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C3ORF14 抗体 (AA 1-100) (Cy7)

This anti-C3ORF14 antibody is a 兔 多克隆 antibody detecting C3ORF14 in WB, IF (cc) 和 IF (p). Suitable for 人.
产品编号 ABIN1707300
发货至: 中国

Quick Overview for C3ORF14 抗体 (AA 1-100) (Cy7) (ABIN1707300)

抗原

C3ORF14 (Chromosome 3 Open Reading Frame 14 (C3ORF14))

适用

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宿主

  • 21

克隆类型

  • 21
多克隆

标记

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This C3ORF14 antibody is conjugated to Cy7

应用范围

  • 17
  • 12
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  • 9
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Western Blotting (WB), Immunofluorescence (Cultured Cells) (IF (cc)), Immunofluorescence (Paraffin-embedded Sections) (IF (p))
  • 抗原表位

    • 14
    • 7
    AA 1-100

    预测反应

    Human

    纯化方法

    Purified by Protein A.

    免疫原

    KLH conjugated synthetic peptide derived from human C3orf14

    亚型

    IgG
  • 应用备注

    IF(IHC-P) 1:50-200
    IF(IHC-F) 1:50-200
    IF(ICC) 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

    C3ORF14 (Chromosome 3 Open Reading Frame 14 (C3ORF14))

    别名

    C3orf14

    背景

    Synonyms: C3orf14, CC014_HUMAN, chromosome 3 open reading frame 14, HT021, Uncharacterized protein C3orf14.

    Background: C3orf14 (chromosome 3 open reading frame 14), also known as HT021, is a 128 amino acid protein that is encoded by a gene mapping to human chromosome 3p14.2. 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.

    基因ID

    57415
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