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Claudin 16 抗体

The 兔 多克隆 anti-Claudin 16 antibody is suitable to detect Claudin 16 in samples from 人, 小鼠 和 大鼠. It has been validated for WB, FACS 和 IF.
产品编号 ABIN7880445
发货至: 中国
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Quick Overview for Claudin 16 抗体 (ABIN7880445)

抗原

See all Claudin 16 (CLDN16) 抗体
Claudin 16 (CLDN16)

适用

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人, 小鼠, 大鼠

宿主

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克隆类型

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多克隆

标记

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This Claudin 16 antibody is un-conjugated

应用范围

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Western Blotting (WB), Flow Cytometry (FACS), Immunofluorescence (IF)
  • 原理

    Claudin 16 Antibody / CLDN16

    序列

    KSYSAPRTET AKMYAVDTRV

    纯化方法

    Affinity purified

    免疫原

    Amino acids KSYSAPRTETAKMYAVDTRV from the human protein were used as the immunogen for the Claudin 16 antibody.

    亚型

    IgG
  • 应用备注

    Optimal dilution of the Claudin 16 antibody should be determined by the researcher.

    限制

    仅限研究用
  • 状态

    Lyophilized

    缓冲液

    0.5 mg/mL if reconstituted with 0.2 mL sterile DI water

    储存条件

    4 °C,-20 °C

    储存方法

    After reconstitution, the Claudin 16 antibody can be stored for up to one month at 4oC. For long-term, aliquot and store at -20oC. Avoid repeated freezing and thawing.
  • 抗原

    Claudin 16 (CLDN16)

    别名

    Claudin 16

    背景

    Claudin-16 is a protein that in humans is encoded by the CLDN16 gene. 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. It is found primarily in the kidneys, specifically in the thick ascending limb of Henle, where it acts as either an intercellular pore or ion concentration sensor to regulate the paracellular resorption of magnesium ions. Defects in this gene are a cause of primary hypomagnesemia, which is characterized by massive renal magnesium wasting with hypomagnesemia and hypercalciuria, resulting in nephrocalcinosis and renal failure. This gene and the CLDN1 gene are clustered on chromosome 3q28.

    UniProt

    Q9Y5I7

    途径

    Hepatitis C
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