MYO5A 抗体 (AA 950-1150)
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- 抗原 See all MYO5A 抗体
- MYO5A (Myosin VA (MYO5A))
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抗原表位
- AA 950-1150
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适用
- 人
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宿主
- 兔
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克隆类型
- 多克隆
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标记
- This MYO5A antibody is un-conjugated
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应用范围
- Western Blotting (WB), Immunofluorescence (IF)
- 序列
- LTNLEGIYNS ETEKLRSDLE RLQLSEEEAK VATGRVLSLQ EEIAKLRKDL EQTRSEKKCI EEHADRYKQE TEQLVSNLKE ENTLLKQEKE ALNHRIVQQA KEMTETMEKK LVEETKQLEL DLNDERLRYQ NLLNEFSRLE ERYDDLKEEM TLMVHVPKPG HKRTDSTHSS NESEYIFSSE IAEMEDIPSR TEEPSEKKVP L
- 交叉反应
- 人, 小鼠, 大鼠
- 产品特性
- Polyclonal Antibodies
- 免疫原
- Recombinant fusion protein containing a sequence corresponding to amino acids 950-1150 of human MYO5A (NP_000250.3).
- 亚型
- IgG
- Top Product
- Discover our top product MYO5A Primary Antibody
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- 应用备注
- WB,1:500 - 1:2000,IF,1:50 - 1:100
- 说明
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HIGH QUALITY
- 限制
- 仅限研究用
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- 状态
- Liquid
- 缓冲液
- PBS with 0.02 % sodium azide,50 % glycerol, pH 7.3.
- 储存液
- Sodium azide
- 注意事项
- This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
- 储存条件
- -20 °C
- 储存方法
- Store at -20°C. Avoid freeze / thaw cycles.
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- 抗原
- MYO5A (Myosin VA (MYO5A))
- 别名
- MYO5A (MYO5A 产品)
- 别名
- myo5a antibody, MGC53270 antibody, si:dkey-266j9.1 antibody, MYOA antibody, MYO5A antibody, D antibody, Dop antibody, Myh12 antibody, 9630007J19Rik antibody, AI413174 antibody, AI661011 antibody, Dbv antibody, MVa antibody, Myo5 antibody, MyoVA antibody, Sev-1 antibody, d antibody, d-120J antibody, flail antibody, flr antibody, DILUTE antibody, myoxin) antibody, non-muscle antibody, GS1 antibody, MYH12 antibody, MYO5 antibody, MYR12 antibody, myosin VA L homeolog antibody, myosin VAa antibody, myosin VA antibody, myosin va antibody, myo5a.L antibody, myo5aa antibody, MYO5A antibody, PY04789 antibody, Myo5a antibody
- 背景
- This gene is one of three myosin V heavy-chain genes, belonging to the myosin gene superfamily. Myosin V is a class of actin-based motor proteins involved in cytoplasmic vesicle transport and anchorage, spindle-pole alignment and mRNA translocation. The protein encoded by this gene is abundant in melanocytes and nerve cells. Mutations in this gene cause Griscelli syndrome type-1 (GS1), Griscelli syndrome type-3 (GS3) and neuroectodermal melanolysosomal disease, or Elejalde disease. Multiple alternatively spliced transcript variants encoding different isoforms have been reported, but the full-length nature of some variants has not been determined.,MYO5A,GS1,MYH12,MYO5,MYR12,myosin VA,Signal Transduction,Cell Biology & Developmental Biology,Cytoskeleton,Motor Proteins,Endocrine & Metabolism,Mitochondrial metabolism,Neuroscience,MYO5A
- 分子量
- 212 kDa/215 kDa/218 kDa
- 基因ID
- 4644
- UniProt
- Q9Y4I1
- 途径
- Hormone Transport, Peptide Hormone Metabolism
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