Desmin (DES) (NM_001927) Human Recombinant Protein
CAT#: TP710055
Recombinant protein of human desmin(DES),full length,with C-terminal flag tag, expressed in sf9 cells
View other "Desmin" proteins (6)
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CNY 4020.00
CNY 1999.00
CNY 2700.00
Specifications
| Product Data | |
| Species | Human |
| Expression Host | Sf9 |
| Expression cDNA Clone or AA Sequence |
A DNA sequence from TrueORF clone, RC205685, encoding human full-length DES
|
| Tag | C-DDK |
| Predicted MW | 54 kDa |
| Concentration | >0.05 µg/µL as determined by microplate BCA method |
| Purity | > 80% as determined by SDS-PAGE and Coomassie blue staining |
| Buffer | 50 mM Tris-HCl, pH 8.0, 150 mM NaCl, 10% glycerol |
| Note | For testing in cell culture applications, please filter before use. Note that you may experience some loss of protein during the filtration process. |
| 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_001662 |
| Locus ID | 1674 |
| UniProt ID | P17661 |
| Refseq Size | 1519 |
| Cytogenetics | 2q35 |
| Refseq ORF | 873 |
| Synonyms | CDCD3; CSM1; CSM2; LGMD1D; LGMD1E; LGMD2R |
| Summary | This gene encodes a muscle-specific class III intermediate filament. Homopolymers of this protein form a stable intracytoplasmic filamentous network connecting myofibrils to each other and to the plasma membrane. Mutations in this gene are associated with desmin-related myopathy, a familial cardiac and skeletal myopathy (CSM), and with distal myopathies. [provided by RefSeq, Jul 2008] |
| Protein Families | Druggable Genome |
| Protein Pathways | Arrhythmogenic right ventricular cardiomyopathy (ARVC), Dilated cardiomyopathy, Hypertrophic cardiomyopathy (HCM) |
Documents
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Resources
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