Background：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.
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Ideal for studying FOXP3’s roles as a forkhead/winged-helix family transcriptional regulator or its association with immunodeficiency polyendocrinopathy, enteropathy, X-linked syndrome (IPEX), this trusted FOXP3 Rabbit Monoclonal Antibody boosts assay reproducibility for autoimmunity, immunodeficiency, and immune cell biology research. Order WR4112 today to advance your FOXP3-focused experiments with a SEO-verified, high-performance research tool tailored for immunological and transcriptional regulation studies.
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