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C20orf141 抗体 (HRP)

This anti-C20orf141 antibody is a 兔 多克隆 antibody detecting C20orf141 in WB 和 IHC (p). Suitable for 人.
产品编号 ABIN1421980
发货至: 中国

Quick Overview for C20orf141 抗体 (HRP) (ABIN1421980)

抗原

C20orf141 (Chromosome 20 Open Reading Frame 141 (C20orf141))

适用

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宿主

  • 19

克隆类型

  • 19
多克隆

标记

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This C20orf141 antibody is conjugated to HRP

应用范围

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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 C20ORF141

    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

    C20orf141 (Chromosome 20 Open Reading Frame 141 (C20orf141))

    别名

    C20ORF141

    背景

    Synonyms: LOC128653, Chromosome 20 open reading frame 141, CT141_HUMAN.

    Background: The gene encoding C20orf141 maps to human chromosome 20, which houses over 600 genes, some of which are associated with Creutzfeldt-Jakob disease, amyotrophic lateral sclerosis, spinal muscular atrophy, ring chromosome 20 epilepsy syndrome and Alagille syndrome. Additionally, chromosome 20 contains a region with numerous genes which are thought important for seminal production and may be potential targets for male contraception. The PRNP gene encoding the prion protein associated with spongiform encephalopathies, like Creutzfeldt-Jakob disease, is found on chromosome 20. The C20orf141 gene product has been provisionally designated C20orf141 pending further characterization.

    基因ID

    128653
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