FOXP3 rabbit pAb

• 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],

• 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

• 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.

• 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