
IHC-P analysis of human spleen tissue using GTX04725 FOXP3 antibody. Left : Primary antibody Right : No primary antibody Antigen retrieval : Heat mediated citrate buffer (pH 6.0) Dilution : 8 μg/mL
FOXP3 antibody
GTX04725
ApplicationsFlow Cytometry, ImmunoFluorescence, Western Blot, ELISA, ImmunoCytoChemistry, ImmunoHistoChemistry, ImmunoHistoChemistry Paraffin
Product group Antibodies
ReactivityHuman
TargetFOXP3
Overview
- SupplierGeneTex
- Product NameFOXP3 antibody
- Delivery Days Customer9
- Application Supplier NoteWB: 1-3 microg/mL. ICC/IF: 10 microg/ml. IHC-P: 6-8 microg/mL. FCM: 10 microg/mL. ELISA: 1:8000. *Optimal dilutions/concentrations should be determined by the researcher.Not tested in other applications.
- ApplicationsFlow Cytometry, ImmunoFluorescence, Western Blot, ELISA, ImmunoCytoChemistry, ImmunoHistoChemistry, ImmunoHistoChemistry Paraffin
- CertificationResearch Use Only
- ClonalityPolyclonal
- Concentration0.5 mg/ml
- ConjugateUnconjugated
- Gene ID50943
- Target nameFOXP3
- Target descriptionforkhead box P3
- Target synonymsAIID, DIETER, IPEX, JM2, PIDX, XPID, forkhead box protein P3, FOXP3delta7, immune dysregulation, polyendocrinopathy, enteropathy, X-linked, immunodeficiency, polyendocrinopathy, enteropathy, X-linked
- HostGoat
- IsotypeIgG
- Protein IDQ9BZS1
- Protein NameForkhead box protein P3
- Scientific DescriptionThe 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. [provided by RefSeq, Jul 2008]
- ReactivityHuman
- Storage Instruction-20°C or -80°C,2°C to 8°C
- UNSPSC41116161








