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Myosin 9 抗体 (N-Term)

This anti-Myosin 9 antibody is a 兔 多克隆 antibody detecting Myosin 9 in WB, IF, IP, IHC (p) 和 ICC. Suitable for 人.
产品编号 ABIN2855153
发货至: 中国

Quick Overview for Myosin 9 抗体 (N-Term) (ABIN2855153)

抗原

See all Myosin 9 (MYH9) 抗体
Myosin 9 (MYH9)

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 Myosin 9 antibody is un-conjugated

应用范围

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Western Blotting (WB), Immunofluorescence (IF), Immunoprecipitation (IP), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p)), Immunocytochemistry (ICC)

质量等级

KO Validated
  • 抗原表位

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    N-Term

    特异性

    This antibody may cross react with MYH10, MYH14, or other family members.

    交叉反应

    产品特性

    Rabbit Polyclonal antibody to MYH9 (myosin, heavy chain 9, non-muscle)
    MYH9 antibody [N1], N-term

    纯化方法

    Purified by antigen-affinity chromatography.

    免疫原

    Recombinant protein encompassing a sequence within the N-terminus region of human MYH9. The exact sequence is proprietary.

    亚型

    IgG
  • 应用备注

    WB: 1:500-1:3000. IHC-P: 1:100-1:1000. IP: 1:100-1:500. Optimal dilutions/concentrations should be determined by the researcher. Not tested in other applications.

    说明

    Positive Control: U87-MG , SK-N-SH , IMR32 , SK-N-AS , NT2D1 , PC-3

    Validation: KO/KD, Overexpression

    限制

    仅限研究用
  • 状态

    Liquid

    浓度

    1.31 mg/mL

    缓冲液

    1XPBS pH 7, 20 % Glycerol, 0.025 % ProClin 300

    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

    Store as concentrated solution. Centrifuge briefly prior to opening vial. For short-term storage (1-2 weeks), store at 4°C. For long-term storage, aliquot and store at -20°C or below. Avoid multiple freeze-thaw cycles.
  • 抗原

    Myosin 9 (MYH9)

    别名

    myosin heavy chain 9

    背景

    This gene encodes a myosin IIA heavy chain that contains an IQ domain and a myosin head-like domain. The protein is involved in several important functions, including cytokinesis, cell motility and maintenance of cell shape. Defects in MYH9 are the cause of non-syndromic sensorineural deafness autosomal dominant type 17, Epstein syndrome, Alport syndrome with macrothrombocytopenia, Sebastian syndrome, Fechtner syndrome and macrothrombocytopenia with progressive sensorineural deafness.

    分子量

    227 kDa

    基因ID

    4627

    UniProt

    P35579

    途径

    Regulation of G-Protein Coupled Receptor Protein Signaling, Integrin Complex
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