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NDRG1 抗体

The 兔 多克隆 anti-NDRG1 antibody is suitable to detect NDRG1 in samples from 人 和 犬. It has been validated for WB 和 ELISA.
产品编号 ABIN2463116
发货至: 中国
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中国
北京 101111
No. 88 KeChuang 6th Street
Beijing Economic Technological Development Area
Room 801-803
4A Biotech Co.,Ltd.
Tel +86 (0512) 65829739 传真 +86 (010) 6788 5057

Quick Overview for NDRG1 抗体 (ABIN2463116)

抗原

See all NDRG1 抗体
NDRG1 (N-Myc Downstream Regulated 1 (NDRG1))

适用

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人, 犬

宿主

  • 93
  • 8
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克隆类型

  • 71
  • 32
多克隆

标记

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  • 1
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This NDRG1 antibody is un-conjugated

应用范围

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Western Blotting (WB), ELISA
  • 纯化方法

    Antibody is purified by protein A chromatography method.

    免疫原

    Antibody produced in rabbits immunized with a synthetic peptide corresponding a region of human NDRG1.
  • 应用备注

    NDRG1 antibody can be used for detection of NDRG1 by ELISA at 1:62500. NDRG1 antibody can be used for detection of NDRG1 by western blot at 2.5 μg/mL, and HRP conjugated secondary antibody should be diluted 1:50,000 - 100,000.

    限制

    仅限研究用
  • 状态

    Lyophilized

    溶解方式

    Add 100 ?L of distilled water. Final antibody concentration is 1 mg/mL.

    浓度

    1 mg/mL

    缓冲液

    Antibody is lyophilized in PBS buffer with 2 % sucrose.

    注意事项

    As with any antibody avoid repeat freeze-thaw cycles.

    储存条件

    4 °C/-20 °C

    储存方法

    For short periods of storage (days) store at 4 °C. For longer periods of storage, store NDRG1 antibody at -20 °C.
  • 抗原

    NDRG1 (N-Myc Downstream Regulated 1 (NDRG1))

    别名

    NDRG1

    背景

    NDRG1 is a member of the N-myc downregulated protein family which belongs to the alpha/beta hydrolase superfamily. NDRG1 is a cytoplasmic protein involved in stress responses, hormone responses, cell growth, and differentiation. Mutation in its gene has been reported to be causative for hereditary motor and sensory neuropathy-Lom.This gene is a member of the N-myc downregulated gene family which belongs to the alpha/beta hydrolase superfamily. The protein encoded by this gene is a cytoplasmic protein involved in stress responses, hormone responses, cell growth, and differentiation. Mutation in this gene has been reported to be causative for hereditary motor and sensory neuropathy-Lom.

    分子量

    43 kDa

    基因ID

    10397

    NCBI登录号

    NP_006087

    UniProt

    Q92597
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