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Emerin 抗体 (AA 1-220)
EMD
适用: 人
WB, IF, IHC
宿主: 兔
Polyclonal
unconjugated
Emerin抗体详情
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抗原
See all Emerin (EMD) 抗体
Emerin (EMD)
抗原表位
All epitopes for Emerin 抗体
AA 1-220
适用
All reactivities for Emerin 抗体
人
宿主
All hosts for Emerin 抗体
兔
克隆类型
All clonalities for Emerin 抗体
多克隆
标记
All conjugates for Emerin 抗体
This Emerin antibody is un-conjugated
应用范围
All applications for Emerin 抗体
Western Blotting (WB), Immunofluorescence (IF), Immunohistochemistry (IHC)
序列
MDNYADLSDT ELTTLLRRYN IPHGPVVGST RRLYEKKIFE YETQRRRLSP PSSSAASSYS FSDLNSTRGD ADMYDLPKKE DALLYQSKGY NDDYYEESYF TTRTYGEPES AGPSRAVRQS VTSFPDADAF HHQVHDDDLL SSSEEECKDR ERPMYGRDSA YQSITHYRPV SASRSSLDLS YYPTSSSTSF MSSSSSSSSW LTRRAIRPEN RAPGAGLGQD
交叉反应
人, 小鼠
产品特性
Polyclonal Antibodies
纯化方法
Affinity purification
免疫原
Recombinant fusion protein containing a sequence corresponding to amino acids 1-220 of human Emerin/Emerin/EMD (NP_000108.1).
亚型
IgG
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Alternatives
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使用细节
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应用备注
WB,1:500 - 1:2000,IHC,1:50 - 1:200,IF,1:20 - 1:100
限制
仅限研究用
贮存及处理
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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.
注意事项
Avoid freeze / thaw cycles
储存条件
-20 °C
储存方法
Store at -20°C. Avoid freeze / thaw cycles.
Emerin目标详情
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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.,EMD,EDMD,LEMD5,STA,emerin,Signal Transduction,Cell Biology & Developmental Biology,Cytoskeleton,Intermediate Filaments,EMD
分子量
28 kDa
基因ID
2010
UniProt
P50402
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