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FOXC1 抗体 (C-Term)

FOXC1 适用: 人, 小鼠, 斑马鱼 WB, IHC (p), ChIP, EIA 宿主: 山羊 Polyclonal unconjugated
产品编号 ABIN374336
发货至: 中国
  • 抗原 See all FOXC1 抗体
    FOXC1 (Forkhead Box C1 (FOXC1))
    抗原表位
    • 11
    • 8
    • 5
    • 3
    • 3
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    C-Term
    适用
    • 54
    • 33
    • 19
    • 4
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    人, 小鼠, 斑马鱼
    宿主
    • 55
    • 2
    • 1
    山羊
    克隆类型
    • 57
    • 1
    多克隆
    标记
    • 28
    • 7
    • 4
    • 3
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    This FOXC1 antibody is un-conjugated
    应用范围
    • 39
    • 26
    • 8
    • 7
    • 4
    • 4
    • 3
    • 3
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    Western Blotting (WB), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p)), Chromatin Immunoprecipitation (ChIP), Enzyme Immunoassay (EIA)
    序列
    RTSGAFVYDC SKF
    特异性
    This antibody detects FOXC1 / FKHL7 / FREAC3 at C-term.
    交叉反应 (详细)
    Species reactivity (tested):Human, Mouse, Zebrafish.
    纯化方法
    Ammonium Sulphate Precipitation followed by antigen Affinity Chromatography using the immunizing peptide
    免疫原
    Peptide from C-Terminus of the protein sequence according to NP_001444.2. Genename: FOXC1
    Top Product
    Discover our top product FOXC1 Primary Antibody
  • 应用备注
    Peptide ELISA: Limit dilution 1: 32000. Western blot: 0.5-1.5 μg/mL. Approx 55 kDa band observed in Human Bone Marrow lysates(calculated MW of 56.5 kDa according to NP_001444.1). Immunohistochemistry: 3 μg/mL. In paraffin embedded Human Kidney shows nuclearstaining of some cells in the glomeruli.
    Other applications not tested.
    Optimal dilutions are dependent on conditions and should be determined by the user.
    限制
    仅限研究用
  • 浓度
    0.5 mg/mL
    缓冲液
    Tris saline, pH ~7.3, 0.02 % Sodium Azide, 0.5 % BSA
    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.
    注意事项
    Avoid repeated freezing and thawing.
    储存条件
    4 °C/-20 °C
    储存方法
    Store the antibody undiluted at 2-8 °C for one month or (in aliquots) at -20 °C.
  • Doucette, Footz, Walter: "FOXC1 Regulates Expression of Prostaglandin Receptors Leading to an Attenuated Response to Latanoprost." in: Investigative ophthalmology & visual science, Vol. 59, Issue 6, pp. 2548-2554, (2019) (PubMed).

    Fatima, Wang, Uchida, Norden, Liu, Culver, Dietz, Culver, Millay, Mukouyama, Kume: "Foxc1 and Foxc2 deletion causes abnormal lymphangiogenesis and correlates with ERK hyperactivation." in: The Journal of clinical investigation, Vol. 126, Issue 7, pp. 2437-51, (2017) (PubMed).

    Ito, Goping, Berry, Walter: "Dysfunction of the stress-responsive FOXC1 transcription factor contributes to the earlier-onset glaucoma observed in Axenfeld-Rieger syndrome patients." in: Cell death & disease, Vol. 5, pp. e1069, (2014) (PubMed).

  • 抗原
    FOXC1 (Forkhead Box C1 (FOXC1))
    别名
    FOXC1 / FKHL7 / FREAC3 (FOXC1 产品)
    别名
    ARA antibody, FKHL7 antibody, FREAC-3 antibody, FREAC3 antibody, IGDA antibody, IHG1 antibody, IRID1 antibody, RIEG3 antibody, FoxC1 antibody, fkhl7 antibody, freac-3 antibody, freac3 antibody, igda antibody, ihg1 antibody, irid1 antibody, rieg3 antibody, xfd-11 antibody, ara antibody, FOXC1 antibody, foxc1 antibody, Fkh1 antibody, Mf1 antibody, Mf4 antibody, ch antibody, fkh-1 antibody, frkhda antibody, CFKH-1 antibody, XFD-11 antibody, foxc1.2 antibody, id:ibd5079 antibody, forkhead box C1 antibody, forkhead box C1 S homeolog antibody, forkhead box C1 L homeolog antibody, Forkhead box protein C1 antibody, winged helix transcription factor XFD-11 antibody, forkhead box C1b antibody, FOXC1 antibody, Foxc1 antibody, foxc1.S antibody, foxc1 antibody, foxc1.L antibody, foxc1-A antibody, foxc1b antibody
    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.Synonyms: FREAC-3, Forkhead box protein C1, Forkhead-related protein FKHL7, Forkhead-related transcription factor 3
    分子量
    56.8kDa (NP_001444.1).
    基因ID
    2296
    NCBI登录号
    NP_001444
    UniProt
    Q12948
    途径
    Chromatin Binding, Glycosaminoglycan Metabolic Process
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