FOXC1 抗体 (AA 404-553)
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- 抗原 See all FOXC1 抗体
- FOXC1 (Forkhead Box C1 (FOXC1))
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抗原表位
- AA 404-553
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适用
- 人
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宿主
- 兔
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克隆类型
- 多克隆
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标记
- This FOXC1 antibody is un-conjugated
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应用范围
- Western Blotting (WB), Immunohistochemistry (IHC)
- 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
- Top Product
- Discover our top product FOXC1 Primary Antibody
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- 应用备注
- WB,1:100 - 1:1000,IHC,1:50 - 1:100
- 限制
- 仅限研究用
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- 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.
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- 抗原
- FOXC1 (Forkhead Box C1 (FOXC1))
- 别名
- FOXC1 (FOXC1 产品)
- 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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