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C7orf64 抗体 (AA 1-100)

This anti-C7orf64 antibody is a 兔 多克隆 antibody detecting C7orf64 in WB, IF (cc), IF (p), ELISA, IHC (fro), IHC (p) 和 ICC. Suitable for 人.
产品编号 ABIN1714045
发货至: 中国

Quick Overview for C7orf64 抗体 (AA 1-100) (ABIN1714045)

抗原

See all C7orf64 抗体
C7orf64 (Chromosome 7 Open Reading Frame 64 (C7orf64))

适用

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宿主

  • 27

克隆类型

  • 27
多克隆

标记

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This C7orf64 antibody is un-conjugated

应用范围

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

    • 14
    • 7
    • 2
    • 1
    • 1
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    • 1
    • 1
    AA 1-100

    交叉反应

    预测反应

    Mouse,Rat,Dog,Cow,Sheep,Horse,Chicken,Rabbit

    纯化方法

    Purified by Protein A.

    免疫原

    KLH conjugated synthetic peptide derived from human C7orf64

    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

    C7orf64 (Chromosome 7 Open Reading Frame 64 (C7orf64))

    别名

    C7orf64

    背景

    Synonyms: C7orf64, RBM48_HUMAN, DKFZP564O0523, DKFZp686D1651, HSPC304, Hypothetical protein LOC84060, OTTHUMP00000215752, UPF0712 protein C7orf64.

    Background: Chromosome 7 has been linked to Osteogenesis imperfecta, Pendred syndrome, Lissencephaly, Citrullinemia and Shwachman-Diamond syndrome. The deletion of a portion of the q arm of chromosome 7 is associated with Williams-Beuren syndrome, a condition characterized by mild mental retardation, an unusual comfort and friendliness with strangers and an elfin appearance. Deletions of portions of the q arm of chromosome 7 are also seen in a number of myeloid disorders including cases of acute myelogenous leukemia and myelodysplasia. The C7orf64 gene product has been provisionally designated C7orf64 pending further characterization.

    基因ID

    84060
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