FOXP3 mouse mAb

• Background:

  Forkhead box P3 (FOXP3) Homo sapiens 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:

  AIID; DIETER; Forkhead box P3; Forkhead box protein P3; foxp3; foxp3; FOXP3_HUMAN; FOXP3delta7; Immune dysregulation polyendocrinopathy enteropathy X linked; Immunodeficiency polyendocrinopathy enteropathy X linked; IPEX; JM2; MGC141961; MGC141963; OTTHUMP00000025832; OTTHUMP00000025833; OTTHUMP00000226737; PIDX; SCURFIN; XPID.

• Gene ID:

  50943

• Swiss Prot:

  Q9BZS1

• Clonality:

  Monoclonal

• Source:

  Mouse

• Applications:

  WB; ICC

• Dilution:

  Wb 1:300 icc 1:100

• Buffer:

  Liquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.

• Molecular Weight:

  47

• Storage Conditions:

  -20°C/1 year

• Protein Weight:

  47