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CLDN14 抗体

CLDN14 适用: 人 WB 宿主: 兔 Polyclonal unconjugated
产品编号 ABIN6290241
发货至: 中国
  • 抗原 See all CLDN14 抗体
    CLDN14 (Claudin 14 (CLDN14))
    适用
    • 35
    • 11
    • 2
    • 1
    宿主
    • 31
    • 3
    • 1
    克隆类型
    • 33
    • 2
    多克隆
    标记
    • 18
    • 3
    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    This CLDN14 antibody is un-conjugated
    应用范围
    • 26
    • 19
    • 4
    • 3
    • 2
    • 1
    • 1
    • 1
    Western Blotting (WB)
    纯化方法
    Affinity purification
    免疫原
    Recombinant protein of human CLDN14
    亚型
    IgG
    Top Product
    Discover our top product CLDN14 Primary Antibody
  • 应用备注
    WB 1:500 - 1:2000
    说明

    Liver, kidney, Also found in ear

    限制
    仅限研究用
  • 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 -20C. Avoid freeze / thaw cycles.
  • 抗原
    CLDN14 (Claudin 14 (CLDN14))
    别名
    CLDN14 (CLDN14 产品)
    别名
    claudin-14 antibody, CLDN14 antibody, DFNB29 antibody, AI851731 antibody, claudin 14 L homeolog antibody, claudin 14 antibody, cldn14.L antibody, CLDN14 antibody, Cldn14 antibody
    背景
    Tight junctions represent one mode of cell-to-cell adhesion in epithelial or endothelial cell sheets, forming continuous seals around cells and serving as a physical barrier to prevent solutes and water from passing freely through the paracellular space. These junctions are comprised of sets of continuous networking strands in the outwardly facing cytoplasmic leaflet, with complementary grooves in the inwardly facing extracytoplasmic leaflet. The protein encoded by this gene, a member of the claudin family, is an integral membrane protein and a component of tight junction strands. The encoded protein also binds specifically to the WW domain of Yes-associated protein. Defects in this gene are the cause of an autosomal recessive form of nonsyndromic sensorineural deafness. It is also reported that four synonymous variants in this gene are associated with kidney stones and reduced bone mineral density. Several transcript variants encoding the same protein have been found for this gene.
    分子量
    25.699 kDa
    基因ID
    23562
    UniProt
    O95500
    途径
    Cell-Cell Junction Organization, Hepatitis C
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