FOXC1 抗体 (AA 392-554) (Fluoro647)
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北京 101111
Quick Overview for FOXC1 抗体 (AA 392-554) (Fluoro647) (ABIN7991379)
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 392-554
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原理
- Anti-FOXC1 Antibody Fluoro647 Conjugated
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特异性
- No cross reactivity with other proteins.
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交叉反应 (详细)
- No cross-reactivity with other proteins.
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纯化方法
- Immunogen affinity purified.
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免疫原
- E.coli-derived human FOXC1 recombinant protein (Position: T392-F554).
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亚型
- IgG
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应用备注
- Flow Cytometry, Optimal dilutions should be determined by end users.
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限制
- 仅限研究用
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状态
- Liquid
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缓冲液
- Each vial contains 50 % glycerol, 0.9 % NaCl, 0.2 % Na2HPO4, 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
- At -20°C for one year from date of receipt. Avoid repeated freezing and thawing. Protect from light.
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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
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背景
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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
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基因ID
- 2296
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UniProt
- Q12948
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途径
- Chromatin Binding, Glycosaminoglycan Metabolic Process
抗原
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