MUC18 / Mucin 18 / CD146(MUC18/1130), 0.2mg/mL, Clone: [MUC18/1130], Mouse, Monoclonal

Catalog Number: BOT-BNUB1130-100
Article Name: MUC18 / Mucin 18 / CD146(MUC18/1130), 0.2mg/mL, Clone: [MUC18/1130], Mouse, Monoclonal
Biozol Catalog Number: BOT-BNUB1130-100
Supplier Catalog Number: BNUB1130-100
Alternative Catalog Number: BOT-BNUB1130-100-100UL
Manufacturer: Biotium
Host: Mouse
Category: Antikörper
Application: IHC
Species Reactivity: Human
Immunogen: Recombinant human MUC18 protein
Alternative Names: 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
The human Mel-CAM gene maps to chromosome 11q23 and encodes a trans-membrane glycoprotein, also designated MCAM, MUC 18 or CD146, that 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.
Clonality: Monoclonal
Concentration: 0.2 mg/mL
Clone Designation: [MUC18/1130]
Molecular Weight: 130 kDa
UniProt: P43121
Buffer: PBS, 0.05% BSA, 0.05% azide
Source: Animal
Application Notes: Higher concentration may be required for direct detection using primary antibody conjugates than for indirect detection with secondary antibody|Immunohistology (formalin)|Staining of formalin-fixed tissues requires boiling tissue sections in 10 mM Tris with 1 mM EDTA, pH 9.0, for 10-20 min followed by cooling at RT for 20 minutes|Flow Cytometry 0.5-1 ug/million cells/0.1 mL|Immunofluorescence 0.5-1.0 ug/mL|Optimal dilution for a specific application should be determined by user