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MGP Monoklonaler Antikörper
MGP Monoklonal Antikörper für WB, IHC, IF-P, Indirect ELISA
Wirt / Isotyp
Maus / IgG2a
Getestete Reaktivität
human, Maus
Anwendung
WB, IHC, IF-P, Indirect ELISA
Konjugation
Unkonjugiert
CloneNo.
1A1C3
Kat-Nr. : 60055-1-PBS
Synonyme
Geprüfte Anwendungen
Produktinformation
60055-1-PBS bindet in WB, IHC, IF-P, Indirect ELISA MGP und zeigt Reaktivität mit human, Maus
| Getestete Reaktivität | human, Maus |
| Wirt / Isotyp | Maus / IgG2a |
| Klonalität | Monoklonal |
| Typ | Antikörper |
| Immunogen | MGP fusion protein Ag1091 |
| Vollständiger Name | matrix Gla protein |
| Berechnetes Molekulargewicht | 103 aa, 13 kDa |
| Beobachtetes Molekulargewicht | 12 kDa |
| GenBank-Zugangsnummer | BC005272 |
| Gene symbol | MGP |
| Gene ID (NCBI) | 4256 |
| Konjugation | Unkonjugiert |
| Form | Liquid |
| Reinigungsmethode | Protein-A-Reinigung |
| Lagerungspuffer | PBS only |
| Lagerungsbedingungen | Store at -80°C. 20ul Größen enthalten 0,1% BSA. |
Hintergrundinformationen
Matrix Gla protein (MGP) is is a vitamin K-dependent, extracellular matrix protein. MGP plays a pivotal role in preventing soft tissue calcification and local mineralization of the vascular wall. Vitamin K deficiency leads to inactive uncarboxylated MGP (ucMGP), which accumulates at sites of arterial calcification. However MGP is synthesized in many tissues and is especially enriched in embryonic tissues and in cancer cells. Defects in MGP are the cause of Keutel syndrome (KS), which is an autosomal recessive disorder characterized by abnormal cartilage calcification, peripheral pulmonary stenosis neural hearing loss and midfacial hypoplasia.







































