MYO5A 抗体 (C-Term)
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Quick Overview for MYO5A 抗体 (C-Term) (ABIN7467586)
抗原
See all MYO5A 抗体适用
宿主
克隆类型
标记
应用范围
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抗原表位
- C-Term
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交叉反应
- 人
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纯化方法
- Purified by antigen-affinity chromatography.
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免疫原
- Recombinant protein encompassing a sequence within the C-terminus region of human MYO5A. The exact sequence is proprietary.
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亚型
- IgG
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anti-Myosin VA (MYO5A) (AA 1087-1220) antibody
MYO5A 适用: 人 WB, ELISA, IHC, IF 宿主: 兔 Polyclonal unconjugated
anti-Myosin VA (MYO5A) antibodyMYO5A 适用: 人, 小鼠, 大鼠 WB, IHC 宿主: 兔 Polyclonal unconjugated
anti-Myosin VA (MYO5A) (AA 1531-1855) antibodyMYO5A 适用: 人 WB, IHC, IP, ICC 宿主: 兔 Polyclonal unconjugated
anti-Myosin VA (MYO5A) (Internal Region) antibodyVerified MYO5A 适用: 人, 小鼠 WB, ELISA, IF 宿主: 山羊 Polyclonal unconjugated
anti-Myosin VA (MYO5A) (AA 950-1150) antibodyMYO5A 适用: 人 WB, IF 宿主: 兔 Polyclonal unconjugated
anti-Myosin VA (MYO5A) (C-Term) antibodyMYO5A 适用: 人 WB, ELISA 宿主: 兔 Polyclonal unconjugated
anti-Myosin VA (MYO5A) (C-Term) antibodyMYO5A 适用: 人, 小鼠, 大鼠 WB, ELISA, IF, ICC 宿主: 兔 Polyclonal unconjugated
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应用备注
- WB: 1:500-1:3000. 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: U87-MG , SK-N-SH
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限制
- 仅限研究用
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状态
- Liquid
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浓度
- 0.84 mg/mL
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缓冲液
- 1XPBS ( pH 7), 20 % Glycerol, 0.025 % ProClin 300
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储存液
- ProClin
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注意事项
- This product contains ProClin: 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
- 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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- MYO5A (Myosin VA (MYO5A))
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别名
- myosin VA
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背景
- Myosin VA , GS1 , MYH12 , MYO5 , MYR12,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. [provided by RefSeq]
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分子量
- 215 kDa
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基因ID
- 4644
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UniProt
- Q9Y4I1
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途径
- Hormone Transport, Peptide Hormone Metabolism
抗原
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