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CCDC174 抗体 (AA 1-100)

This anti-CCDC174 antibody is a 兔 多克隆 antibody detecting CCDC174 in WB, IF (cc), IF (p), ELISA, IHC (fro), IHC (p) 和 ICC. Suitable for 人.
产品编号 ABIN1713724
发货至: 中国

Quick Overview for CCDC174 抗体 (AA 1-100) (ABIN1713724)

抗原

CCDC174 (Coiled-Coil Domain Containing 174 (CCDC174))

适用

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宿主

  • 19

克隆类型

  • 19
多克隆

标记

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This CCDC174 antibody is un-conjugated

应用范围

Western Blotting (WB), Immunofluorescence (Cultured Cells) (IF (cc)), Immunofluorescence (Paraffin-embedded Sections) (IF (p)), ELISA, Immunohistochemistry (Frozen Sections) (IHC (fro)), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p)), Immunocytochemistry (ICC)
  • 抗原表位

    • 14
    • 3
    • 1
    • 1
    AA 1-100

    预测反应

    Human,Mouse,Rat

    纯化方法

    Purified by Protein A.

    免疫原

    KLH conjugated synthetic peptide derived from human C3orf19

    亚型

    IgG
  • 应用备注

    WB 1:300-5000
    ELISA 1:500-1000
    IHC-P 1:200-400
    IHC-F 1:100-500
    IF(IHC-P) 1:50-200
    IF(IHC-F) 1:50-200
    IF(ICC) 1:50-200
    ICC 1:100-500

    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

    CCDC174 (Coiled-Coil Domain Containing 174 (CCDC174))

    别名

    C3orf19

    背景

    Synonyms: Ccdc174, Coiled coil domain containing 174, Uncharacterized protein C3orf19, CC174_HUMAN.

    Background: Chromosome 3 is made up of about 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. The C3orf19 gene product has been provisionally designated C3orf19 pending further characterization.

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