CD146/MCAM Monoklonaler Antikörper
CD146/MCAM Monoklonal Antikörper für WB, IHC, IF/ICC, IF-P, Indirect ELISA
Wirt / Isotyp
Maus / IgG1
Getestete Reaktivität
human
Anwendung
WB, IHC, IF/ICC, IF-P, Indirect ELISA
Konjugation
Unkonjugiert
CloneNo.
4D8A9
Kat-Nr. : 66153-1-PBS
Synonyme
Geprüfte Anwendungen
Produktinformation
66153-1-PBS bindet in WB, IHC, IF/ICC, IF-P, Indirect ELISA CD146/MCAM und zeigt Reaktivität mit human
Getestete Reaktivität | human |
Wirt / Isotyp | Maus / IgG1 |
Klonalität | Monoklonal |
Typ | Antikörper |
Immunogen | CD146/MCAM fusion protein Ag11855 |
Vollständiger Name | melanoma cell adhesion molecule |
Berechnetes Molekulargewicht | 646 aa, 72 kDa |
Beobachtetes Molekulargewicht | 120 kDa |
GenBank-Zugangsnummer | BC056418 |
Gene symbol | CD146 |
Gene ID (NCBI) | 4162 |
Konjugation | Unkonjugiert |
Form | Liquid |
Reinigungsmethode | Protein-G-Reinigung |
Lagerungspuffer | PBS only |
Lagerungsbedingungen | Store at -80°C. 20ul Größen enthalten 0,1% BSA. |
Hintergrundinformationen
CD146, also known as melanoma cell adhesion molecule (MCAM) or MUC18, originally identified as a biomarker of melanoma progression, is a transmembrane glycoprotein of 113-130 kDa, belonging to the immunoglobulin (Ig) superfamily (PMID: 8378324; 25993332). Structurally, it consists of five Ig domains, a transmembrane domain, and a cytoplasmic region. In normal adult tissue, CD146 is primarily expressed by vascular endothelium and smooth muscle. CD146 is a key cell adhesion protein in vascular endothelial cell activity and angiogenesis, and has been used as marker of circulating endothelium cells (CECs) (PMID: 19356677). In addition to the membrane-anchored form of CD146, a soluble form of CD146 (sCD146, 105 kDa) has also been found in human plasma and in the supernatant of cultured human endothelial cells (PMID: 9462829; 19229070; 16374253; 14597988). This antibody detects a band at approximately 120 kDa that corresponds to the molecular weight of glycosylated CD146. Treatment of lysates of HepG2 cells and L02 cells with PNGase F, which removes oligosaccharides from N-linked glycoproteins, led to a down-shift of the detected band.