|Flow Cytometry (Flow)||6ug/ml|
|Tested Species reactivity||Human, Mouse|
|Host / Isotype||Mouse / IgG1|
|Immunogen||Full-length His-tagged recombinant murine FoxP3|
|Conjugate||Alexa Fluor® 647|
|Storage buffer||PBS, pH 7.4|
|Contains||15mM sodium azide|
|Storage conditions||4° C, store in dark, DO NOT FREEZE!|
FoxP3 (Forkhead box protein 3), a highly conserved forkhead/winged-helix transcription factor, plays a crucial role in maintaining immune homeostasis by governing the development and function of regulatory T cells. It is constitutively expressed at high level in CD25+ CD4+ Treg cells and at low level in a CD25- CD4+ Treg cell subset. Defects in gene encoding FoxP3 protein cause the scurfy phenotype in mice, and in human the IPEX syndrome (immune dysfunction, polyendocrinopathy, enteropathy, X-linked syndrome), also known as X-linked autoimmunity-allergic dysregulation (XLAAD) syndrome.
For Research Use Only. Not for use in diagnostic procedures. Not for resale without express authorization.
Protein Aliases: AIID; DIETER; enteropathy; Forkhead box protein P3; FOXP3delta7; immune dysregulation; immune dysregulation, polyendocrinopathy, enteropathy, X-linked; immunodeficiency; immunodeficiency, polyendocrinopathy, enteropathy, X-linked; IPEX; JM2; PIDX; polyendocrinopathy; Scurfin; scurfy; X-linked; XPID
Gene Aliases: AIID; DIETER; FOXP3; IPEX; JM2; PIDX; scurfin; sf; XPID
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