Forkhead Box C1 (FOXC1) Peptide
FOXC1
适用: 人
宿主: 合成
BP, WB
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- 抗原 See all FOXC1 products
- FOXC1 (Forkhead Box C1 (FOXC1))
- 宿主
- 人
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资源
- 合成
- 应用范围
- Blocking Peptide (BP), Western Blotting (WB)
- 产品特性
- This is a synthetic peptide designed for use in combination with anti-FOXC1 antibody (Catalog #: ARP32300_T100). 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
- FOXC1 (Forkhead Box C1 (FOXC1))
- 别名
- ARA Peptide, FKHL7 Peptide, FREAC-3 Peptide, FREAC3 Peptide, IGDA Peptide, IHG1 Peptide, IRID1 Peptide, RIEG3 Peptide, FoxC1 Peptide, fkhl7 Peptide, freac-3 Peptide, freac3 Peptide, igda Peptide, ihg1 Peptide, irid1 Peptide, rieg3 Peptide, xfd-11 Peptide, ara Peptide, FOXC1 Peptide, foxc1 Peptide, Fkh1 Peptide, Mf1 Peptide, Mf4 Peptide, ch Peptide, fkh-1 Peptide, frkhda Peptide, CFKH-1 Peptide, XFD-11 Peptide, foxc1.2 Peptide, id:ibd5079 Peptide, forkhead box C1 Peptide, forkhead box C1 S homeolog Peptide, forkhead box C1 L homeolog Peptide, Forkhead box protein C1 Peptide, winged helix transcription factor XFD-11 Peptide, forkhead box C1b Peptide, FOXC1 Peptide, Foxc1 Peptide, foxc1.S Peptide, foxc1 Peptide, foxc1.L Peptide, foxc1-A Peptide, foxc1b Peptide
- 背景
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FOXC1 belongs to the forkhead family of transcription factors which is characterized by a distinct DNA-binding forkhead domain. The specific function of this gene has not yet been determined, however, it has been shown to play a role in the regulation of embryonic and ocular development. Mutations in this gene cause various glaucoma phenotypes including primary congenital glaucoma, autosomal dominant iridogoniodysgenesis anomaly, and Axenfeld-Rieger anomaly.
Alias Symbols: ARA, IGDA, IHG1, FKHL7, IRID1, RIEG3, FREAC3, FREAC-3
Protein Interaction Partner: HMGB1
Protein Size: 553 - 分子量
- 57 kDa
- 基因ID
- 2296
- NCBI登录号
- NM_001453, NP_001444
- UniProt
- Q12948
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