MYH9 monoclonal antibody (M04), clone 4D1-抗体-抗体-生物在线
亚诺法生技股份有限公司（Abnova)
MYH9 monoclonal antibody (M04), clone 4D1

MYH9 monoclonal antibody (M04), clone 4D1

商家询价

产品名称： MYH9 monoclonal antibody (M04), clone 4D1

英文名称： MYH9 monoclonal antibody (M04), clone 4D1

产品编号： H00004627-M04

产品价格： null

产品产地： 台湾

品牌商标： Abnova

更新时间： null

使用范围：

亚诺法生技股份有限公司（Abnova)
  • 联系人 :
  • 地址 : 台湾台北市内湖区洲子街 108 号 9 楼
  • 邮编 : 11493
  • 所在区域 : 台湾
  • 电话 : +886-920**1152 点击查看
  • 传真 : 点击查看
  • 邮箱 : sales@abnova.com.tw
进入展台

  • Specification
  • Product Description:
  • Mouse monoclonal antibody raised against a partial recombinant MYH9.
  • Immunogen:
  • MYH9 (AAH11915, 131 a.a. ~ 220 a.a) partial recombinant protein with GST tag. MW of the GST tag alone is 26 KDa.
  • Sequence:
  • RLKQLKRQLEEAEEEAQRANASRRKLQRELEDATETADAMNREVSSLKNKLRRGDLPFVVPRRMARKGAGDGSDEEVDGKADGAEAKPAE
  • Host:
  • Mouse
  • Reactivity:
  • Human
  • Isotype:
  • IgG3 Kappa
  • Storage Buffer:
  • In 1x PBS, pH 7.2
  • Storage Instruction:
  • Store at -20°C or lower. Aliquot to avoid repeated freezing and thawing.
  • Quality Control Testing:
  • Antibody Reactive Against Recombinant Protein.

    QC Testing of H00004627-M04
    Western Blot detection against Immunogen (35.64 KDa) .
  • Applications
  • Sandwich ELISA (Recombinant protein)
  • Sandwich ELISA (Recombinant protein)
  • Detection limit for recombinant GST tagged MYH9 is approximately 0.3ng/ml as a capture antibody.
  • Protocol Download
  • ELISA
  • Application Image
  • Western Blot (Recombinant protein)
  • Sandwich ELISA (Recombinant protein)
  • Sandwich ELISA (Recombinant protein)
  • enlarge
  • ELISA
  • Gene Information
  • Entrez GeneID:
  • 4627
  • Gene Name:
  • MYH9
  • Gene Alias:
  • DFNA17,EPSTS,FTNS,MGC104539,MHA,NMHC-II-A,NMMHCA
  • Gene Description:
  • myosin, heavy chain 9, non-muscle
  • Gene Summary:
  • 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. [provided by RefSeq
  • Other Designations:
  • MYH9 variant protein,OTTHUMP00000028706,cellular myosin heavy chain, type A,myosin, heavy polypeptide 9, non-muscle,non-muscle myosin heavy chain,non-muscle myosin heavy polypeptide 9,nonmuscle myosin heavy chain II-A

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