| No | Size | Price | Availability | |
| ARP50943-61 | 50ul | 1500.00 | In Stock |  |
| ARP50943-61 | 100ul | 2000.00 | In Stock | |
| Source: | Rabbit | Gene Id: | 50943 |
| Isotype: | IgG | Swiss Prot: | Q9BZS1 |
| purity: | Affinity purification |
| 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. |
| Reactivity | Human |
| Tested applications | WB IHC IF IP |
| Clonality | Polyclonal Antibody |
| Calculated MW | 47 kDa |
| Recommended Dilutions |
WB 1:500-1:2000
IHC 1:50-1:200
IF 1:100-1:500
|
| Immunogen | A synthetic peptide derived from human FOXP3 |
| Storage | Store at -20°C or -80°C in PBS with 0.02% sodium azide and 50% glycerol. Avoid freeze/thaw cycles. |
| Synonym | Forkhead box P3 antibodyForkhead box protein P3 antibodyfoxp3 antibodyfoxp3 antibodyFOXP3_HUMAN antibodyFOXP3delta7 antibody |
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