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FOXP3 rabbit pAb

CAT: 0855-ES4176-01Size: 50 µLDry Ice: NoHazardous: No
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CAT#:0855-ES4176-01Size:50 µL
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Background
The 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]
Description
The 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],
Product Name Alternative
FOXP3; IPEX; JM2; Forkhead box protein P3; Scurfin
UniProt
Q9BZS1
Swiss Prot
Q9BZS1
Reactivity
Human; Mouse; Rat; Pig
Immunogen
The antiserum was produced against synthesized peptide derived from the C-terminal region of human FOXP3. AA range:381-430
Target
FOXP3
Clonality
Polyclonal
Source
Rabbit
Applications
WB; IHC; IF; ELISA
Concentration
1 mg/ml
Dilution
Western Blot: 1/500 - 1/2000. IHC-p: 1/100-1/300. ELISA: 1/20000. Not yet tested in other applications.
Buffer
-20°C/1 year
Molecular Weight
47kD
Storage Conditions
-20°C/1 year
Observed Molecular Weight
47kD
Fragment
IgG
Subcellular Location
Nucleus . Cytoplasm . Predominantly expressed in the cytoplasm in activated conventional T-cells whereas predominantly expressed in the nucleus in regulatory T-cells (Treg) . The 41 kDa form derived by proteolytic processing is found exclusively in the chromatin fraction of activated Treg cells (By similarity) . .
Other Product Names
FOXP3; IPEX; JM2; Forkhead box protein P3; Scurfin
Gene ID (Human)
50943

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