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Lamin B Receptor 抗体

LBR 适用: 人, 小鼠, 大鼠 IHC, IF 宿主: 兔 Polyclonal unconjugated
产品编号 ABIN7261429
发货至: 中国
  • 抗原 See all Lamin B Receptor (LBR) 抗体
    Lamin B Receptor (LBR)
    适用
    • 27
    • 19
    • 3
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    人, 小鼠, 大鼠
    宿主
    • 25
    • 2
    克隆类型
    • 25
    • 2
    多克隆
    标记
    • 12
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
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    • 1
    This Lamin B Receptor antibody is un-conjugated
    应用范围
    • 27
    • 14
    • 6
    • 5
    • 5
    • 4
    • 3
    • 1
    Immunohistochemistry (IHC), Immunofluorescence (IF)
    产品特性
    Polyclonal Antibody
    纯化方法
    Affinity purification
    免疫原
    Recombinant fusion protein of human LBR (NP_002287.2).
    亚型
    IgG
    Top Product
    Discover our top product LBR Primary Antibody
  • 应用备注
    IHC 1:50-1:100 IF 1:50-1:100
    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
    Lamin B Receptor (LBR)
    别名
    LBR (LBR 产品)
    别名
    CG17952 antibody, Dmel\\CG17952 antibody, dLBR antibody, sb:cb406 antibody, zgc:86649 antibody, wu:fb75h08 antibody, wu:fc47b04 antibody, wu:fd36b07 antibody, lbr-A antibody, Xp58 antibody, p58 gene antibody, LBR antibody, DHCR14B antibody, LMN2R antibody, PHA antibody, TDRD18 antibody, AI505894 antibody, ic antibody, Nbp60 antibody, lamin B receptor antibody, Lamin B receptor antibody, lamin B receptor S homeolog antibody, LBR antibody, lbr antibody, lbr.S antibody, Lbr antibody
    背景
    The protein encoded by this gene belongs to the ERG4/ERG24 family. It localized in the nuclear envelope inner membrane and anchors the lamina and the heterochromatin to the membrane. It may mediate interaction between chromatin and lamin B. Mutations of this gene has been associated with autosomal recessive HEM/Greenberg skeletal dysplasia. Alternative splicing occurs at this locus and two transcript variants encoding the same protein have been identified.
    基因ID
    3930
    UniProt
    Q14739
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