Forkhead Box P2 (FOXP2) Peptide
FOXP2
适用: 人
宿主: 合成
BP, WB, IHC
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- 抗原 See all FOXP2 products
- FOXP2 (Forkhead Box P2 (FOXP2))
- 宿主
- 人
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资源
- 合成
- 应用范围
- Blocking Peptide (BP), Western Blotting (WB), Immunohistochemistry (IHC)
- 产品特性
- This is a synthetic peptide designed for use in combination with anti-FOXP2 antibody (Catalog #: ARP33750_P050). It may block above mentioned antibody from binding to its target protein in western blot and/or immunohistochecmistry under proper experimental settings. There is no guarantee for its use in other applications.
- 纯化方法
- Purified
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- 应用备注
- Each Investigator should determine their own optimal working dilution for specific applications.
- 限制
- 仅限研究用
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- 状态
- Lyophilized
- 溶解方式
- Add 100 μL of sterile PBS. Final peptide concentration is 1 mg/mL in PBS.
- 浓度
- 1 mg/mL
- 缓冲液
- Final peptide concentration is 1 mg/mL in PBS.
- 注意事项
- Avoid repeated freeze-thaw cycles.
- 储存条件
- -20 °C
- 储存方法
- For longer periods of storage, store at -20°C. Avoid repeat freeze-thaw cycles.
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- 抗原
- FOXP2 (Forkhead Box P2 (FOXP2))
- 别名
- CAGH44 Peptide, SPCH1 Peptide, TNRC10 Peptide, 2810043D05Rik Peptide, AI449000 Peptide, CAG-16 Peptide, D0Kist7 Peptide, RGD1559697 Peptide, FOXP2 Peptide, spch1 Peptide, cagh44 Peptide, tnrc10 Peptide, xlFoxP2 Peptide, foxP2 Peptide, foxP Peptide, Foxp2 Peptide, foxP2b Peptide, foxp2a Peptide, forkhead box P2 Peptide, lmw-gs Peptide, forkhead box transcription factor Peptide, forkhead box P2 L homeolog Peptide, FOXP2 Peptide, Foxp2 Peptide, foxp2 Peptide, foxP2 Peptide, foxp1c Peptide, foxp2.L Peptide
- 背景
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FOXP2 is an evolutionarily conserved transcription factor expressed in fetal and adult brain. This transcription factor is a member of the forkhead/winged-helix (FOX) family of transcription factors, and contains a FOX DNA-binding domain and a large polyglutamine tract. Members of the FOX family of transcription factors are regulators of embryogenesis. The product of this gene is thought to be required for proper development of speech and language regions of the brain during embryogenesis. Although a point mutation in this gene has been associated with the KE pedigree segregating developmental verbal dyspraxia, no association between mutations in this gene and another speech disorder, autism, has been found. Four alternative transcripts encoding three different isoforms have been identified.
Alias Symbols: SPCH1, CAGH44, TNRC10
Protein Interaction Partner: FOXP1,FOXP4,CTBP1,FOXP1,FOXP2,FOXP4,GATAD2B
Protein Size: 715 - 分子量
- 80 kDa
- 基因ID
- 93986
- NCBI登录号
- NM_014491, NP_055306
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