×
我们推荐在您的浏览器上开启Javascript,以获得最佳效果。
Emerin 抗体 (C-Term)
EMD
适用: 人
WB, FACS
宿主: 兔
Polyclonal
RB19617
unconjugated
Emerin抗体详情
(hide)
抗原
See all Emerin (EMD) 抗体
Emerin (EMD)
抗原表位
All epitopes for Emerin 抗体
AA 187-213, C-Term
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), Flow Cytometry (FACS)
纯化方法
This antibody is prepared by Saturated Ammonium Sulfate (SAS) precipitation followed by dialysis against PBS.
免疫原
This EMD antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 187-213 amino acids from the C-terminal region of human EMD.
克隆位点
RB19617
亚型
Ig Fraction
Top Product
Discover our top product EMD Primary Antibody
Alternatives
(show)
使用细节
(hide)
应用备注
WB: 1:1000. FC: 1:10~50
限制
仅限研究用
贮存及处理
(hide)
状态
Liquid
缓冲液
Purified polyclonal antibody supplied in PBS with 0.09 % (W/V) sodium azide.
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
4 °C,-20 °C
储存方法
Maintain refrigerated at 2-8 °C for up to 6 months. For long term storage store at -20 °C in small aliquots to prevent freeze-thaw cycles.
有效期
6 months
Emerin目标详情
(hide)
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.
分子量
28994
基因ID
2010
NCBI登录号
NP_000108
UniProt
P50402
Recently viewed
(hide)