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Recombinant PVRL4 抗体

The Human Chimeric anti-PVRL4 antibody is suitable to detect PVRL4 in samples from 人. It has been validated for FACS.
产品编号 ABIN7490714
发货至: 中国
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北京 101111
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Room 801-803
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Tel +86 (0512) 65829739 传真 +86 (010) 6788 5057

Quick Overview for Recombinant PVRL4 抗体 (ABIN7490714)

抗原

See all PVRL4 抗体
PVRL4 (Poliovirus Receptor-Related 4 (PVRL4))

抗体类型

Recombinant Antibody

片段

Fc fragment

适用

  • 75
  • 24
  • 14

宿主

  • 48
  • 18
  • 12
  • 2
Human, 兔

克隆类型

  • 49
  • 29
  • 1
Chimeric

标记

  • 38
  • 6
  • 4
  • 4
  • 4
  • 3
  • 3
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
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  • 1
This PVRL4 antibody is un-conjugated

应用范围

  • 46
  • 29
  • 9
  • 4
  • 3
  • 3
  • 3
  • 1
Flow Cytometry (FACS)

克隆位点

DMC438
  • 原理

    Anti-Nectin4 antibody(DMC438), IgG1 Chimeric mAb

    纯化方法

    Purified from cell culture supernatant by affinity chromatography

    亚型

    IgG1
  • 应用备注

    Flow Cyt 1:100

    限制

    仅限研究用
  • 状态

    Lyophilized

    溶解方式

    Please see Certificate of Analysis for specific instructions of reconstitution.

    缓冲液

    Lyophilized from sterile PBS, pH 7.4. Normally 5 % - 8 % trehalose is added as protectants before lyophilization.

    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

    Nectin-4

    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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