar ataxia type 2 (SCA2). SCA2 belongs to the autosomal dominant cerebellar ataxias type I (ADCA I) which are characterized by cerebellar ataxia in combination with additional clinical features like optic atrophy, ophthalmoplegia, bulbar and extrapyramidal signs, peripheral neuropathy and dementia. SCA2 is caused by expansion of a CAG repeat in the coding region of this gene. Longer expansions result in earlier onset of the disease. Alternatively spliced transcript variants encoding different isoforms have been identified but their full length sequence has not been determined. [provided by RefSeq]

    分子量

    140 kDa

    基因ID

    6311

    UniProt

    Q99700

    途径

    Ribonucleoprotein Complex Subunit Organization
You are here:
Chat with us!