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CCDC37 抗体 (AA 201-300) (HRP)

This anti-CCDC37 antibody is a Rabbit Polyclonal antibody detecting CCDC37 in WB, ELISA, IHC (p), IHC (fro). Suitable for Human.
产品编号 ABIN887657
发货至: 中国

Quick Overview for CCDC37 抗体 (AA 201-300) (HRP) (ABIN887657)

抗原

See all CCDC37 抗体
CCDC37 (Coiled-Coil Domain Containing 37 (CCDC37))

适用

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宿主

  • 34

克隆类型

  • 34
多克隆

标记

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This CCDC37 antibody is conjugated to HRP

应用范围

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

    • 14
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    AA 201-300

    预测反应

    Human

    纯化方法

    Purified by Protein A.

    免疫原

    KLH conjugated synthetic peptide derived from human CCDC37

    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.

    注意事项

    Do NOT add Sodium Azide! Use of Sodium Azide will inhibit enzyme activity of horseradish peroxidase.

    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

    CCDC37 (Coiled-Coil Domain Containing 37 (CCDC37))

    别名

    CCDC37

    背景

    Synonyms: CCD37_HUMAN, CCDC37, Coiled-coil domain containing 37, Coiled-coil domain-containing protein 37.

    Background: CCDC37 is a 611 amino acid protein that exists as two alternatively spliced isoforms. The gene encoding CCDC37 maps to human chromosome 3, which 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

    348807
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