Myosin 9 抗体 (C-Term)
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Quick Overview for Myosin 9 抗体 (C-Term) (ABIN1536807)
抗原
See all Myosin 9 (MYH9) 抗体适用
宿主
克隆类型
标记
应用范围
克隆位点
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抗原表位
- AA 1840-1867, C-Term
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纯化方法
- This antibody is purified through a protein A column, followed by peptide affinity purification.
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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.
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亚型
- Ig Fraction
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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) antibodyKD Validated MYH9 适用: 人 WB, FACS, IF (p) 宿主: 小鼠 Monoclonal 24GB14220 unconjugated
anti-Myosin 9 (MYH9) antibodyKD Validated MYH9 适用: 人 WB, FACS, IF (p) 宿主: 小鼠 Monoclonal 24GB14225 unconjugated
anti-Myosin 9 (MYH9) (N-Term) antibodyKO Validated MYH9 适用: 人 WB, IP, IF, 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 1740-1960) antibodyMYH9 适用: 人 WB, IHC, IP, ICC 宿主: 兔 Polyclonal 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 134-165), (N-Term) antibodyMYH9 适用: 人, 小鼠 WB, FACS 宿主: 兔 Polyclonal RB36361 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: 1:2000. WB: 1:2000
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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
- Purified polyclonal antibody supplied in PBS with 0.09 % (W/V) sodium azide.
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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
- 4 °C,-20 °C
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储存方法
- MYH9 Antibody (C-term) can be refrigerated at 2-8 °C for up to 6 months. For long term storage, keep at -20 °C.
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有效期
- 6 months
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- Myosin 9 (MYH9)
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别名
- MYH9
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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.
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分子量
- 226532
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基因ID
- 4627
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NCBI登录号
- NP_002464
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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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