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MNX1 抗体 (AA 260-340)

This 兔 多克隆 anti-MNX1 antibody specifically detects MNX1 in WB 和 ELISA. The antibody is reactive with 人 和 小鼠 samples.
产品编号 ABIN7229710
发货至: 中国
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Quick Overview for MNX1 抗体 (AA 260-340) (ABIN7229710)

抗原

See all MNX1 抗体
MNX1 (Motor Neuron and Pancreas Homeobox 1 (MNX1))

适用

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人, 小鼠

宿主

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克隆类型

  • 58
  • 13
多克隆

标记

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This MNX1 antibody is un-conjugated

应用范围

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Western Blotting (WB), ELISA
  • 抗原表位

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    AA 260-340

    原理

    MNX1 Polyclonal Antibody

    特异性

    The antibody detects endogenous levels of MNX1 protein

    纯化方法

    The antibody was affinity-purified from rabbit serum by affinity-chromatography using specific immunogen

    免疫原

    Synthesized peptide derived from part region of human MNX1 protein at AA range: 260-340

    亚型

    IgG
  • 应用备注

    Optimal working dilutions should be determined experimentally by the investigator. Suggested starting dilutions are as follows: WB (1:500-1:2000), ELISA (1:5000-1:20000).

    说明

    Primary Antibody

    限制

    仅限研究用
  • 状态

    Liquid

    浓度

    1 mg/mL

    缓冲液

    PBS, pH 7.4, containing 0.02 % Sodium Azide as preservative and 50 % Glycerol.

    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

    Stable for one year at -20°C from date of shipment. For maximum recovery of product, centrifuge the original vial after thawing and prior to removing the cap. Aliquot to avoid repeated freezing and thawing.
  • 抗原

    MNX1 (Motor Neuron and Pancreas Homeobox 1 (MNX1))

    别名

    MNX1

    背景

    Rabbit Anti-MNX1 Polyclonal Antibody,Motor neuron and pancreas homeobox protein 1, Homeobox protein HB9,MNX1 (Motor Neuron And Pancreas Homeobox 1) is a Protein Coding gene. Diseases associated with MNX1 include Currarino Syndrome and Meningocele. Among its related pathways are Regulation of beta-cell development and Neural Stem Cell Differentiation Pathways and Lineage-specific Markers. MNX1 encodes a nuclear protein, which contains a homeobox domain and is a transcription factor. Mutations in MNX1 result in Currarino syndrome, an autosomic dominant congenital malformation. Alternatively spliced transcript variants encoding different isoforms have been found for MNX1.,MNX1

    分子量

    observerd band 44kDa

    基因ID

    3110

    UniProt

    P50219
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