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FZD9 抗体 (N-Term)

This anti-FZD9 antibody is a 兔 多克隆 antibody detecting FZD9 in WB 和 IHC (p). Suitable for 人.
产品编号 ABIN2857084
发货至: 中国

Quick Overview for FZD9 抗体 (N-Term) (ABIN2857084)

抗原

See all FZD9 抗体
FZD9 (Frizzled Family Receptor 9 (FZD9))

适用

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宿主

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克隆类型

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多克隆

标记

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This FZD9 antibody is un-conjugated

应用范围

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Western Blotting (WB), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))
  • 抗原表位

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    N-Term

    交叉反应

    小鼠, 大鼠

    交叉反应 (详细)

    Mouse (92 %), Rat (92 %)

    产品特性

    Rabbit Polyclonal antibody to Frizzled 9 (frizzled homolog 9 (Drosophila))
    Frizzled 9 antibody [N1N2], N-term

    纯化方法

    Purified by antigen-affinity chromatography.

    免疫原

    Carrier-protein conjugated synthetic peptide encompassing a sequence within the N-terminus region of human Frizzled 9. The exact sequence is proprietary.

    亚型

    IgG
  • 应用备注

    Suggested dilution Reference IHC (Formalin-fixed paraffin-embedded sections) 1:100-1:1000* Western blot 1:500-1:3000* Not tested in other applications. *Optimal dilutions/concentrations should be determined by the researcher.Suggested dilutionReferenceIHC (Formalin-fixed paraffin-embedded sections)1:100-1:1000* Western blot1:500-1:3000*

    说明

    Positive Control: U87-MG

    限制

    仅限研究用
  • 状态

    Liquid

    浓度

    0.77 mg/mL

    缓冲液

    0.1M Tris, 0.1M Glycine, 20 % Glycerol ( pH 7). 0.01 % Thimerosal was added as a preservative.

    储存液

    Thimerosal (Merthiolate)

    注意事项

    This product contains Thimerosal (Merthiolate): a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

    储存条件

    -20 °C

    储存方法

    Keep as concentrated solution. Aliquot and store at -20°C or below. Avoid multiple freeze-thaw cycles.
  • 抗原

    FZD9 (Frizzled Family Receptor 9 (FZD9))

    别名

    Frizzled 9

    背景

    Members of the 'frizzled' gene family encode 7-transmembrane domain proteins that are receptors for Wnt signaling proteins. The FZD9 gene is located within the Williams syndrome common deletion region of chromosome 7, and heterozygous deletion of the FZD9 gene may contribute to the Williams syndrome phenotype. FZD9 is expressed predominantly in brain, testis, eye, skeletal muscle, and kidney.

    Cellular Localization: Cell membrane, Multi-pass membrane protein

    分子量

    64 kDa

    基因ID

    8326

    途径

    WNT signaling
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