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Claudin 16 抗体 (N-Term)

This anti-Claudin 16 antibody is a 兔 多克隆 antibody detecting Claudin 16 in WB, FACS, IHC (p) 和 EIA. Suitable for 人.
产品编号 ABIN951545
发货至: 中国

Quick Overview for Claudin 16 抗体 (N-Term) (ABIN951545)

抗原

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

适用

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宿主

  • 39
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克隆类型

  • 40
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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), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p)), Enzyme Immunoassay (EIA)
  • 抗原表位

    • 15
    • 8
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    AA 13-41, N-Term

    特异性

    This antibody reacts to CLDN16.

    交叉反应 (详细)

    Species reactivity (tested):Human.

    纯化方法

    Affinity chromatography on Protein A

    免疫原

    KLH conjugated synthetic peptide between 13-41 amino acids from the N-terminal region of human CLDN16

    亚型

    Ig Fraction
  • 应用备注

    Optimal working dilution should be determined by the investigator.

    限制

    仅限研究用
  • 状态

    Liquid

    浓度

    0.25 mg/mL

    缓冲液

    PBS, 0.09 % (W/V) 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.

    注意事项

    Avoid repeated freezing and thawing.

    储存条件

    4 °C/-20 °C

    储存方法

    Store undiluted at 2-8 °C for one month or (in aliquots) at -20 °C for longer.
  • 抗原

    Claudin 16 (CLDN16)

    别名

    Claudin-16 / CLDN16

    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. 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.Synonyms: CL-16, PCLN-1, PCLN1, Paracellin-1

    分子量

    33836 Da

    基因ID

    10686

    NCBI登录号

    NP_006571

    途径

    Hepatitis C
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