FOXC1 抗体 (AA 392-554)
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北京 101111
Quick Overview for FOXC1 抗体 (AA 392-554) (ABIN7874618)
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
- FOXC1 Antibody
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纯化方法
- Affinity purified
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免疫原
- A human recombinant protein (amino acids T392-F554) was used as the immunogen for the FOXC1 antibody.
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亚型
- IgG
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anti-Forkhead Box C1 (FOXC1) (C-Term) antibody
Verified FOXC1 适用: 人 ELISA, IF, FACS 宿主: 山羊 Polyclonal unconjugated
anti-Forkhead Box C1 (FOXC1) antibodyFOXC1 适用: 人, 小鼠, 大鼠 WB, ELISA, IF, ICC 宿主: 兔 Polyclonal unconjugated
anti-Forkhead Box C1 (FOXC1) (AA 1-79) antibodyFOXC1 适用: 人 WB, ELISA, IF 宿主: 兔 Polyclonal unconjugated
anti-Forkhead Box C1 (FOXC1) (AA 488-515), (C-Term) antibodyFOXC1 适用: 人 WB, FACS 宿主: 兔 Polyclonal RB22897 unconjugated
anti-Forkhead Box C1 (FOXC1) (Center) antibodyFOXC1 适用: 人, 小鼠, 大鼠, 小鸡 WB 宿主: 兔 Polyclonal unconjugated
anti-Forkhead Box C1 (FOXC1) (AA 101-200) antibodyFOXC1 适用: 人, 小鼠, 大鼠, 山羊 WB, ELISA, FACS, IHC (p), IF (cc), IF (p), IHC (fro) 宿主: 兔 Polyclonal unconjugated
anti-Forkhead Box C1 (FOXC1) (AA 62-186) antibodyFOXC1 适用: 小鼠 WB, IHC, IP, ICC 宿主: 兔 Polyclonal unconjugated
anti-Forkhead Box C1 (FOXC1) (Internal Region) antibodyVerified FOXC1 适用: 人 WB, ELISA 宿主: 山羊 Polyclonal unconjugated
anti-Forkhead Box C1 (FOXC1) (AA 406-455) antibodyFOXC1 适用: 人, 小鼠 WB 宿主: 兔 Polyclonal unconjugated
anti-Forkhead Box C1 (FOXC1) (AA 464-553) antibodyFOXC1 适用: 人 WB, ELISA 宿主: 小鼠 Monoclonal 4D11 unconjugated
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应用备注
- Optimal dilution of the FOXC1 antibody should be determined by the researcher.
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限制
- 仅限研究用
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状态
- Lyophilized
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缓冲液
- 0.5 mg/mL if reconstituted with 0.2 mL sterile DI water
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储存条件
- 4 °C,-20 °C
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储存方法
- After reconstitution, the FOXC1 antibody can be stored for up to one month at 4oC. For long-term, aliquot and store at -20oC. Avoid repeated freezing and thawing.
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- FOXC1 (Forkhead Box C1 (FOXC1))
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别名
- FOXC1
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背景
- 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.
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UniProt
- Q12948
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途径
- Chromatin Binding, Glycosaminoglycan Metabolic Process
抗原
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