FOXC1 (NM_001453) Human Recombinant Protein
CAT#: TP761578
Purified recombinant protein of Human forkhead box C1 (FOXC1), full length, with N-terminal GST and C-terminal HIS tag, expressed in E. coli, 50ug
Other products for "FOXC1"
Specifications
| Product Data | |
| Species | Human |
| Expression Host | E. coli |
| Expression cDNA Clone or AA Sequence |
A DNA sequence encoding human full-length FOXC1
|
| Tag | N-GST and C-His |
| Predicted MW | 84.6 kDa |
| Concentration | >50 ug/mL as determined by microplate BCA method |
| Purity | > 80% as determined by SDS-PAGE and Coomassie blue staining |
| Buffer | 25mM Tris, pH8.0,150mM NaCl,10% glycerol,1%Sarkosyl. |
| Storage | Store at -80°C. |
| Stability | Stable for 12 months from the date of receipt of the product under proper storage and handling conditions. Avoid repeated freeze-thaw cycles. |
| Reference Data | |
| RefSeq | NP_001444 |
| Locus ID | 2296 |
| UniProt ID | Q12948, W6CJ52 |
| Cytogenetics | 6p25.3 |
| Refseq Size | 3452 |
| Refseq ORF | 1659 |
| Synonyms | ARA; ASGD3; FKHL7; FREAC-3; FREAC3; IGDA; IHG1; IRID1; RIEG3 |
| Summary | 'This gene belongs to the forkhead family of transcription factors which is characterized by a distinct DNA-binding forkhead domain. The specific function of this gene has not yet been determined; however, it has been shown to play a role in the regulation of embryonic and ocular development. Mutations in this gene cause various glaucoma phenotypes including primary congenital glaucoma, autosomal dominant iridogoniodysgenesis anomaly, and Axenfeld-Rieger anomaly. [provided by RefSeq, Jul 2008]' |
| Protein Families | Druggable Genome, Transcription Factors |
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