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Myosin 9 抗体 (C-Term)

This anti-Myosin 9 antibody is a 兔 多克隆 antibody detecting Myosin 9 in WB. Suitable for 人 和 小鼠.
产品编号 ABIN5534550
发货至: 中国

Quick Overview for Myosin 9 抗体 (C-Term) (ABIN5534550)

抗原

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

适用

  • 67
  • 14
  • 11
  • 3
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
人, 小鼠

宿主

  • 53
  • 12
  • 2
  • 1
  • 1

克隆类型

  • 53
  • 16
多克隆

标记

  • 43
  • 5
  • 5
  • 5
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This Myosin 9 antibody is un-conjugated

应用范围

  • 48
  • 38
  • 19
  • 14
  • 11
  • 10
  • 9
  • 8
  • 2
  • 2
  • 1
  • 1
Western Blotting (WB)
  • 抗原表位

    • 8
    • 7
    • 6
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    • 3
    • 3
    • 3
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 1840-1867, C-Term

    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 peptide between 1840-1867 amino acids from the C-terminal region of human MYH9.

    亚型

    Ig Fraction
  • 应用备注

    For WB starting dilution is: 1:2000

    限制

    仅限研究用
  • 状态

    Liquid

    浓度

    0.46 mg/mL

    缓冲液

    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

    Store at 4°C for three months and -20°C, stable for up to one year. As with all antibodies care should be taken to avoid repeated freeze thaw cycles. Antibodies should not be exposed to prolonged high temperatures.
  • 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

    227 kDa

    基因ID

    4627

    UniProt

    P35579

    途径

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