FOXL2 Mutant (C134W) Human Recombinant Protein
CAT#: TP701127
Purified mutant recombinant protein of Human forkhead box L2 (FOXL2), mutation at(C134W)
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CNY 7110.00
货期*
4周
规格
Specifications
| Product Data | |
| Description | Purified mutant recombinant protein of Human forkhead box L2 (FOXL2), mutation at(C134W) |
| Species | Human |
| Expression Host | HEK293T |
| Expression cDNA Clone or AA Sequence | A DNA sequence from TrueORF clone, RC209127, encoding the full-length of FOXL2(C134W) |
| Tag | Myc-DDK |
| Predicted MW | 38.6 kDa |
| Concentration | >0.05 µg/µL as determined by microplate Bradford method |
| Purity | > 80% as determined by SDS-PAGE and Coomassie blue staining |
| Buffer | 25 mM Tris-HCl, 100 mM glycine, pH 7.3, 10% glycerol |
| Note | For culture applications, please filter before use. Note that you may experience some loss of protein during the filtration process. |
| Storage | Store at -80°C after receiving vials. |
| Stability | Stable for at least 12 months from receipt of products under proper storage and handling conditions. Avoid repeated freeze-thaw cycles. |
| Reference Data | |
| RefSeq | NP_075555.1 |
| Locus ID | 668 |
| Refseq Size | 2744 |
| Cytogenetics | 3q22.3 |
| Refseq ORF | 1128 |
| Synonyms | BPES; BPES1; PFRK; PINTO; POF3 |
| Summary | This gene encodes a forkhead transcription factor. The protein contains a fork-head DNA-binding domain and may play a role in ovarian development and function. Expansion of a polyalanine repeat region and other mutations in this gene are a cause of blepharophimosis syndrome and premature ovarian failure 3. [provided by RefSeq, Jul 2016] |
| Protein Families | Druggable Genome, Transcription Factors |
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