Recombinant Human FOXP3 protein, His-tagged
| Cat.No. : | FOXP3-53H |
| Product Overview : | Recombinant Human FOXP3, transcript variant 2, fused with His tag at N-terminal was expressed in E. coli. |
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| Species : | Human |
| Source : | E.coli |
| Tag : | His |
| 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. |
| Form : | 25mM Tris, pH8.0, 150 mM NaCl, 10% glycerol, 1 % Sarkosyl. |
| Molecular Mass : | 43.2 kDa |
| Purity : | >80% as determined by SDS-PAGE and Coomassie blue staining |
| Concentration : | >50 ug/mL as determined by microplate BCA method |
| Gene Name | FOXP3 forkhead box P3 [ Homo sapiens ] |
| Official Symbol | FOXP3 |
| Synonyms | FOXP3; forkhead box P3; immune dysregulation, polyendocrinopathy, enteropathy, X linked , IPEX; forkhead box protein P3; AIID; DIETER; JM2; PIDX; SCURFIN; XPID; scurfin; FOXP3delta7; immunodeficiency, polyendocrinopathy, enteropathy, X-linked; immune dysregulation, polyendocrinopathy, enteropathy, X-linked; IPEX; MGC141961; MGC141963; |
| Gene ID | 50943 |
| mRNA Refseq | NM_001114377 |
| Protein Refseq | NP_001107849 |
| MIM | 300292 |
| UniProt ID | Q9BZS1 |
| Chromosome Location | Xp11.23 |
| Pathway | Calcineurin-regulated NFAT-dependent transcription in lymphocytes, organism-specific biosystem; IL2 signaling events mediated by STAT5, organism-specific biosystem; |
| Function | DNA binding, bending; NF-kappaB binding; NFAT protein binding; chromatin binding; double-stranded DNA binding; histone acetyltransferase binding; histone deacetylase binding; metal ion binding; protein binding; protein heterodimerization activity; protein homodimerization activity; sequence-specific DNA binding |
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Not For Human Consumption!
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