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BUD31 抗体

The 兔 多克隆 anti-BUD31 antibody is suitable to detect BUD31 in samples from 人, 大鼠 和 小鼠. It has been validated for WB, ELISA 和 IHC.
产品编号 ABIN7246052
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 BUD31 抗体 (ABIN7246052)

抗原

See all BUD31 抗体
BUD31 (BUD31 Homolog (BUD31))

适用

  • 56
  • 31
  • 22
  • 5
  • 5
  • 5
  • 4
  • 4
  • 4
  • 2
  • 2
  • 2
  • 2
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  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
人, 大鼠, 小鼠

宿主

  • 52
  • 4

克隆类型

  • 44
  • 12
多克隆

标记

  • 29
  • 4
  • 3
  • 3
  • 3
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  • 3
  • 3
  • 2
  • 1
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This BUD31 antibody is un-conjugated

应用范围

  • 35
  • 19
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  • 10
  • 7
  • 5
  • 2
  • 1
  • 1
  • 1
Western Blotting (WB), ELISA, Immunohistochemistry (IHC)
  • 产品特性

    Polyclonal Antibody

    纯化方法

    Antigen affinity purification

    免疫原

    Full length fusion protein

    亚型

    IgG
  • 应用备注

    WB 1:1000-1:5000, IHC 1:50-1:300, ELISA 1:5000-1:10000

    限制

    仅限研究用
  • 状态

    Liquid

    浓度

    1.5 mg/mL

    缓冲液

    PBS with 0.05 % Sodium azide and 40 % Glycerol, pH 7.4

    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

    BUD31 (BUD31 Homolog (BUD31))

    别名

    BUD31

    背景

    BUD31 (Protein G10 homolog, EDG-2) is a 144 amino acid protein encoded by the human gene BUD31. BUD31 is a nuclear protein that belongs to the BUD31 (G10) family. BUD31 is found on chromosome 7 which is about 158 milllion bases long, encodes over 1,000 genes and makes up about 5 % of the human genome. Chromosome 7 has been linked to osteogenesis imperfecta, Pendred syndrome, lissencephaly, citrullinemia and Shwachman-Diamond syndrome. The deletion of a portion of the long (q) arm of human chromosome 7 is associated with Williams-Beuren syndrome, a condition characterized by mild mental retardation, an unusual comfort and friendliness with strangers and an elfin appearance. Deletions of portions of the q arm of chromosome 7 are also seen in a number of myeloid disorders including cases of acute myelogenous leukemia and myelodysplasia.

    分子量

    Observed_MW: Refer to figures

    Calculated_MW: 17 kDa

    UniProt

    P41223
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