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FOXC1 抗体 (AA 404-553)

This anti-FOXC1 antibody is a 兔 多克隆 antibody detecting FOXC1 in WB 和 IHC. Suitable for 人.
产品编号 ABIN1679876
发货至: 中国

Quick Overview for FOXC1 抗体 (AA 404-553) (ABIN1679876)

抗原

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

适用

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宿主

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克隆类型

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多克隆

标记

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This FOXC1 antibody is un-conjugated

应用范围

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Western Blotting (WB), Immunohistochemistry (IHC)
  • 抗原表位

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    AA 404-553

    序列

    AAGERGGHLQ GAPGGAGGSA VDDPLPDYSL PPVTSSSSSS LSHGGGGGGG GGGQEAGHHP AAHQGRLTSW YLNQAGGDLG HLASAAAAAA AAGYPGQQQN FHSVREMFES QRIGLNNSPV NGNSSCQMAF PSSQSLYRTS GAFVYDCSKF

    交叉反应

    人, 小鼠, 大鼠

    产品特性

    Polyclonal Antibodies

    纯化方法

    Affinity purification

    免疫原

    Recombinant fusion protein containing a sequence corresponding to amino acids 404-553 of human FOXC1 (NP_001444.2).

    亚型

    IgG
  • 应用备注

    WB,1:100 - 1:1000,IHC,1:50 - 1:100

    限制

    仅限研究用
  • 缓冲液

    PBS with 0.02 % sodium azide,50 % glycerol, pH 7.3.

    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.

    储存条件

    -20 °C

    储存方法

    Store at -20°C. Avoid freeze / thaw cycles.
  • 抗原

    FOXC1 (Forkhead Box C1 (FOXC1))

    别名

    FOXC1

    背景

    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.,FOXC1,ARA,ASGD3,FKHL7,FREAC-3,FREAC3,IGDA,IHG1,IRID1,RIEG3,Epigenetics & Nuclear Signaling,Transcription Factors,Cell Biology & Developmental Biology,FOXC1

    分子量

    56 kDa

    基因ID

    2296

    UniProt

    Q12948

    途径

    Chromatin Binding, Glycosaminoglycan Metabolic Process
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