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FOXP2 抗体

This anti-FOXP2 antibody is a 小鼠 单克隆 antibody detecting FOXP2 in ELISA. Suitable for 人. This Primary Antibody has been cited in 2+ publications.
产品编号 ABIN969154
发货至: 中国

Quick Overview for FOXP2 抗体 (ABIN969154)

抗原

See all FOXP2 抗体
FOXP2 (Forkhead Box P2 (FOXP2))

适用

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宿主

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小鼠

克隆类型

  • 36
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  • 1
单克隆

标记

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This FOXP2 antibody is un-conjugated

应用范围

  • 32
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ELISA

克隆位点

5C11A8
  • 原理

    FOXP2 Antibody

    纯化方法

    Ascitic fluid

    免疫原

    Purified recombinant fragment of human MAPK3 expressed in E. Coli.

    亚型

    IgG1
  • 应用备注

    ELISA: 1/10000

    限制

    仅限研究用
  • 状态

    Liquid

    缓冲液

    Ascitic fluid containing 0.03 % 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

    4 °C,-20 °C

    储存方法

    Store at 4°C short term. Aliquot and store at -20°C long term. Avoid freeze/thaw cycles.
  • Konopka, Bomar, Winden, Coppola, Jonsson, Gao, Peng, Preuss, Wohlschlegel, Geschwind: "Human-specific transcriptional regulation of CNS development genes by FOXP2." in: Nature, Vol. 462, Issue 7270, pp. 213-7, (2009) (PubMed).

    Ptak, Enard, Wiebe, Hellmann, Krause, Lachmann, Pääbo: "Linkage disequilibrium extends across putative selected sites in FOXP2." in: Molecular biology and evolution, Vol. 26, Issue 10, pp. 2181-4, (2009) (PubMed).

  • 抗原

    FOXP2 (Forkhead Box P2 (FOXP2))

    别名

    FOXP2

    背景

    This gene encodes a member of the forkhead/winged-helix (FOX) family of transcription factors. It is expressed in fetal and adult brain as well as in several other organs such as the lung and gut. The protein product contains a FOX DNA-binding domain and a large polyglutamine tract and is an evolutionarily conserved transcription factor, which may bind directly to approximately 300 to 400 gene promoters in the human genome to regulate the expression of a variety of genes. This gene is required for proper development of speech and language regions of the brain during embryogenesis, and may be involved in a variety of biological pathways and cascades that may ultimately influence language development. Mutations in this gene cause speech-language disorder 1 (SPCH1), also known as autosomal dominant speech and language disorder with orofacial dyspraxia. Multiple alternative transcripts encoding different isoforms have been identified in this gene.

    分子量

    85 kDa

    基因ID

    93986

    UniProt

    O15409
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