Myosin 9 抗体 (N-Term)
Quick Overview for Myosin 9 抗体 (N-Term) (ABIN7464342)
抗原
See all Myosin 9 (MYH9) 抗体适用
宿主
克隆类型
标记
应用范围
质量等级
克隆位点
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抗原表位
- N-Term
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交叉反应
- 人, 小鼠
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纯化方法
- Affinity purified by Protein A.
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免疫原
- Recombinant protein encompassing a sequence within the N-terminus region of human MYH9. The exact sequence is proprietary.
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亚型
- IgG2b
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应用备注
- WB: 1:500-1:3000. IHC-P: 1:100-1:1000. Optimal dilutions/concentrations should be determined by the researcher. Not tested in other applications.
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说明
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Positive Control: A431
Validation: KO/KD
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限制
- 仅限研究用
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状态
- Liquid
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浓度
- 1 mg/mL
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缓冲液
- 1XPBS pH 7, 20 % Glycerol, No Preservative
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储存液
- Without preservative
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储存条件
- 4 °C,-20 °C
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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.
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- Myosin 9 (MYH9)
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别名
- myosin heavy chain 9
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背景
- Myosin heavy chain 9 , BDPLT6 , DFNA17 , EPSTS , FTNS , MATINS , MHA , NMHC-II-A , NMMHC-IIA , NMMHCA,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]
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分子量
- 227 kDa
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基因ID
- 4627
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UniProt
- P35579
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途径
- Regulation of G-Protein Coupled Receptor Protein Signaling, Integrin Complex
抗原
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