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Emerin 抗体

EMD 适用: 人 WB, IF, IHC 宿主: 兔 Monoclonal unconjugated
产品编号 ABIN7266933
发货至: 中国
  • 抗原 See all Emerin (EMD) 抗体
    Emerin (EMD)
    适用
    • 58
    • 16
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    • 3
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    • 1
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    宿主
    • 46
    • 12
    • 2
    克隆类型
    • 48
    • 12
    单克隆
    标记
    • 34
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    • 1
    • 1
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    • 1
    • 1
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    • 1
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    This Emerin antibody is un-conjugated
    应用范围
    • 47
    • 14
    • 14
    • 13
    • 13
    • 9
    • 8
    • 8
    • 6
    • 5
    • 4
    • 2
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    Western Blotting (WB), Immunofluorescence (IF), Immunohistochemistry (IHC)
    原理
    Emerin/EMD Rabbit mAb
    交叉反应
    人, 小鼠, 大鼠
    产品特性
    Monoclonal Antibodies
    纯化方法
    Affinity purification
    免疫原
    A synthesized peptide derived from human Emerin/EMD
    亚型
    IgG
    Top Product
    Discover our top product EMD Primary Antibody
  • 应用备注
    WB,1:500 - 1:2000,IHC,1:50 - 1:200,IF,1:50 - 1:200
    限制
    仅限研究用
  • 状态
    Liquid
    缓冲液
    PBS with 0.02 % sodium azide,0.05 % BSA,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
    Emerin (EMD)
    别名
    EMD (EMD 产品)
    别名
    fj58f01 antibody, wu:fj58f01 antibody, EMD antibody, Bocks antibody, Bocksbeutel antibody, CG9424 antibody, Dmel\\CG9424 antibody, emerin antibody, emd antibody, xemd1 antibody, xemerin2 antibody, xemd2 antibody, xemerin1 antibody, EDMD antibody, LEMD5 antibody, STA antibody, AW550900 antibody, Sta antibody, emerin antibody, emerin (Emery-Dreifuss muscular dystrophy) antibody, bocksbeutel antibody, emerin L homeolog antibody, emerin S homeolog antibody, EMD antibody, emd antibody, bocks antibody, emd.L antibody, emd.S antibody, Emd antibody
    背景
    Emerin is a serine-rich nuclear membrane protein and a member of the nuclear lamina-associated protein family. It mediates membrane anchorage to the cytoskeleton. Dreifuss-Emery muscular dystrophy is an X-linked inherited degenerative myopathy resulting from mutation in the emerin gene. [provided by RefSeq, Jul 2008],EDMD, LEMD5, STA,Cell Biology & Developmental Biology,Cytoskeleton,Cytoskeleton_Intermediate Filaments,Signal Transduction,EMD
    分子量
    29kDa
    基因ID
    2010
    UniProt
    P50402
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