-
Product Name
FOXP3 Rabbit mAb
-
Gene ID
50943
-
SwissProt ID
Q9BZS1
-
Gene Name
FOXP3
-
Alternative Names
FOXP3; IPEX; JM2; Forkhead box protein P3; Scurfin
-
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.
-
Research Field
Cell Biology
-
Product Categories
Pathological antibody
-
Host
Rabbit
-
Reactivity
Human
-
Application
IHC-P
-
Dilution Ratio
IHC: 1/100-1/200
-
Molecular Weight
-
-
Clonality
Monoclonal Antibody
-
Clonality No.
R03-2N-9
-
Isotype
IgG
-
Immunogen
A synthesized peptide derived from human FOXP3
-
Purification
Affinity Purified
-
Conjugation
Unconjugated
-
Modification
Unmodified
-
Form
Liquid
-
Buffer System
Liquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide, pH 7.3.
-
Storage
Store at 4°C short term. Aliquot and store at -20°C long term. Avoid freeze/thaw cycles.