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DLX3 抗体

This anti-DLX3 antibody is a 兔 单克隆 antibody detecting DLX3 in WB. Suitable for 人.
产品编号 ABIN7266800
发货至: 中国

Quick Overview for DLX3 抗体 (ABIN7266800)

抗原

See all DLX3 抗体
DLX3 (Distal-Less Homeobox 3 (DLX3))

适用

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宿主

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克隆类型

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单克隆

标记

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This DLX3 antibody is un-conjugated

应用范围

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Western Blotting (WB)
  • 原理

    DLX3 Rabbit mAb

    交叉反应

    人, 小鼠

    产品特性

    Monoclonal Antibodies

    纯化方法

    Affinity purification

    免疫原

    Recombinant protein of Human DLX3.

    亚型

    IgG
  • 应用备注

    WB,1:500 - 1:2000

    限制

    仅限研究用
  • 状态

    Liquid

    缓冲液

    PBS with 0.02 % sodium azide,0.05 % BSA,50 % glycerol, pH 7.3.

    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

    Store at -20°C. Avoid freeze / thaw cycles.
  • 抗原

    DLX3 (Distal-Less Homeobox 3 (DLX3))

    别名

    DLX3

    背景

    Many vertebrate homeo box-containing genes have been identified on the basis of their sequence similarity with Drosophila developmental genes. Members of the Dlx gene family contain a homeobox that is related to that of Distal-less (Dll), a gene expressed in the head and limbs of the developing fruit fly. The Distal-less (Dlx) family of genes comprises at least 6 different members, DLX1-DLX6. Trichodentoosseous syndrome (TDO), an autosomal dominant condition, has been correlated with DLX3 gene mutation. This gene is located in a tail-to-tail configuration with another member of the gene family on the long arm of chromosome 17. Mutations in this gene have been associated with the autosomal dominant conditions trichodentoosseous syndrome and amelogenesis imperfecta with taurodontism.,DLX3,AI4,TDO,Epigenetics & Nuclear Signaling,Transcription Factors,DLX3

    分子量

    31kDa

    基因ID

    1747

    UniProt

    O60479
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