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人 FOXP3 抗体对
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人 FOXP3 抗体对

01AB03109

Forkhead box protein P3 (FOXP3) is a master regulator of regulatory T cell (Treg) development and function, playing a crucial role in maintaining immune homeostasis and self-tolerance. It contains several functional domains, including a proline-rich N-terminal domain, a zinc-finger and leucine-zipper domain, and a C-terminal forkhead domain responsible for DNA binding. FOXP3 acts as both a transcriptional activator and repressor, interacting with various proteins to modulate gene expression in Tregs. It is essential for the stability and suppressive function of Tregs, which suppress excessive immune responses and prevent autoimmunity. Mutations or dysregulation of FOXP3 can lead to severe autoimmune diseases like IPEX syndrome, characterized by multi-organ inflammation and autoantibody production. Additionally, altered FOXP3 expression has been linked to cancer, where it may influence tumor immunity and progression.

Human
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技术参数

靶点基因名
FOXP3
基因别名
IPEX
蛋白别名
forkhead box P3; FOXP3
UniProt
Q9BZS1
物种
Human

产品详情

靶点名称
FOXP3
蛋白名称
forkhead box P3
蛋白别名
Forkhead box protein P3; Scurfin) [Cleaved into: Forkhead box protein P3; C-terminally processed; Forkhead box protein P3 41 kDa form]
靶点基因名
FOXP3
基因别名
IPEX
UniProt
Q9BZS1
来源物种
Homo sapiens (Human)
物种反应性
Human

背景介绍

Forkhead box protein P3 (FOXP3) is a master regulator of regulatory T cell (Treg) development and function, playing a crucial role in maintaining immune homeostasis and self-tolerance. It contains several functional domains, including a proline-rich N-terminal domain, a zinc-finger and leucine-zipper domain, and a C-terminal forkhead domain responsible for DNA binding. FOXP3 acts as both a transcriptional activator and repressor, interacting with various proteins to modulate gene expression in Tregs. It is essential for the stability and suppressive function of Tregs, which suppress excessive immune responses and prevent autoimmunity. Mutations or dysregulation of FOXP3 can lead to severe autoimmune diseases like IPEX syndrome, characterized by multi-organ inflammation and autoantibody production. Additionally, altered FOXP3 expression has been linked to cancer, where it may influence tumor immunity and progression.