SMCR7L Monoklonaler Antikörper
SMCR7L Monoklonal Antikörper für WB, IHC, IF-P, Indirect ELISA
Wirt / Isotyp
Maus / IgG2b
Getestete Reaktivität
human, Maus, Ratte
Anwendung
WB, IHC, IF-P, Indirect ELISA
Konjugation
Unkonjugiert
CloneNo.
3B3G3
Kat-Nr. : 67808-1-PBS
Synonyme
Geprüfte Anwendungen
Produktinformation
67808-1-PBS bindet in WB, IHC, IF-P, Indirect ELISA SMCR7L und zeigt Reaktivität mit human, Maus, Ratten
| Getestete Reaktivität | human, Maus, Ratte |
| Wirt / Isotyp | Maus / IgG2b |
| Klonalität | Monoklonal |
| Typ | Antikörper |
| Immunogen | SMCR7L fusion protein Ag13775 |
| Vollständiger Name | Smith-Magenis syndrome chromosome region, candidate 7-like |
| Berechnetes Molekulargewicht | 463 aa, 51 kDa |
| Beobachtetes Molekulargewicht | 48-51 kDa |
| GenBank-Zugangsnummer | BC002587 |
| Gene symbol | SMCR7L |
| Gene ID (NCBI) | 54471 |
| Konjugation | Unkonjugiert |
| Form | Liquid |
| Reinigungsmethode | Protein-A-Reinigung |
| Lagerungspuffer | PBS only |
| Lagerungsbedingungen | Store at -80°C. 20ul Größen enthalten 0,1% BSA. |
Hintergrundinformationen
Human SMCR7L gene encodes, MID51, the mitochondrial dynamic protein of 51 kDa (also called mitochondrial elongation factor 1, MIEF1). MID51 is a single-pass membrane protein anchored to the mitochondrial outer membrane and regulates mitochondrial morphology. Mitochondrial morphology is controlled by two opposing processes: fusion and fission. Elevated MID51 levels induce extensive mitochondrial fusion, whereas depletion of MID51 causes mitochondrial fragmentation. MID51 interacts with and recruits Drp1 to mitochondria, suggesting a critical role of MID51 in regulation of mitochondrial fusion-fission machinery in vertebrates.







