|Immunohistochemistry (Paraffin) (IHC (P))||1:50|
|Western Blot (WB)||1 µg/ml|
|Tested Species reactivity||Human, Rat|
|Host / Isotype||Mouse / IgG1|
|Immunogen||Synthetic peptide derived from residues 400 to the C-terminus of Human FOXP3.|
|Storage buffer||5.88% citric acid/tris HCl, pH 7.5, with 2.9% NaCl|
|Contains||0.02% sodium azide|
|Storage conditions||-20° C, Avoid Freeze/Thaw Cycles|
Heat mediated antigen retrieval recommended prior to tissue staining.
This antibody is predicted to react with mouse 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 , 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: Forkhead box protein P3; FOXP3delta7; immune dysregulation, polyendocrinopathy, enteropathy, X-linked; immunodeficiency, polyendocrinopathy, enteropathy, X-linked; JM2, AIID, DIETER, IPEX, MGC141961, MGC141963, PIDX, XPID, FOXP3delta7; Scurfin
Gene Aliases: AIID; DIETER; FOXP3; IPEX; JM2; PIDX; XPID
UniProt ID: (Human) Q9BZS1
Entrez Gene ID: (Human) 50943
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