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Ataxin 1 抗体

This anti-Ataxin 1 antibody is a 兔 多克隆 antibody detecting Ataxin 1 in WB, IHC 和 ELISA. Suitable for 小鼠, 人 和 大鼠.
产品编号 ABIN7249019
发货至: 中国
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中国
北京 101111
No. 88 KeChuang 6th Street
Beijing Economic Technological Development Area
Room 801-803
4A Biotech Co.,Ltd.
Tel +86 (0512) 65829739 传真 +86 (010) 6788 5057

Quick Overview for Ataxin 1 抗体 (ABIN7249019)

抗原

See all Ataxin 1 (ATXN1) 抗体
Ataxin 1 (ATXN1)

适用

  • 99
  • 61
  • 36
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
小鼠, 人, 大鼠

宿主

  • 73
  • 61
  • 1

克隆类型

  • 72
  • 63
多克隆

标记

  • 49
  • 9
  • 7
  • 7
  • 5
  • 4
  • 3
  • 3
  • 3
  • 3
  • 3
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
This Ataxin 1 antibody is un-conjugated

应用范围

  • 97
  • 51
  • 48
  • 46
  • 35
  • 33
  • 23
  • 23
  • 9
  • 8
  • 6
  • 1
  • 1
Western Blotting (WB), Immunohistochemistry (IHC), ELISA
  • 产品特性

    Polyclonal Antibody

    纯化方法

    Affinity purification

    免疫原

    Recombinant protein of human ATXN1

    亚型

    IgG
  • 应用备注

    WB 1:500-1:2000, IHC 1:50-1:200

    限制

    仅限研究用
  • 状态

    Liquid

    浓度

    0.3 mg/mL

    缓冲液

    PBS with 0.05 % sodium azide and 50 % glycerol, PH7.4

    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

    Store at -20°C. Avoid freeze / thaw cycles.
  • 抗原

    Ataxin 1 (ATXN1)

    别名

    ATXN1

    背景

    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. ADCAI is genetically heterogeneous, with five genetic loci, designated spinocerebellar ataxia (SCA) 1, 2, 3, 4 and 6, being assigned to five different chromosomes. ADCAII, which always presents with retinal degeneration (SCA7), and ADCAIII often referred to as the `pure' cerebellar syndrome (SCA5), are most likely homogeneous disorders. Several SCA genes have been cloned and shown to contain CAG repeats in their coding regions.

    分子量

    87 kDa

    UniProt

    P54253

    途径

    Synaptic Membrane
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