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Claudin 4 抗体

CLDN4 适用: 人, 小鼠 WB, ELISA, IHC 宿主: 兔 Polyclonal unconjugated
产品编号 ABIN7238078
发货至: 中国
  • 抗原 See all Claudin 4 (CLDN4) 抗体
    Claudin 4 (CLDN4)
    适用
    • 67
    • 29
    • 24
    • 8
    • 6
    • 5
    • 4
    • 2
    • 2
    • 1
    • 1
    人, 小鼠
    宿主
    • 59
    • 10
    克隆类型
    • 60
    • 9
    多克隆
    标记
    • 33
    • 4
    • 3
    • 3
    • 3
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
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    • 1
    This Claudin 4 antibody is un-conjugated
    应用范围
    • 55
    • 33
    • 13
    • 13
    • 12
    • 9
    • 4
    • 4
    • 3
    • 3
    • 2
    • 1
    Western Blotting (WB), ELISA, Immunohistochemistry (IHC)
    产品特性
    Polyclonal Antibody
    纯化方法
    Affinity purification
    免疫原
    Synthetic peptide of human CLDN4
    亚型
    IgG
    Top Product
    Discover our top product CLDN4 Primary Antibody
  • 应用备注
    WB 1:500-1:2000, IHC 1:25-1:100
    限制
    仅限研究用
  • 状态
    Liquid
    浓度
    0.3 mg/mL
    缓冲液
    PBS with 0.05 % sodium azide and 50 % glycerol, PH7.4
    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 4 (CLDN4)
    别名
    Claudin 4 (CLDN4 产品)
    别名
    CPE-R antibody, CPER antibody, CPETR antibody, CPETR1 antibody, WBSCR8 antibody, hCPE-R antibody, Cep-r antibody, Cpetr antibody, Cpetr1 antibody, CLDN4 antibody, cper antibody, cpe-r antibody, cpetr antibody, cpetr1 antibody, hcpe-r antibody, wbscr8 antibody, claudin 4 antibody, claudin 4 L homeolog antibody, CLDN4 antibody, Cldn4 antibody, cldn4 antibody, cldn4.L antibody
    背景
    Claudin 4, also known as CLDN4, is a protein which in humans is encoded by the CLDN4 gene. It belongs to the group of claudins. This gene encodes an integral membrane protein, which belongs to the claudin family. The protein is a component of tight junction strands and may play a role in internal organ development and function during pre- and postnatal life. This gene is deleted in Williams-Beuren syndrome, a neurodevelopmental disorder affecting multiple systems.
    分子量
    22 kDa
    NCBI登录号
    NP_001296
    UniProt
    O14493
    途径
    Hepatitis C
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