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FOXC1 抗体 (AA 392-554) (HRP)

This 兔 多克隆 antibody specifically detects FOXC1 in WB, ELISA 和 IHC. It exhibits reactivity toward 人.
产品编号 ABIN7991376
发货至: 中国
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中国
北京 101111
No. 88 KeChuang 6th Street
Beijing Economic Technological Development Area
Room 801-803
4A Biotech Co.,Ltd.
Tel +86 (0512) 65829739 传真 +86 (010) 6788 5057

Quick Overview for FOXC1 抗体 (AA 392-554) (HRP) (ABIN7991376)

抗原

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

适用

  • 64
  • 40
  • 18
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  • 1
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宿主

  • 74
  • 2
  • 1

克隆类型

  • 66
  • 11
多克隆

标记

  • 34
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This FOXC1 antibody is conjugated to HRP

应用范围

  • 49
  • 24
  • 12
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  • 7
  • 3
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  • 1
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Western Blotting (WB), ELISA, Immunohistochemistry (IHC)
  • 抗原表位

    • 12
    • 8
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    • 3
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    • 2
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    • 1
    • 1
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    AA 392-554

    原理

    Anti-FOXC1 Antibody HRP Conjugated

    特异性

    No cross reactivity with other proteins.

    交叉反应 (详细)

    No cross-reactivity with other proteins.

    纯化方法

    Immunogen affinity purified.

    免疫原

    E.coli-derived human FOXC1 recombinant protein (Position: T392-F554).

    亚型

    IgG
  • 应用备注

    Western blot, Optimal dilutions should be determined by end users. Immunohistochemistry (Paraffin-embedded Section), Optimal dilutions should be determined by end users. ELISA, Optimal dilutions should be determined by end users.

    限制

    仅限研究用
  • 状态

    Liquid

    缓冲液

    Each vial contains 50 % glycerol, 0.9 % NaCl, 0.2 % Na2HPO4.

    储存条件

    -20 °C

    储存方法

    At -20°C for one year from date of receipt. Avoid repeated freezing and thawing.

    有效期

    12 months
  • 抗原

    FOXC1 (Forkhead Box C1 (FOXC1))

    别名

    FOXC1

    背景

    Background: Forkhead box C1, also known as?FOXC1, is a?protein?which in humans is encoded by the?FOXC1?gene. It is mapped to 6p25.3. This gene 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.

    Gene Full Name: forkhead box C1

    基因ID

    2296

    UniProt

    Q12948

    途径

    Chromatin Binding, Glycosaminoglycan Metabolic Process
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