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- 抗原 See all FOXP2 抗体
- FOXP2 (Forkhead Box P2 (FOXP2))
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适用
- 人
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宿主
- 小鼠
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克隆类型
- 单克隆
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标记
- This FOXP2 antibody is un-conjugated
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应用范围
- Western Blotting (WB), ELISA
- 纯化方法
- purified
- 免疫原
- Purified recombinant fragment of human MAPK3 expressed in E. coli.
- 克隆位点
- 5C11A8
- 亚型
- IgG1
- Top Product
- Discover our top product FOXP2 Primary Antibody
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- 应用备注
- ELISA: 1:10000, WB: 1:500 - 1:2000
- 限制
- 仅限研究用
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- 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
- 4°C, -20°C for long term storage
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Human-specific transcriptional regulation of CNS development genes by FOXP2." in: Nature, Vol. 462, Issue 7270, pp. 213-7, (2009) (PubMed).
: "Linkage disequilibrium extends across putative selected sites in FOXP2." in: Molecular biology and evolution, Vol. 26, Issue 10, pp. 2181-4, (2009) (PubMed).
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Human-specific transcriptional regulation of CNS development genes by FOXP2." in: Nature, Vol. 462, Issue 7270, pp. 213-7, (2009) (PubMed).
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- 抗原
- FOXP2 (Forkhead Box P2 (FOXP2))
- 别名
- FOXP2 (FOXP2 产品)
- 别名
- CAGH44 antibody, SPCH1 antibody, TNRC10 antibody, 2810043D05Rik antibody, AI449000 antibody, CAG-16 antibody, D0Kist7 antibody, RGD1559697 antibody, FOXP2 antibody, spch1 antibody, cagh44 antibody, tnrc10 antibody, xlFoxP2 antibody, foxP2 antibody, foxP antibody, Foxp2 antibody, foxP2b antibody, foxp2a antibody, forkhead box P2 antibody, lmw-gs antibody, forkhead box transcription factor antibody, forkhead box P2 L homeolog antibody, FOXP2 antibody, Foxp2 antibody, foxp2 antibody, foxP2 antibody, foxp1c antibody, foxp2.L antibody
- 背景
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Description: 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.
Aliases: SPCH1, CAGH44, TNRC10, DKFZp686H1726
- 分子量
- 85 kDa
- 基因ID
- 93986
- HGNC
- 93986
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