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C18orf56 抗体 (HRP)

This HRP-conjugated 兔 多克隆 anti-C18orf56 antibody specifically detects C18orf56 in WB 和 IHC (p). The antibody is reactive with 人 samples.
产品编号 ABIN1421890
发货至: 中国
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Quick Overview for C18orf56 抗体 (HRP) (ABIN1421890)

抗原

C18orf56 (Chromosome 18 Open Reading Frame 56 (C18orf56))

适用

宿主

  • 15

克隆类型

  • 15
多克隆

标记

  • 2
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This C18orf56 antibody is conjugated to HRP

应用范围

  • 15
  • 13
  • 2
Western Blotting (WB), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))
  • 交叉反应

    纯化方法

    Purified by Protein A.

    免疫原

    KLH conjugated synthetic peptide derived from human C18orf56

    亚型

    IgG
  • 应用备注

    WB 1:300-5000
    IHC-P 1:200-400

    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

    C18orf56 (Chromosome 18 Open Reading Frame 56 (C18orf56))

    别名

    C18orf56

    背景

    Synonyms: Putative uncharacterized protein C18orf56, CR056_HUMAN.

    Background: Encoding over 300 genes, chromosome 18 contains about 76 million bases. Trisomy 18, or Edwards syndrome, is the second most common trisomy after Downs syndrome. Symptoms of Edwards syndrome include low birth weight, a variety of physical development defects, heart deformations and breathing difficulty. Translocation between chromosome 18 and 14 is the most common translocation in cancers, and occurs in follicular lymphomas. Niemann-Pick disease, hereditary hemorrhagic telangiectasia and erythropoietic protoporphyria are associated with chromosome 18. The TGF_ modulators, Smad2, Smad4 and Smad7 are encoded by chromosome 18. The C18orf56 gene product has been provisionally designated C18orf56 pending further characterization.

    基因ID

    494514
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