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

dJ1104E15.3, FLJ20232, HSU79252, MID51, MIEF1, SMCR7L



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 Molekulargewicht48-51 kDa
GenBank-ZugangsnummerBC002587
Gene symbol SMCR7L
Gene ID (NCBI) 54471
Konjugation Unkonjugiert
Form Liquid
Reinigungsmethode Protein-A-Reinigung
Lagerungspuffer PBS only
LagerungsbedingungenStore 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.