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CCDC12 抗体 (AA 19-120) (Biotin)

This anti-CCDC12 antibody is a 兔 多克隆 antibody detecting CCDC12 in WB, ELISA, IHC (fro) 和 IHC (p). Suitable for 人 和 大鼠.
产品编号 ABIN887070
发货至: 中国

Quick Overview for CCDC12 抗体 (AA 19-120) (Biotin) (ABIN887070)

抗原

See all CCDC12 抗体
CCDC12 (Coiled-Coil Domain Containing 12 (CCDC12))

适用

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人, 大鼠

宿主

  • 31
  • 1

克隆类型

  • 31
  • 1
多克隆

标记

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This CCDC12 antibody is conjugated to Biotin

应用范围

  • 25
  • 13
  • 13
  • 11
  • 2
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  • 1
Western Blotting (WB), ELISA, Immunohistochemistry (Frozen Sections) (IHC (fro)), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))
  • 抗原表位

    • 14
    • 8
    • 2
    • 1
    • 1
    • 1
    AA 19-120

    交叉反应

    人, 大鼠

    预测反应

    Mouse,Dog,Cow,Pig,Horse

    纯化方法

    Purified by Protein A.

    免疫原

    KLH conjugated synthetic peptide derived from human CCDC12

    亚型

    IgG
  • 应用备注

    WB 1:300-5000
    IHC-P 1:200-400
    IHC-F 1:100-500

    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

    CCDC12 (Coiled-Coil Domain Containing 12 (CCDC12))

    别名

    CCDC12

    背景

    Synonyms: Coiled-coil domain-containing protein 12, CCDC12

    Background: CCDC12, also known as FLJ39430, FLJ40801 or MGC23918, is a 166 amino acid protein encoded by a gene mapping to human chromosome 3. 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.

    基因ID

    151903

    UniProt

    Q8WUD4
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