This gene encodes a member of the dynamin superfamily of GTPases. The encoded protein mediates mitochondrial and peroxisomal division, and is involved in developmentally regulated apoptosis and programmed necrosis. Dysfunction of this gene is implicated in several neurological disorders, including Alzheimer's disease. Mutations in this gene are associated with the autosomal dominant disorder, encephalopathy, lethal, due to defective mitochondrial and peroxisomal fission (EMPF). Alternative splicing results in multiple transcript variants encoding different isoforms.
Stoccaggio: Store at -20℃ Valid for 12 months. Avoid freeze / thaw cycles.
Isotipo: IgG,κ
Clonalità: Monoclonal;Recombinant
Clone: 2C6
Coniugazione: Unconjugated
Applicazione: WB;IHC
Diluizione: IHC 1:200-1000;WB 1:1000-5000
Simbolo target: DRP1
Ig target: DRP;DLP;DNM1L;DLP1;DRP1;DVLP;DYMPLE;EMPF;EMPF1;HDYNIV;Dnm1p/Vps1p-like protein (DVLP);dynamin 1 like;Dynamin family member proline-rich carboxyl-terminal domain less (Dymple);Dynamin-1-like protein;Dynamin-like protein;DLP1;DRP1;DVLP;DYMPLE;dynamin 1 like;EMPF;EMPF1;HDYNIV;Dnm1p/Vps1p-like protein;dnml1;Dynamin family member proline-rich carboxyl-terminal domain less;Dynamin like protein;Dynamin related protein 1;Dynamin-like protein 4;Dynamin-like protein IV;Dynamin-related protein 1;DYNIV 11;FLJ41912;VPS1
Area di ricerca:Neuroscience;Cell Biology;Signal Transduction;Metabolism;Cancer
Newsletter TEMA RICERCA
Ricevi aggiornamenti rilevanti per il tuo lavoro
Inserisci la tua e-mail e seleziona le aree di interesse per ricevere le ultime novità, approfondimenti e promozioni.