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FOXP2 抗体 (AA 657-684)

This anti-FOXP2 antibody is a 兔 多克隆 antibody detecting FOXP2 in WB, ELISA 和 IF. Suitable for 人 和 小鼠.
产品编号 ABIN3030995
发货至: 中国

Quick Overview for FOXP2 抗体 (AA 657-684) (ABIN3030995)

抗原

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

适用

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人, 小鼠

宿主

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  • 7
  • 3
  • 2
  • 1

克隆类型

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  • 10
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多克隆

标记

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This FOXP2 antibody is un-conjugated

应用范围

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

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    • 6
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    • 1
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    AA 657-684

    交叉反应 (详细)

    Expected species reactivity: Rat

    纯化方法

    Antigen affinity purified

    免疫原

    A portion of amino acids 657-684 from the human protein was used as the immunogen for this FOXP2 antibody.

    亚型

    Ig Fraction
  • 应用备注

    Titration of the FOXP2 antibody may be required due to differences in protocols and secondary/substrate sensitivity.\. Western blot: 1:1000,Immunofluorescence: 1:10-1:50

    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 FOXP2 antibody and store frozen at -20°C or colder. Avoid repeated freeze-thaw cycles.
  • 抗原

    FOXP2 (Forkhead Box P2 (FOXP2))

    别名

    FOXP2

    背景

    FOXP2 is 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.

    UniProt

    O15409
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