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C3orf37 抗体

This anti-C3orf37 antibody is a 兔 多克隆 antibody detecting C3orf37 in WB, IF (p) 和 IHC (p). Suitable for 人, 小鼠 和 大鼠.
产品编号 ABIN1387187
发货至: 中国

Quick Overview for C3orf37 抗体 (ABIN1387187)

抗原

See all C3orf37 (C3ORF37) 抗体
C3orf37 (C3ORF37) (Chromosome 3 Open Reading Frame 37 (C3ORF37))

适用

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  • 3
  • 2
  • 2
  • 2
  • 2
  • 1
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人, 小鼠, 大鼠

宿主

  • 28

克隆类型

  • 28
多克隆

标记

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  • 2
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  • 2
  • 1
  • 1
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  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
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This C3orf37 antibody is un-conjugated

应用范围

  • 28
  • 12
  • 7
  • 2
  • 1
  • 1
Western Blotting (WB), Immunofluorescence (Paraffin-embedded Sections) (IF (p)), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))
  • 交叉反应

    人, 小鼠, 大鼠

    纯化方法

    Purified by Protein A.

    免疫原

    KLH conjugated synthetic peptide derived from human C3orf37

    亚型

    IgG
  • 应用备注

    WB 1:300-5000
    IHC-P 1:200-400
    IF(IHC-P) 1:50-200

    限制

    仅限研究用
  • 状态

    Liquid

    浓度

    1 μg/μL

    缓冲液

    0.01M TBS( pH 7.4) with 1 % BSA, 0.02 % Proclin300 and 50 % Glycerol.

    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

    Shipped at 4°C. Store at -20°C for one year. Avoid repeated freeze/thaw cycles.

    有效期

    12 months
  • 抗原

    C3orf37 (C3ORF37) (Chromosome 3 Open Reading Frame 37 (C3ORF37))

    别名

    C3orf37

    背景

    Synonyms: C3orf37, CC037_HUMAN, Chromosome 3 open reading frame 37, DC12, MGC111075, UPF0361 protein C3orf37.

    Background: C3orf37, also known as DC12 or MGC111075, is a 354 amino acid protein encoded by a gene that maps to human chromosome 3q21.3. Chromosome 3 is made up of approximately 214 million bases encoding over 1,100 genes. Notably, there is a chemokine receptor gene cluster and a variety of human cancer related loci on chromosome 3. Particular regions of the chromosome 3 short arm are deleted in many types of cancer cells. Key tumor suppressing genes on chromosome 3 encode apoptosis mediator RASSF1, cell migration regulator HYAL1 and angiogenesis suppressor SEMA3B. Marfan Syndrome, porphyria, von Hippel-Lindau syndrome, osteogenesis imperfecta and Charcot-Marie-Tooth disease are a few of the numerous genetic diseases associated with chromosome 3.

    基因ID

    56941
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