Purified recombinant fragment of human FOXP3 expressed in E. Coli.
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]
WB: 1/500 - 1/2000.*Optimal dilutions/concentrations should be determined by the researcher.Not tested in other applications., ELISA: 1/10000.*Optimal dilutions/concentrations should be determined by the researcher.Not tested in other applications.
Source / Host
Store as concentrated solution. Centrifuge briefly prior to opening vial. For short-term storage (1-2 weeks), store at 4-8ºC. For long-term storage, aliquot and store at -20-8ºC or below. Avoid multiple freeze-thaw cycles.
Substrate / Buffer
Ascites, 0.03% sodium azide
For In vitro laboratory use only. Not for any clinical, therapeutic, or diagnostic use in humans or animals. Not for animal or human consumption.
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