Desmin (DES) Mouse Monoclonal Antibody [Clone ID: OTI14E7]
CAT#: CF814330
Carrier-free (BSA/glycerol-free) Desmin mouse monoclonal antibody, clone OTI14E7
Frequently bought together (2)
Other products for "Desmin"
Specifications
| Product Data | |
| Clone Name | OTI14E7 |
| Applications | IHC |
| Recommended Dilution | IHC 1:1000 |
| Reactivities | Human, Mouse, Rat |
| Host | Mouse |
| Isotype | IgG1 |
| Clonality | Monoclonal |
| Immunogen | Synthetic peptide (the amino acid sequence is considered to be commercially sensitive) within Human Desmin (NP_001918). The exact sequence is proprietary. |
| Formulation | Lyophilized powder (original buffer 1X PBS, pH 7.3, 8% trehalose) |
| Reconstitution Method | For reconstitution, we recommend adding 100uL distilled water to a final antibody concentration of about 1 mg/mL. To use this carrier-free antibody for conjugation experiment, we strongly recommend performing another round of desalting process. (OriGene recommends Zeba Spin Desalting Columns, 7KMWCO from Thermo Scientific) |
| Purification | Purified from mouse ascites fluids or tissue culture supernatant by affinity chromatography (protein A/G) |
| Conjugation | Unconjugated |
| Storage | Shipped at -20°C or with ice packs, Upon delivery store at -20°C. Dilute in PBS(pH7.3) if necessary. Stable for 12 months from date of receipt. Avoid repeated freeze-thaws. |
| Stability | Stable for 12 months from date of receipt. |
| Predicted Protein Size | 53.5 kDa |
| Gene Name | desmin |
| Database Link | |
| Background | 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] |
| Synonyms | CDCD3; CSM1; CSM2; LGMD1D; LGMD1E; LGMD2R |
| Reference Data | |
| Protein Families | Druggable Genome |
| Protein Pathways | Arrhythmogenic right ventricular cardiomyopathy (ARVC), Dilated cardiomyopathy, Hypertrophic cardiomyopathy (HCM) |
Documents
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