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PVRL4 抗体

PVRL4 适用: 人 FACS 宿主: 兔 Chimeric unconjugated Fc fragment
产品编号 ABIN7490714
发货至: 中国
  • 抗原 See all PVRL4 抗体
    PVRL4 (Poliovirus Receptor-Related 4 (PVRL4))
    片段
    Fc fragment
    适用
    • 48
    • 22
    • 14
    宿主
    • 43
    • 5
    • 2
    克隆类型
    • 45
    • 5
    Chimeric
    标记
    • 23
    • 4
    • 4
    • 4
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    This PVRL4 antibody is un-conjugated
    应用范围
    • 47
    • 28
    • 5
    • 3
    • 2
    • 2
    • 1
    • 1
    Flow Cytometry (FACS)
    产品特性
    Rabbit/Human Fc chimeric IgG1
    纯化方法
    Purified from cell culture supernatant by affinity chromatography
    亚型
    IgG1
    Top Product
    Discover our top product PVRL4 Primary Antibody
  • 应用备注
    Flow Cyt  1:100
    限制
    仅限研究用
  • 状态
    Liquid
    储存条件
    -20 °C,-80 °C
    储存方法
    Store at -20°C to -80°C for 12 months in lyophilized form. After reconstitution, if not intended for use within a month, aliquot and store at -80°C (Avoid repeated freezing and thawing). Lyophilized proteins are shipped at ambient temperature.
    有效期
    12 months
  • 抗原
    PVRL4 (Poliovirus Receptor-Related 4 (PVRL4))
    别名
    NECTIN4 (PVRL4 产品)
    别名
    PVRL4 antibody, si:ch211-155e24.1 antibody, 1200017F15Rik antibody, Prr4 antibody, RGD1559826 antibody, EDSS1 antibody, LNIR antibody, PRR4 antibody, nectin-4 antibody, nectin cell adhesion molecule 4 antibody, NECTIN4 antibody, nectin4 antibody, Nectin4 antibody
    背景
    EDSS1, LNIR, nectin-4, PRR4, PVRL4,
    Description: This gene encodes a member of the nectin family. The encoded protein contains two immunoglobulin-like (Ig-like) C2-type domains and one Ig-like V-type domain. It is involved in cell adhesion through trans-homophilic and -heterophilic interactions. It is a single-pass type I membrane protein. The soluble form is produced by proteolytic cleavage at the cell surface by the metalloproteinase ADAM17/TACE. The secreted form is found in both breast tumor cell lines and breast tumor patients. Mutations in this gene are the cause of ectodermal dysplasia-syndactyly syndrome type 1, an autosomal recessive disorder. Alternatively spliced transcript variants have been found but the full-length nature of the variant has not been determined.
    UniProt
    Q96NY8
    途径
    Cell-Cell Junction Organization
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