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Myosin 9 抗体 (pTyr158)

This anti-Myosin 9 antibody is a 兔 多克隆 antibody detecting Myosin 9 in DB. Suitable for 人. This Primary Antibody has been cited in 1 publication.
产品编号 ABIN1539741
发货至: 中国

Quick Overview for Myosin 9 抗体 (pTyr158) (ABIN1539741)

抗原

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

适用

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宿主

  • 52
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克隆类型

  • 52
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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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Dot Blot (DB)

克隆位点

RB36361
  • 抗原表位

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    pTyr158

    预测反应

    C, M, Rat

    纯化方法

    This antibody is purified through a protein A column, followed by peptide affinity purification.

    免疫原

    This MYH9 Antibody is generated from rabbits immunized with a KLH conjugated synthetic phosphopeptide corresponding to amino acid residues surrounding Y158 of human MYH9.

    亚型

    Ig Fraction
  • 应用备注

    DB: 1:500

    限制

    仅限研究用
  • 状态

    Liquid

    缓冲液

    Purified polyclonal antibody supplied in PBS with 0.09 % (W/V) sodium azide.

    储存液

    Sodium azide

    注意事项

    This product contains Sodium azide: 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

    Phospho-MYH9-Y158 Antibody can be refrigerated at 2-8 °C for up to 6 months. For long term storage, place the Phospho-MYH9-Y158 Antibody at -20 °C.

    有效期

    6 months
  • Almeida, Mesquita, Cruz, Osório, Custódio, Brito, Vingadassalom, Martins, Leong, Holden, Cabanes, Sousa: "Src-dependent tyrosine phosphorylation of non-muscle myosin heavy chain-IIA restricts Listeria monocytogenes cellular infection." in: The Journal of biological chemistry, Vol. 290, Issue 13, pp. 8383-95, (2015) (PubMed).

  • 抗原

    Myosin 9 (MYH9)

    别名

    MYH9

    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

    226532

    基因ID

    4627

    NCBI登录号

    NP_002464

    UniProt

    P35579

    途径

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