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Claudin 11 抗体

CLDN11 适用: 人 IF 宿主: 兔 Polyclonal unconjugated
产品编号 ABIN7260581
发货至: 中国
  • 抗原 See all Claudin 11 (CLDN11) 抗体
    Claudin 11 (CLDN11)
    适用
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    宿主
    • 36
    克隆类型
    • 35
    • 1
    多克隆
    标记
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    This Claudin 11 antibody is un-conjugated
    应用范围
    • 31
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    Immunofluorescence (IF)
    产品特性
    Polyclonal Antibody
    纯化方法
    Affinity purification
    免疫原
    Recombinant fusion protein of human CLDN11 (NP_005593.2).
    亚型
    IgG
    Top Product
    Discover our top product CLDN11 Primary Antibody
  • 应用备注
    IF 1:20-1:50
    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
    Claudin 11 (CLDN11)
    别名
    CLDN11 (CLDN11 产品)
    别名
    cldn11 antibody, fb97c11 antibody, wu:fb97c11 antibody, claudin-11 antibody, CLDN11 antibody, Claudin-11 antibody, DKFZp459H2322 antibody, OSP antibody, OTM antibody, Claudin11 antibody, Osp antibody, Otm antibody, claudin 11b antibody, claudin 11 antibody, cldn11b antibody, CLDN11 antibody, Cldn11 antibody
    背景
    This gene encodes a member of the claudin family. Claudins are integral membrane proteins and components of tight junction strands. Tight junction strands serve as a physical barrier to prevent solutes and water from passing freely through the paracellular space between epithelial or endothelial cell sheets, and also play critical roles in maintaining cell polarity and signal transductions. The protein encoded by this gene is a major component of central nervous system (CNS) myelin and plays an important role in regulating proliferation and migration of oligodendrocytes. Mouse studies showed that the gene deficiency results in deafness and loss of the Sertoli cell epithelial phenotype in the testis. This protein is a tight junction protein at the human blood-testis barrier (BTB), and the BTB disruption is related to a dysfunction of this gene. Alternatively spliced transcript variants encoding different isoforms have been identified.
    基因ID
    5010
    UniProt
    O75508
    途径
    Hepatitis C
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