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C7ORF25 抗体 (AA 1-100) (HRP)

This anti-C7ORF25 antibody is a 兔 多克隆 antibody detecting C7ORF25 in WB, ELISA, IHC (p) 和 IHC (fro). Suitable for 小鼠.
产品编号 ABIN1712215
发货至: 中国

Quick Overview for C7ORF25 抗体 (AA 1-100) (HRP) (ABIN1712215)

抗原

C7ORF25 (Chromosome 7 Open Reading Frame 25 (C7ORF25))

适用

  • 14
  • 9
小鼠

宿主

  • 23

克隆类型

  • 23
多克隆

标记

  • 5
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This C7ORF25 antibody is conjugated to HRP

应用范围

  • 23
  • 13
  • 13
  • 9
  • 8
  • 4
  • 2
  • 1
Western Blotting (WB), ELISA, Immunohistochemistry (Paraffin-embedded Sections) (IHC (p)), Immunohistochemistry (Frozen Sections) (IHC (fro))
  • 抗原表位

    • 14
    • 9
    • 2
    AA 1-100

    交叉反应

    小鼠

    预测反应

    Human,Rat,Dog,Cow,Sheep,Pig,Horse,Rabbit

    纯化方法

    Purified by Protein A.

    免疫原

    KLH conjugated synthetic peptide derived from human C7orf25

    亚型

    IgG
  • 应用备注

    WB 1:300-5000
    IHC-P 1:200-400
    IHC-F 1:100-500

    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

    C7ORF25 (Chromosome 7 Open Reading Frame 25 (C7ORF25))

    别名

    C7orf25

    背景

    Synonyms: C7orf25, CG025_HUMAN, Chromosome 7 open reading frame 25, RGD1308147, UPF0415 protein C7orf25.

    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 C7orf25 gene product has been provisionally designated C7orf25 pending further characterization.

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