MUC18 / CD146 / MCAM (Melanoma Cell Adhesion Molecule) (rMUC18/1130), 0.2mg/mL, IgG1, Clone: [rMUC18/1130], Mouse, Monoclonal

Artikelnummer: BOT-BNUB2302-500
Artikelname: MUC18 / CD146 / MCAM (Melanoma Cell Adhesion Molecule) (rMUC18/1130), 0.2mg/mL, IgG1, Clone: [rMUC18/1130], Mouse, Monoclonal
Artikelnummer: BOT-BNUB2302-500
Hersteller Artikelnummer: BNUB2302-500
Alternativnummer: BOT-BNUB2302-500-500UL
Hersteller: Biotium
Wirt: Mouse
Kategorie: Antikörper
Applikation: IHC
Spezies Reaktivität: Human
Immunogen: Recombinant full-length human MUC18 protein
Alternative Synonym: Cell Surface Glycoprotein MUC18, Cell Surface Glycoprotein P1H12, Gicerin, Melanoma Adhesion Molecule (MCAM), Melanoma Associated Glycoprotein MUC18, Melanoma Cell Adhesion Molecule, Melanoma-associated Antigen A32, Mel-CAM, S-endo 1 Endothelial-associated Antigen, Sendo1
Mel-CAM belongs to the immunoglobulin superfamily and functions as a Ca2 -independent cell adhesion molecule. Mel-CAM expression is restricted to advanced primary and metastatic melanomas and to cell lines of the neuroectodermal lineage, but not normal melanocytes. Mel-CAM is found on 80% of advanced primary human melanomas and correlates well with development of metastatic disease.Primary antibodies are available purified, or with a selection of fluorescent CF Dyes and other labels. CF Dyes offer exceptional brightness and photostability. Note: Conjugates of blue fluorescent dyes like CF405S and CF405M are not recommended for detecting low abundance targets, because blue dyes have lower fluorescence and can give higher non-specific background than other dye colors.
Klonalität: Monoclonal
Konzentration: 0.2 mg/mL
Klon-Bezeichnung: [rMUC18/1130]
Molekulargewicht: 130 kDa
Isotyp: IgG1
UniProt: P43121
Puffer: PBS, 0.05% BSA, 0.05% azide
Quelle: Animal
Anwendungsbeschreibung: Higher concentration may be required for direct detection using primary antibody conjugates than for indirect detection with secondary antibody|Immunohistology (formalin): 0.5-1.0 ug/mL for 30 minutes at RT|Staining of formalin-fixed tissues requires boiling tissue sections in 1 mM EDTA pH 8.0 for 10-20 minutes followed by cooling at RT for 20 minutes|Optimal dilution for a specific application should be determined by user