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Myosin VI 抗体

MYO6 适用: 人, 小鼠, 大鼠 WB, IF 宿主: 兔 Polyclonal unconjugated
产品编号 ABIN7256548
发货至: 中国
  • 抗原 See all Myosin VI (MYO6) 抗体
    Myosin VI (MYO6)
    适用
    • 29
    • 25
    • 25
    • 1
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    人, 小鼠, 大鼠
    宿主
    • 43
    • 1
    克隆类型
    • 43
    • 1
    多克隆
    标记
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    This Myosin VI antibody is un-conjugated
    应用范围
    • 22
    • 20
    • 16
    • 13
    • 13
    • 13
    • 8
    • 6
    • 3
    • 1
    • 1
    Western Blotting (WB), Immunofluorescence (IF)
    产品特性
    Polyclonal Antibody
    纯化方法
    Affinity purification
    免疫原
    Recombinant fusion protein of human MYO6 (NP_004990.3).
    亚型
    IgG
    Top Product
    Discover our top product MYO6 Primary Antibody
  • 应用备注
    WB 1:500-1:2000 IF 1:50-1:200
    限制
    仅限研究用
  • 状态
    Liquid
    浓度
    1 mg/mL
    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.
  • 抗原
    Myosin VI (MYO6)
    别名
    MYO6 (MYO6 产品)
    别名
    95F antibody, 95F MHC antibody, CG5695 antibody, Dm 95F antibody, Dm95F antibody, Dmel\\CG5695 antibody, Dro95F antibody, JAG antibody, Jaguar antibody, Jar antibody, M6 antibody, MHC95F antibody, MYOVI antibody, Mhc95F antibody, MyoVI antibody, Myosin VI antibody, jag antibody, ms(3)06746 antibody, myosins VI antibody, DFNA22 antibody, DFNB37 antibody, BC029719 antibody, Tlc antibody, sv antibody, RGD1560646 antibody, CMY6 antibody, jaguar antibody, myosin VI antibody, jar antibody, LOC373230 antibody, MYO6 antibody, myo6 antibody, Myo6 antibody
    背景
    This gene encodes a reverse-direction motor protein that moves toward the minus end of actin filaments and plays a role in intracellular vesicle and organelle transport. The protein consists of a motor domain containing an ATP- and an actin-binding site and a globular tail which interacts with other proteins. This protein maintains the structural integrity of inner ear hair cells and mutations in this gene cause non-syndromic autosomal dominant and recessive hearing loss. Alternative splicing results in multiple transcript variants encoding distinct isoforms.
    分子量

    Observed_MW: 150 kDa

    Calculated_MW: 145 kDa/146 kDa/148 kDa/149 kDa

    基因ID
    4646
    UniProt
    Q9UM54
    途径
    Sensory Perception of Sound, Dicarboxylic Acid Transport, Asymmetric Protein Localization
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