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SNX29 抗体

RUNDC2A 适用: 人 IHC, ELISA 宿主: 兔 Polyclonal unconjugated
产品编号 ABIN7192586
发货至: 中国
  • 抗原 See all SNX29 (RUNDC2A) products
    SNX29 (RUNDC2A) (RUN Domain Containing 2A (RUNDC2A))
    适用
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    宿主
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    克隆类型
    • 28
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    多克隆
    标记
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    This SNX29 antibody is un-conjugated
    应用范围
    • 22
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    Immunohistochemistry (IHC), ELISA
    交叉反应
    人, 小鼠
    纯化方法
    Antigen affinity purification
    免疫原
    Synthetic peptide of Human SNX29
    亚型
    IgG
  • 应用备注
    ELISA:1:1000-1:2000, IHC:1:20-1:100,
    限制
    仅限研究用
  • 状态
    Liquid
    缓冲液
    -20 °C, pH 7.4 PBS, 0.05 % Sodium azide, 40 % Glycerol
    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,-80 °C
    储存方法
    Upon receipt, store at -20°C or -80°C. Avoid repeated freeze.
  • 抗原
    SNX29 (RUNDC2A) (RUN Domain Containing 2A (RUNDC2A))
    别名
    SNX29 (RUNDC2A 产品)
    别名
    RUNDC2A antibody, 4933437K13Rik antibody, ENSMUSG00000079738 antibody, Gm11170 antibody, Gm1737 antibody, Gm930 antibody, Rundc2a antibody, RGD1565890 antibody, A-388D4.1 antibody, RUN domain containing 2A antibody, sorting nexin 29 antibody, sorting nexin-29 antibody, RUNDC2A antibody, Snx29 antibody, SNX29 antibody, LOC104975843 antibody
    背景

    Background: SNX29 also known as RUNDC2A, is a 375 amino protein that contains one RUN domain. RUNDC2A is encoded by a gene that maps to human chromosome 16p13.13, which encodes over 900 genes and comprises nearly 3 % of the human genome. The GAN gene is located on chromosome 16 and, with mutation, may lead to giant axonal neuropathy, a nervous system disorder characterized by increasing malfunction with growth. The rare disorder Rubinstein-Taybi syndrome is also associated with chromosome 16, as is Crohn's disease, which is a gastrointestinal inflammatory condition.

    Aliases: SNX29 antibody, RUNDC2A antibody, Sorting nexin-29 antibody, RUN domain-containing protein 2A antibody

    UniProt
    Q8TEQ0
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