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NEUROD1 抗体 (AA 15-45)

This anti-NEUROD1 antibody is a 兔 多克隆 antibody detecting NEUROD1 in WB, ELISA, IHC 和 IF. Suitable for 人.
产品编号 ABIN3031977
发货至: 中国

Quick Overview for NEUROD1 抗体 (AA 15-45) (ABIN3031977)

抗原

See all NEUROD1 抗体
NEUROD1 (Neuronal Differentiation 1 (NEUROD1))

适用

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宿主

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克隆类型

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多克隆

标记

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This NEUROD1 antibody is un-conjugated

应用范围

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Western Blotting (WB), ELISA, Immunohistochemistry (IHC), Immunofluorescence (IF)
  • 抗原表位

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    AA 15-45

    纯化方法

    Purified

    免疫原

    A portion of amino acids 15-45 from the human protein was used as the immunogen for this NeuroD1 antibody.

    亚型

    Ig Fraction
  • 应用备注

    Titration of the NeuroD1 antibody may be required due to differences in protocols and secondary/substrate sensitivity.\. Western blot: 1:1000,Immunofluorescence: 1:10-1:50,IHC (Paraffin): 1:50-1:100

    限制

    仅限研究用
  • 状态

    Liquid

    缓冲液

    In 1X PBS, pH 7.4, with 0.09 % 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

    Aliquot the NeuroD1 antibody and store frozen at -20°C or colder. Avoid repeated freeze-thaw cycles.
  • 抗原

    NEUROD1 (Neuronal Differentiation 1 (NEUROD1))

    别名

    NeuroD1

    背景

    NeuroD1 acts as a differentiation factor during neurogenesis. They are expressed transiently in a subset of neurons in the central and peripheral nervous systems at the time of their terminal differentiation. NeuroD1 is a basic helix-loop-helix (bHLH) protein contain 1 bHLH domain. NeuroD1 is a transcriptional activator, for efficient DNA binding it requires dimerization with another bHLH protein. It was reported that NeuroD1 involves heterodimerization with the ubiquitous bHLH protein E47, and regulates insulin gene expression by binding to a critical E-box motif on the insulin promoter. Defects in NEUROD1 causes maturity onset diabetes of the young type VI. MODY6 is a form of non-insulin-dependent diabetes mellitus (NIDDM) characterized by an autosomal dominant mode of inheritance, onset during young adulthood and a primary defect in insulin secretion.

    UniProt

    Q13562

    途径

    Dopaminergic Neurogenesis, Hormone Transport, Carbohydrate Homeostasis
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