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C3orf24 抗体 (Biotin)

This anti-C3orf24 antibody is a 兔 多克隆 antibody detecting C3orf24 in WB 和 IHC (p). Suitable for 人, 大鼠 和 小鼠.
产品编号 ABIN1404871
发货至: 中国
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Quick Overview for C3orf24 抗体 (Biotin) (ABIN1404871)

抗原

See all C3orf24 抗体
C3orf24 (Chromosome 3 Open Reading Frame 24 (C3orf24))

适用

  • 18
  • 18
  • 17
  • 4
  • 4
  • 4
  • 3
  • 3
  • 2
  • 2
  • 1
  • 1
人, 大鼠, 小鼠

宿主

  • 18

克隆类型

  • 18
多克隆

标记

  • 5
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This C3orf24 antibody is conjugated to Biotin

应用范围

  • 18
  • 13
  • 2
Western Blotting (WB), 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 C3orf24

    亚型

    IgG
  • 应用备注

    WB 1:300-5000
    IHC-P 1:200-400

    限制

    仅限研究用
  • 状态

    Liquid

    浓度

    1 μg/μL

    缓冲液

    Aqueous buffered solution containing 0.01M TBS ( pH 7.4) with 1 % BSA, 0.03 % 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

    -20 °C

    储存方法

    Store at -20°C for 12 months.

    有效期

    12 months
  • 抗原

    C3orf24 (Chromosome 3 Open Reading Frame 24 (C3orf24))

    别名

    C3orf24

    背景

    Synonyms: C3orf24, CC024_HUMAN, chromosome 3 open reading frame 24, HSD19, hypothetical protein LOC115795, MGC40179, Uncharacterized protein C3orf24.

    Background: C3orf24, also known as MGC40179, is a 177 amino acid protein that is encoded by a gene that maps to human chromosome 3p25.3. 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

    115795
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