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.

Codice: D-AB-10190L_100μL | Marca: Elabscience | Confezionamento: 100μL

Specie: Human;Mouse;RatIsotipo: IgGConiugazione: Unconjugated

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Codice: D-AB-10190L_100μL
Marca: Elabscience
Specie target: Human;Mouse;Rat
Host: Rabbit
Concentrazione: 1 mg/mL
Link: Apri link
Stoccaggio: Store at -20℃ Valid for 12 months. Avoid freeze / thaw cycles.
Isotipo: IgG
Clonalità: Polyclonal
Coniugazione: Unconjugated
Applicazione: WB;IF
Diluizione: WB 1:500-1:1000;IF 1:50-1:200
Simbolo target: DRP1
Ig target: DLP1;dnm1l;DNM1L;Dnm1p/Vps1p-like protein;dnml1;DRP1;DVLP;Dymple;Dynamin 1 like;Dynamin family member proline-rich carboxyl-terminal domain less;Dynamin like protein;Dynamin related protein 1;Dynamin-1-like protein;Dynamin-like protein 4;Dynamin-like protein;Dynamin-like protein IV;Dynamin-related protein 1;DYNIV 11;EMPF;EMPF1;FLJ41912;HdynIV;VPS1
Area di ricerca: Cancer;Cell Biology;Metabolism;Neuroscience;Signal Transduction

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