北京索莱宝科技有限公司
产品展厅
Anti-MYH9 Polyclonal Antibody / 100μl
  • 品牌:solarbio
  • 产地:北京
  • 货号:K001583P
  • 发布日期: 2018-07-10
  • 更新日期: 2025-08-01
产品详请
产地 北京
品牌 solarbio
保存条件 Store at -20°C. Avoid freeze / thaw cycles.Stable for one year from the date of shipment.
货号 K001583P
应用范围 WB
CAS编号
抗体名 Anti-MYH9 Polyclonal Antibody
克隆性
靶点 1支/100μl/1600RMB
适应物种 Human Mouse
形态 Lyophilized or Liquid
宿主 Mouse
亚型 IgG
标识物
浓度 %
免疫原 Recombinant protein of human MYH9
英文名称Rabbit MYH9 Polyclonal Antibody
别名BDPLT6;DFNA17;EPSTS;FTNS;MHA;NMHC-II-A;NMMHC-IIA;NMMHCA 
应用WB,IHC
稀释比例WB1:1000-1:2000 IHC1:50-1:100
交叉反应Human Mouse
蛋白分子量227kDa
Gene ID4627
保存Store at -20°C. Avoid freeze / thaw cycles.Stable for one year from the date of shipment.
储存液PBS with 0.02% sodium azide, 50% glycerol, pH7.3.
纯化方法Affinity purification
亚型IgG
免疫原Recombinant protein of human MYH9
性状Lyophilized or Liquid
Swiss ProtP35579
克隆类型Polyclonal Antibody
来源Rabbit
背景资料This gene encodes a conventional non-muscle myosin; this protein should not be confused with the unconventional myosin-9a or 9b (MYO9A or MYO9B). The encoded protein is a myosin IIA heavy chain that contains an IQ domain and a myosin head-like domain which is involved in several important functions, including cytokinesis, cell motility and maintenance of cell shape. Defects in this gene have been associated with non-syndromic sensorineural deafness autosomal dominant type 17, Epstein syndrome, Alport syndrome with macrothrombocytopenia, Sebastian syndrome, Fechtner syndrome and macrothrombocytopenia with progressive sensorineural deafness.


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