anti-MYO5A antibody

Key features and details

  • 产品描述: Goat Polyclonal antibody recognizes MYO5A
  • 反应物种: Hu, Ms
  • 预测物种: Cow, Rat
  • 应用: ICC/IF, WB
  • 特异性: This antibody is expected to recognize both reported isoforms (NP_000250.3; NP_001135967.1).
  • 宿主: Goat
  • 克隆: Polyclonal
  • 同位型: IgG
  • 靶点名称: MYO5A
  • Brand:
CAT.NO. : ARG65296
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Product Details
概述
产品描述Goat Polyclonal antibody recognizes MYO5A
反应物种Hu, Ms
预测物种Cow, Rat
应用ICC/IF, WB
特异性This antibody is expected to recognize both reported isoforms (NP_000250.3; NP_001135967.1).
宿主Goat
克隆Polyclonal
同位型IgG
靶点名称MYO5A
抗原物种Human
抗原C-ETKQLELDLN
偶联标记Un-conjugated
別名GS1; MYH12; Unconventional myosin-Va; MYR12; Myosin-12; MYO5; Dilute myosin heavy chain, non-muscle; Myoxin; Myosin heavy chain 12
应用说明
应用建议
应用推荐稀释比
ICC/IF1 - 3 µg/ml
WB1 - 3 µg/ml
应用说明WB: Recommend incubate at RT for 1h.
* The dilutions indicate recommended starting dilutions and the optimal dilutions or concentrations should be determined by the scientist.
属性
形式Liquid
纯化Purified from goat serum by ammonium sulphate precipitation followed by antigen affinity chromatography using the immunizing peptide.
缓冲液Tris saline (pH 7.3), 0.02% Sodium azide and 0.5% BSA
抗菌剂0.02% Sodium azide
稳定剂0.5% BSA
浓度0.5 mg/ml
存放说明For continuous use, store undiluted antibody at 2-8°C for up to a week. For long-term storage, aliquot and store at -20°C or below. Storage in frost free freezers is not recommended. Avoid repeated freeze/thaw cycles. Suggest spin the vial prior to opening. The antibody solution should be gently mixed before use.
注意事项For laboratory research only, not for drug, diagnostic or other use.
生物信息
数据库连接

GeneID: 17918 Mouse MYO5A

GeneID: 4644 Human MYO5A

Swiss-port # Q99104 Mouse Unconventional myosin-Va

Swiss-port # Q9Y4I1 Human Unconventional myosin-Va

背景介绍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, Dec 2008]
研究领域Metabolism antibody; Neuroscience antibody; Signaling Transduction antibody
预测分子量215 kDa
检测图片 (1)
  • ARG65296 anti-MYO5A antibody WB image

    Western Blot: Jurkat lysate (35 µg protein in RIPA buffer) stained with ARG65296 anti-MYO5A antibody at 1 µg/ml dilution.

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