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Tricellulin 抗体 (AA 12-496) (PE)

This 兔 多克隆 antibody specifically detects Tricellulin in FACS. It exhibits reactivity toward 人 和 大鼠.
产品编号 ABIN8049491
发货至: 中国
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Quick Overview for Tricellulin 抗体 (AA 12-496) (PE) (ABIN8049491)

抗原

See all Tricellulin (MARVELD2) 抗体
Tricellulin (MARVELD2)

适用

  • 41
  • 22
  • 12
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
人, 大鼠

宿主

  • 41

克隆类型

  • 41
多克隆

标记

  • 19
  • 4
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This Tricellulin antibody is conjugated to PE

应用范围

  • 26
  • 17
  • 15
  • 10
  • 3
  • 2
  • 2
Flow Cytometry (FACS)
  • 抗原表位

    • 12
    • 8
    • 4
    • 3
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    AA 12-496

    原理

    Anti-MARVELD2 Antibody PE Conjugated

    预测反应

    Human MARVELD2 shares 87% amino acid (aa) sequence identity with mouse MARVELD2.

    纯化方法

    Immunogen affinity purified.

    免疫原

    E.coli-derived human MARVELD2 recombinant protein (Position: R12-H496). Human MARVELD2 shares 87% amino acid (aa) sequence identity with mouse MARVELD2.

    亚型

    IgG
  • 应用备注

    Flow Cytometry, Optimal dilutions should be determined by end users.

    限制

    仅限研究用
  • 状态

    Liquid

    缓冲液

    Each vial contains 50 % glycerol, 0.9 % NaCl, 0.2 % Na2HPO4, 0.02 % Sodium azide.

    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

    At -20°C for one year from date of receipt. Avoid repeated freezing and thawing. Protect from light.

    有效期

    12 months
  • 抗原

    Tricellulin (MARVELD2)

    别名

    MARVELD2

    背景

    Background: MARVEL domain-containing protein 2 is a protein that in humans is encoded by the MARVELD2 gene. The protein encoded by this gene is a membrane protein found at the tight junctions between epithelial cells. The encoded protein helps establish epithelial barriers such as those in the organ of Corti, where these barriers are required for normal hearing. Defects in this gene are a cause of deafness autosomal recessive type 49 (DFNB49). Two transcript variants encoding different isoforms have been found for this gene.

    Gene Full Name: MARVEL domain containing 2

    基因ID

    153562

    UniProt

    Q8N4S9

    途径

    Sensory Perception of Sound, Cell-Cell Junction Organization
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