Transfected Stable Cell Lines
Reliable | High-Performance | Wide Rage
Precision reporter, kinase, immune receptor, biosimilar, Cas9, and knockout stable cell lines for diverse applications.
Cat. No. : MiUTR4H-TG02765
| Cat. No. | MiUTR4H-TG02765 |
| Gene Abbr | DMD |
| Gene Name | DMD dystrophin [ Homo sapiens ] |
| Species | Human |
| Reporter | GFP |
| Promoter | CMV |
| Resistance | Kanr |
| Selection Marker | Puromycin |
| Size | 1ug |
| Vector | pLenti-UTR-GFP |
| Vector Type | Lentiviral Vector |
| Storage | -20°C for up to a year |
| Gene Name | DMD dystrophin [ Homo sapiens ] |
| Gene Symbol | DMD |
| Synonyms | BMD; CMD3B; DXS142; DXS164; DXS206; DXS230; DXS239; DXS268; DXS269; DXS270; DXS272 |
| Gene Description | dystrophin (muscular dystrophy, Duchenne and Becker types) |
| GeneID | 1756 |
| Uni ProtID | P11532 |
| mRNA Refseq | NM_004019.2 |
| Protein Refseq | NP_004010.1 |
| Chromosome Location | Xp21.2 |
| Function | actin binding; dystroglycan binding; nitric-oxide synthase binding; protein binding; structural constituent of cytoskeleton; structural constituent of muscle; structural constituent of muscle; zinc ion binding; |
| Pathway | Arrhythmogenic right ventricular cardiomyopathy, organism-specific biosystem; Arrhythmogenic right ventricular cardiomyopathy (ARVC), organism-specific biosystem; Arrhythmogenic right ventricular cardiomyopathy (ARVC), conserved biosystem; Dilated cardiomyopathy, organism-specific biosystem; Dilated cardiomyopathy, conserved biosystem; Hypertrophic cardiomyopathy (HCM), organism-specific biosystem; Hypertrophic cardiomyopathy (HCM), conserved biosystem; |
| MIM | 300377 |
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