|ChIP assay (ChIP)||Assay dependent|
|Immunocytochemistry (ICC)||2-4 ug/ml|
|Immunohistochemistry (Paraffin) (IHC (P))||0.3-1 µg/ml|
|Western Blot (WB)||Assay dependent|
|Tested Species reactivity||Human|
|Host / Isotype||Goat / IgG|
|Immunogen||Synthetic peptide corresponding to the C terminus residues S Q R P S R C S N P T P G P of human FOXP3.|
|Purification||Antigen affinity chromatography|
|Storage buffer||TBS, pH 7.3, with 0.5% BSA|
|Contains||0.02% sodium azide|
|Storage conditions||-20° C, Avoid Freeze/Thaw Cycles|
This antibody is predicted to react with canine and porcine based on sequence homology.
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.
For Research Use Only. Not for use in diagnostic procedures. Not for resale without express authorization.
Protein Aliases: AIID; DIETER; Forkhead box P3; Forkhead box protein P3; foxp3; FOXP3delta7; immune dysregulation, polyendocrinopathy, enteropathy, X-linked; immunodeficiency, polyendocrinopathy, enteropathy, X-linked; IPEX; JM2; PIDX; SCURFIN; XPID
Gene Aliases: AIID; DIETER; FOXP3; IPEX; JM2; PIDX; XPID
UniProt ID: (Human) Q9BZS1
Entrez Gene ID: (Human) 50943
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