FOXC1 抗体 (AA 151-200)
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北京 101111
Quick Overview for FOXC1 抗体 (AA 151-200) (ABIN1533852)
抗原
See all FOXC1 抗体适用
宿主
克隆类型
标记
应用范围
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抗原表位
- AA 151-200
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原理
- FoxC1/2 Antibody
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特异性
- FoxC1/2 Polyclonal Antibody detects endogenous levels of FoxC1/2 protein.
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纯化方法
- The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.
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纯度
- > 95 %
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免疫原
- The antiserum was produced against synthesized peptide derived from human FOXC1/2. AA range:151-200
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亚型
- IgG
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应用备注
- WB 1:500 - 1:2000. IHC 1:100 - 1:300. IF 1:200 - 1:1000. ELISA: 1:40000. Not yet tested in other applications.
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限制
- 仅限研究用
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状态
- Liquid
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浓度
- 1 mg/mL
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缓冲液
- Liquid in PBS containing 50 % glycerol, 0.5 % BSA and 0.02 % sodium azide.
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储存液
- Sodium azide
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注意事项
- This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
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储存条件
- -20 °C
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储存方法
- Store at -20°C/1 year
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有效期
- 12 months
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- FOXC1 (Forkhead Box C1 (FOXC1))
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别名
- FOXC1/2
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背景
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Synonyms: FOXC1, FKHL7, FREAC3, Forkhead box protein C1, Forkhead-related protein FKHL7, Forkhead-related transcription factor 3, FREAC-3, FOXC2, FKHL14, MFH1, Forkhead box protein C2, Forkhead-related protein FKHL14, Mesenchyme fork head protein 1,
Background: 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. [provided by RefSeq, Jul 2008],
Gene Name: FOXC1/FOXC2
Protein Name: Forkhead box protein C1/2
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分子量
- 56 kDa
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基因ID
- 2296, 2303
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OMIM
- 601090
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UniProt
- Q12948
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途径
- Chromatin Binding, Glycosaminoglycan Metabolic Process
抗原
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