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Forkhead Box C1 (FOXC1) Peptide

FOXC1 适用: 人 宿主: 合成 BP, WB
产品编号 ABIN976991
发货至: 中国
  • 抗原 See all FOXC1 products
    FOXC1 (Forkhead Box C1 (FOXC1))
    宿主
    资源
    • 8
    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
  • 应用备注
    Each Investigator should determine their own optimal working dilution for specific applications.
    限制
    仅限研究用
  • 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.
  • 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
    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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