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C3ORF70 抗体 (Cy7)

This anti-C3ORF70 antibody is a 兔 多克隆 antibody detecting C3ORF70 in WB 和 IF (p). Suitable for 人, 小鼠 和 大鼠.
产品编号 ABIN1423100
发货至: 中国

Quick Overview for C3ORF70 抗体 (Cy7) (ABIN1423100)

抗原

C3ORF70 (Chromosome 3 Open Reading Frame 70 (C3ORF70))

适用

  • 16
  • 15
  • 15
  • 2
  • 2
  • 1
  • 1
人, 小鼠, 大鼠

宿主

  • 16

克隆类型

  • 16
多克隆

标记

  • 3
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
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This C3ORF70 antibody is conjugated to Cy7

应用范围

  • 16
  • 12
  • 3
Western Blotting (WB), Immunofluorescence (Paraffin-embedded Sections) (IF (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 C3orf70

    亚型

    IgG
  • 应用备注

    IF(IHC-P) 1:50-200

    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. Aliquot into multiple vials to avoid repeated freeze-thaw cycles.

    有效期

    12 months
  • 抗原

    C3ORF70 (Chromosome 3 Open Reading Frame 70 (C3ORF70))

    别名

    C3orf70

    背景

    Synonyms: C3orf70, CC070_HUMAN, Chromosome 3 open reading frame 70, hypothetical protein LOC285, UPF0524 protein C3orf70.

    Background: C3orf70 is a 250 amino acid protein that belongs to the UPF0524 family and is encoded by a gene that maps to human chromosome 3q27.2. 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.

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