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FOXC1 抗体 (Internal Region)

The 山羊 多克隆 anti-FOXC1 antibody is suitable to detect FOXC1 in samples from 人, 小鼠 和 Pig. It has been validated for WB 和 EIA.
产品编号 ABIN569579
发货至: 中国
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Quick Overview for FOXC1 抗体 (Internal Region) (ABIN569579)

抗原

See all FOXC1 抗体
FOXC1 (Forkhead Box C1 (FOXC1))

适用

  • 54
  • 41
  • 19
  • 4
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
人, 小鼠, Pig

宿主

  • 64
  • 2
  • 1
山羊

克隆类型

  • 56
  • 11
多克隆

标记

  • 33
  • 7
  • 3
  • 3
  • 3
  • 3
  • 3
  • 3
  • 3
  • 2
  • 1
  • 1
  • 1
  • 1
This FOXC1 antibody is un-conjugated

应用范围

  • 47
  • 23
  • 12
  • 10
  • 10
  • 6
  • 4
  • 3
  • 2
  • 1
  • 1
  • 1
  • 1
Western Blotting (WB), Enzyme Immunoassay (EIA)
  • 抗原表位

    • 8
    • 6
    • 5
    • 3
    • 3
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    Internal Region

    序列

    C-DAVKDKEEKD RLH

    特异性

    Recognizes FOXC1 (internal).

    交叉反应 (详细)

    Species reactivity (expected):Pig, Mouse.
    Species reactivity (tested):Human.

    纯化方法

    Ammonium Sulphate Precipitation followed by Antigen Affinity Chromatography using the immunizing peptide.

    免疫原

    Dynthetic peptide from an internal region of Human FOXC1 (NP_001444.2). Genename: FOXC1
  • 应用备注

    Optimal working dilution should be determined by the investigator.

    限制

    仅限研究用
  • 浓度

    0.5 mg/mL

    缓冲液

    Tris saline, pH 7.3 containing 0.02 % Sodium Azide as preservative and 0.5 % BSA as stabilizer.

    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 for longer.
  • 抗原

    FOXC1 (Forkhead Box C1 (FOXC1))

    别名

    FOXC1 / FKHL7 / FREAC3

    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_001444.2).

    基因ID

    2296

    NCBI登录号

    NP_001444

    UniProt

    Q12948

    途径

    Chromatin Binding, Glycosaminoglycan Metabolic Process
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