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C9orf78 抗体 (AA 21-120)

This anti-C9orf78 antibody is a 兔 多克隆 antibody detecting C9orf78 in WB, IF (cc), IF (p), ELISA, IHC (p), ICC 和 IHC (fro). Suitable for 人.
产品编号 ABIN1714707
发货至: 中国

Quick Overview for C9orf78 抗体 (AA 21-120) (ABIN1714707)

抗原

C9orf78 (C9orf98) (Chromosome 9 Open Reading Frame 78 (C9orf98))

适用

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宿主

  • 21

克隆类型

  • 21
多克隆

标记

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This C9orf78 antibody is un-conjugated

应用范围

  • 20
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Western Blotting (WB), Immunofluorescence (Cultured Cells) (IF (cc)), Immunofluorescence (Paraffin-embedded Sections) (IF (p)), ELISA, Immunohistochemistry (Paraffin-embedded Sections) (IHC (p)), Immunocytochemistry (ICC), Immunohistochemistry (Frozen Sections) (IHC (fro))
  • 抗原表位

    • 14
    • 2
    • 1
    • 1
    • 1
    AA 21-120

    预测反应

    Human,Mouse,Rat,Dog,Cow,Pig,Horse

    纯化方法

    Purified by Protein A.

    免疫原

    KLH conjugated synthetic peptide derived from human C9orf78

    亚型

    IgG
  • 应用备注

    WB 1:300-5000
    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

    C9orf78 (C9orf98) (Chromosome 9 Open Reading Frame 78 (C9orf98))

    别名

    C9orf78

    背景

    Synonyms: bA409K20.3, C9orf78, Chromosome 9 open reading frame 78, CI078_HUMAN, HCA59, Hepatocellular carcinoma associated antigen 59, Hepatocellular carcinoma-associated antigen 59, HSPC220, Uncharacterized protein C9orf78.

    Background: Chromosome 9 consists of about 145 million bases and 4 % of the human genome and encodes nearly 900 genes. Considered to play a role in gender determination, deletion of the distal portion of 9p can lead to development of male to female sex reversal, the phenotype of a female with a male X,Y genotype. Hereditary hemorrhagic telangiectasia, which is characterized by harmful vascular defects, is associated with the chromosome 9 gene encoding endoglin protein, ENG. Familial dysautonomia is also associated with chromosome 9 though through the gene IKBKAP. Notably, chromosome 9 encompasses the largest interferon family gene cluster. Chromosome 9 is partnered with chromosome 22 in the translocation leading to the aberrant production of BCR-ABL fusion protein often found in leukemias. The C9orf78 gene product has been provisionally designated C9orf78 pending further characterization.

    基因ID

    51759
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