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C20orf78 抗体 (AA 21-100)

This anti-C20orf78 antibody is a 兔 多克隆 antibody detecting C20orf78 in ELISA, ICC, IF (cc), IF (p), IHC (fro) 和 IHC (p). Suitable for 人.
产品编号 ABIN1713398
发货至: 中国

Quick Overview for C20orf78 抗体 (AA 21-100) (ABIN1713398)

抗原

C20orf78 (C20ORF78) (Chromosome 20 Open Reading Frame 78 (C20ORF78))

适用

宿主

克隆类型

多克隆

应用范围

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

    AA 21-100

    预测反应

    Human

    纯化方法

    Purified by Protein A.

    免疫原

    KLH conjugated synthetic peptide derived from human c20orf78

    亚型

    IgG
  • 应用备注

    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

    C20orf78 (C20ORF78) (Chromosome 20 Open Reading Frame 78 (C20ORF78))

    别名

    c20orf78

    背景

    Synonyms: C20orf78, Chromosome 20 open reading frame 78, CT078_HUMAN, dJ1068E13.1, Putative uncharacterized protein C20orf78.

    Background: Representing about 2 % of human DNA, chromosome 20 consists of approximately 63 million bases and 600 genes. Chromosome 20 contains a region with numerous genes expressed in the epididymis, which are thought important for seminal production, and some viewed as 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. Amyotrophic lateral sclerosis, spinal muscular atrophy, ring chromosome 20 epilepsy syndrome and Alagille syndrome are also associated with chromosome 20. The C20orf78 gene product has been provisionally designated C20orf78 pending further characterization.

    基因ID

    100128496
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