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首页 > 产品中心 > 抗体系列 > 一抗

货号:GZ8191

FOXP3 (13S19) Rabbit Monoclonal Antibody

FOXP3;IPEX;JM2;Forkhead box protein P3;Scurfin

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别名 FOXP3;IPEX;JM2;Forkhead box protein P3;Scurfin
基因名称 FOXP3
蛋白名称 Forkhead box protein P3
推荐应用
反应物种 Human,Mouse
存储缓冲液 PBS, 50% glycerol, 0.05% Proclin 300, 0.05%BSA
Human Gene Link http://www.ncbi.nlm.nih.gov/sites/entrez?db=gene&term=50943
Human Swissprot No. Q9BZS1
Human Swissprot Link http://www.uniprot.org/uniprotkb/Q9BZS1/entry
Mouse Gene ID 20371
Mouse Gene Link http://www.ncbi.nlm.nih.gov/sites/entrez?db=gene&term=20371
Mouse Swissprot No. Q99JB6
Mouse Swissprot Link http://www.uniprot.org/uniprot/Q99JB6
稀释度 IHC-P 1:200-1:1000,WB 1:1000-1:5000,IF-P/IF-F/IF-ICC 1:200-1:1000,ELISA 1:5000-1:20000,IP 1:50-1:200
参考分子量 47kDa
预测分子量 47kDa
运输及保存条件 Biological ice bag transportation. Store at -20°C for at least 12 months(Do not lower than -25°C). Avoid freeze/thaw cycles
宿主 Rabbit
同种型 Monoclonal, rabbit, IgG, Kappa
背景介绍 The protein encoded by this gene is a member of the forkhead/winged-helix family of transcriptional regulators. Defects in this gene are the cause of immunodeficiency polyendocrinopathy, enteropathy, X-linked syndrome (IPEX), also known as X-linked autoimmunity-immunodeficiency syndrome. Alternatively spliced transcript variants encoding different isoforms have been identified. [provided by RefSeq, Jul 2008],
功能 disease:Defects in FOXP3 are the cause of immunodeficiency polyendocrinopathy, enteropathy, X-linked syndrome (IPEX) [MIM:304790]; also known as X-linked autoimmunity-immunodeficiency syndrome. IPEX is characterized by neonatal onset insulin-dependent diabetes mellitus, infections, secretory diarrhea, trombocytopenia, anemia and eczema. It is usually lethal in infancy.,function:Probable transcription factor. Plays a critical role in the control of immune response.,online information:FOXP3 entry,online information:FOXP3 mutation db,similarity:Contains 1 C2H2-type zinc finger.,similarity:Contains 1 fork-head DNA-binding domain.,
纯化 Protein A
Clonality Monoclonal

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