Western blot analysis using anti-FOXP3 (mouse), pAb (Prod. No. AG-25A-0020) at 1:3000 dilution. 1: Mouse FOXP3 (His-tagged). 2: Transfected mouse FOXP3 cell lysate (HEK 293). 3: Mouse T lymphocyte (CD4+) cell lysate. 4: PHA treate
anti-FOXP3 (mouse), pAb
AG-25A-0020
ApplicationsWestern Blot, ELISA
Product group Antibodies
ReactivityMouse
TargetFoxp3
Overview
- SupplierAdipoGen Life Sciences
- Product Nameanti-FOXP3 (mouse), pAb
- Delivery Days Customer10
- Antibody SpecificityRecognizes mouse FOXP3. Detects a band of ~46-49kDa by Western blot.
- ApplicationsWestern Blot, ELISA
- CertificationResearch Use Only
- ClonalityPolyclonal
- Concentration1 mg/ml
- FormulationLiquid
- Gene ID20371
- Target nameFoxp3
- Target descriptionforkhead box P3
- Target synonymsforkhead box protein P3; JM2; scu; scurfin; scurfy; sf
- HostRat
- Protein IDQ99JB6
- Protein NameForkhead box protein P3
- Scientific DescriptionFOXP3 is involved in immune system responses. It functions as the master regulator in the development and function of regulatory T cells. FOX proteins belong to the forkhead/winged-helix family of transcriptional regulators and are presumed to exert control via similar DNA binding interactions during transcription. Defects in FOXP3 are the cause of immunodeficiency polyendocrinopathy, enteropathy, X-linked syndrome (IPEX); 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. - Polyclonal Antibody. Recognizes mouse FOXP3. Detects a band of ~46-49kDa by Western blot. Source: Rat. Applications: ELISA, WB. Liquid. 0.2microm-filtered solution in PBS, pH 7.4. Contains no preservatives. FOXP3 is involved in immune system responses. It functions as the master regulator in the development and function of regulatory T cells. FOX proteins belong to the forkhead/winged-helix family of transcriptional regulators and are presumed to exert control via similar DNA binding interactions during transcription. Defects in FOXP3 are the cause of immunodeficiency polyendocrinopathy, enteropathy, X-linked syndrome (IPEX); 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.
- ReactivityMouse
- Storage Instruction-20°C,2°C to 8°C
- UNSPSC12352203