Myosin 9 抗体
Quick Overview for Myosin 9 抗体 (ABIN7116598)
抗原
See all Myosin 9 (MYH9) 抗体适用
宿主
克隆类型
标记
应用范围
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纯化方法
- Immunogen affinity purified
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纯度
- ≥95 % as determined by SDS-PAGE
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免疫原
- myosin, heavy chain 9, non-muscle
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亚型
- IgG
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anti-Myosin 9 (MYH9) (AA 131-220) antibody
MYH9 适用: 人 WB, ELISA, IF, IHC (p) 宿主: 小鼠 Monoclonal 4H3 unconjugated
anti-Myosin 9 (MYH9) (AA 1711-1960) antibodyMYH9 适用: 人 WB, IHC, IP 宿主: 兔 Polyclonal unconjugated
anti-Myosin 9 (MYH9) (N-Term) antibodyKO Validated MYH9 适用: 人 WB, IF, IP, IHC (p), ICC 宿主: 兔 Polyclonal unconjugated
anti-Myosin 9 (MYH9) antibodyMYH9 适用: 人 WB, IF, IHC (p), EIA 宿主: 小鼠 Monoclonal 2B3 unconjugated
anti-Myosin 9 (MYH9) (AA 2-241) antibodyMYH9 适用: 人 ELISA, IHC, IF 宿主: 兔 Polyclonal unconjugated
anti-Myosin 9 (MYH9) (AA 1740-1960) antibodyMYH9 适用: 人 WB, IHC, IP, ICC 宿主: 兔 Polyclonal unconjugated
anti-Myosin 9 (MYH9) (AA 134-165), (N-Term) antibodyMYH9 适用: 人, 小鼠 WB, FACS 宿主: 兔 Polyclonal RB36361 unconjugated
anti-Myosin 9 (MYH9) (AA 131-220) antibodyMYH9 适用: 人 WB, ELISA, IF 宿主: 小鼠 Monoclonal 4D1 unconjugated
anti-Myosin 9 (MYH9) (AA 131-220) antibodyMYH9 适用: 人 WB, ELISA, IF 宿主: 小鼠 Monoclonal 1H6 unconjugated
anti-Myosin 9 (MYH9) (Internal Region) antibodyVerified MYH9 适用: 人, 小鼠 WB, ELISA 宿主: 山羊 Polyclonal unconjugated
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应用备注
- WB: 1:1000 - 1:2000, IHC: 1:50 - 1:100
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限制
- 仅限研究用
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状态
- Liquid
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缓冲液
- PBS with 0.02 % sodium azide and 50 % glycerol pH 7.3 ,
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储存液
- Sodium azide
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注意事项
- This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
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储存条件
- -20 °C
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储存方法
- -20°C for 12 months (Avoid repeated freeze / thaw cycles.)
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有效期
- 12 months
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- Myosin 9 (MYH9)
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别名
- MYH9
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背景
- Synonyms:BDPLT6 Background: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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分子量
- 250 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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