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.
仕様
Synonyms:AIID,DIETER,Forkhead box P3,Forkhead box protein P3,FOXP3,FOXP3,FOXP3delta7,Immune dysregulation polyendocrinopathy enteropathy X linked,Immunodeficiency polyendocrinopathy enteropathy X linked,IPEX,JM2,MGC141961,MGC141963,OTTHUMP00000025832,OTTHUMP00000025833,OTTHUMP00000226737,PIDX,Scurfin,XPID
Host:Rabbit
Reactivity:Human,Mouse
Applications:WB,ELISA
Concentration:1.5mg/mL
Immunogen:Synthetic peptide of human FOXP3
Purification Method:Affinity purification
Clonality:Polyclonal
Conjugation:Unconjugated
Buffer:PBS with 0.05% sodium azide, 50% glycerol, PH7.3
Dilution:WB 1:500-1:2000
Swissprot:Q9BZS1
Isotype:IgG
Research Areas:Cancer, Cell Biology, Epigenetics and Nuclear Signaling, Immunology