DRP1 (Phospho Ser616) Rabbit Monoclonal Antibody
Various whole cell lysates were separated by 4-20% SDS-PAGE, and the primary antibody was used at 4℃, over night with a 1:5000 dilution. Lane1: Jurkat - Human acute T cell leukemia cells Lane2: MCF7 - Human breast cancer Lane3: SH-SY5Y - Human neuroblastoma cells Lane4: NIH-3T3 - NIH mouse fibroblasts Lane5: RAW264.7 - Mouse mononuclear macrophage leukemia cells Lane6: C6 - Rat glioma cells Lane7: PC-12 - Pheochromocytoma in rats Predicted band size: 82kDa Observed band size: 82kDa
| Catalog Number: | MABN36671 |
| Conjugate: | Unconjugated |
| Size: | 100 ul |
| Concentration: | 1mg/ml |
| Host: | Rabbit |
| Isotype: | IgG,Kappa |
| Reactivity: | Human,Mouse,Rat |
| Applications: | WB 1:2000-1:10000;IF 1:200-1:1000;ELISA 1:5000-1:20000;IP 1:50-1:200 |
| Molecular Weight: | Observed MW:82kDa |
| Purification: | Protein A |
| Form: | Liquid |
| Synonyms: | DNM1L;DLP1;DRP1;Dynamin-1-like protein;Dnm1p/Vps1p-like protein;DVLP;Dynamin family member proline-rich carboxyl-terminal domain less;Dymple;Dynamin-like protein;Dynamin-like protein 4;Dynamin-like protein IV;HdynIV;Dynamin-related |
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. [provided by RefSeq, Jun 2013]
Applications
WB 1:2000-1:10000;IF 1:200-1:1000;ELISA 1:5000-1:20000;IP 1:50-1:200
