Species: | Rabbit |
Applications: | WB IHC IF IP |
Immunogen Range: | A synthetic peptide derived from human FOXP3 |
Clonality: | Polyclonal Antibody |
Isotype: | IgG |
GENE ID: | 50943 |
Swiss Prot: | Q9BZS1 |
Synonyms: | Forkhead box P3 antibodyForkhead box protein P3 antibodyfoxp3 antibodyfoxp3 antibodyFOXP3_HUMAN antibodyFOXP3delta7 antibody |
Purification: | Affinity purification |
Storage: | Store at -20°C or -80°C in PBS with 0.02% sodium azide and 50% glycerol. Avoid freeze/thaw cycles. |
Background: | Defects in FOXP3 are the cause of immunodeficiency polyendocrinopathy, enteropathy, X-linked syndrome (IPEX) [MIM:304790]; also known as X-linked autoimmunity-immunodeficiency syndrome. IPEX is characterized by neonatal onset insulin-dependent diabetes mellitus, infections, secretory diarrhea, trombocytopenia, anemia and eczema. It is usually lethal in infancy. |
Caculated MW: | 47 kDa |
Observed MW: | Refer to Figures |
Applications: |
WB 1:500-1:2000 IHC 1:50-1:200 IF 1:100-1:500 |
Reacitivity: | Human |