Myosin 9 (MYH9) (Middle Region) Peptide
MYH9
适用: 人
宿主: 合成
BP, WB
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- 抗原 See all Myosin 9 (MYH9) products
- Myosin 9 (MYH9)
- 蛋白结构域
- Middle Region
- 宿主
- 人
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资源
- 合成
- 应用范围
- Blocking Peptide (BP), Western Blotting (WB)
- 产品特性
- This is a synthetic peptide designed for use in combination with anti-MYH9 antibody (Catalog #: ARP48072_P050). It may block above mentioned antibody from binding to its target protein in western blot and/or immunohistochecmistry under proper experimental settings. There is no guarantee for its use in other applications.
- 纯化方法
- Purified
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- 应用备注
- Each Investigator should determine their own optimal working dilution for specific applications.
- 限制
- 仅限研究用
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- 状态
- Lyophilized
- 溶解方式
- Add 100 μL of sterile PBS. Final peptide concentration is 1 mg/mL in PBS.
- 浓度
- 1 mg/mL
- 缓冲液
- Final peptide concentration is 1 mg/mL in PBS.
- 注意事项
- Avoid repeated freeze-thaw cycles.
- 储存条件
- -20 °C
- 储存方法
- For longer periods of storage, store at -20°C. Avoid repeat freeze-thaw cycles.
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- 抗原
- Myosin 9 (MYH9)
- 别名
- BDPLT6 Peptide, DFNA17 Peptide, EPSTS Peptide, FTNS Peptide, MHA Peptide, NMHC-II-A Peptide, NMMHC-IIA Peptide, NMMHCA Peptide, C80049 Peptide, D0Jmb2 Peptide, E030044M24Rik Peptide, Fltn Peptide, Myhn-1 Peptide, Myhn1 Peptide, NMHC II-A Peptide, NMHCIIA Peptide, NMMHC II-a Peptide, NMMHC-A Peptide, TU72.6 Peptide, fi22c04 Peptide, myh9 Peptide, myh9l2 Peptide, wu:fi22c04 Peptide, wu:fj85e11 Peptide, zgc:162029 Peptide, zgc:66164 Peptide, NMMHC Peptide, myosin Peptide, non-muscle Peptide, nonmuscle Peptide, KLG/PTK7 Peptide, dfna17 Peptide, epsts Peptide, ftns Peptide, nmhc-ii-a Peptide, nmmhca Peptide, myosin heavy chain 9 Peptide, myosin, heavy polypeptide 9, non-muscle Peptide, myosin, heavy chain 9a, non-muscle Peptide, myosin, heavy chain 9, non-muscle Peptide, myosin, heavy chain 9, non-muscle L homeolog Peptide, MYH9 Peptide, Myh9 Peptide, myh9a Peptide, myh9.L Peptide
- 背景
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MYH9 is 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.
Alias Symbols: DFNA17, EPSTS, FTNS, MGC104539, MHA, NMHC-II-A, NMMHCA, BDPLT6, NMMHC-IIA
Protein Interaction Partner: ASCC2,CD163,CXCR4,GRIN1,MEN1,MYBPC3,MYH10,MYL9,MYOM1,MYOM2,OVGP1,PTPN6,S100A4,TTN,TUFM,ASCC2,EPB41,MARK4,MYL9,PRKCE,USP1,USP45
Protein Size: 1960 - 分子量
- 226 kDa
- 基因ID
- 4627
- NCBI登录号
- NM_002473, NP_002464
- UniProt
- P35579
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