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Pe mouse anti human cd146

Manufactured by BD
Sourced in United Kingdom, United States

The PE Mouse Anti-Human CD146 is a laboratory detection reagent used to identify and quantify CD146-expressing cells. CD146, also known as MCAM, is a cell adhesion molecule that is expressed on endothelial cells, smooth muscle cells, and certain types of immune cells. This reagent can be used in flow cytometry and other immunoassays to detect and analyze CD146-positive cells in research samples.

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2 protocols using pe mouse anti human cd146

1

Characterization and Sorting of Tumor Spheres

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For flow cytometry analyses and cell sorting tumor spheres were dissociated as single cells, washed and incubated with the appropriate dilution of control or specific antibody. Antibodies used were V450 Mouse Anti-Human CD44 (561292), PE-Cy7 Mouse Anti-Human CD45 (557748), PE Mouse Anti- Human CD146 (550315), PE-Mouse Anti-Human CD24 (555428), FITC Mouse Anti-Human CD90 (561969), FITC-Mouse Anti-Human EpCAM (347197), APC-Mouse Anti-Human CD10 (332777), (all from BD Bioscience Bedford, Franklin Lakes, NJ) and Mouse monoclonal antibody [5D3] to Cytokeratin 8 + 18 (Abcam Cambridge,UK, 17139). After 45 min incubation, cells were washed. Analysis was performed using a FACS Canto flow cytometer (BD Biosciences). Cell Sorting was performed by FACS ARIA cytometer equipped with three lasers (488, 633, 407 nm) (BD Biosciences). All the cytofluorimetric acquisitions were analyzed by BD FACSDiva Software version 6.1.3 (BD Biosciences). For the sorting, cells were incubated with antibodies for 1 h then washed in PBS. Antibodies were used following manufacturing protocol indication for sorting experiment. TO-PRO3 (Thermo Fisher) dye was used for viability evaluation and used following manufacturing protocol indication. All the cytofluorimetric acquisitions were analyzed by BD FACSDiva Software version 6.1.3 (BD Biosciences).
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2

Flow Cytometry of Endothelial Cells

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Flow cytometric analyses were performed using fresh whole blood samples in order to obtain the greatest possible viable cell count. For the flow cytometric analysis of CD146 levels, PE mouse anti-human CD146 (BD Biosciences, San Jose, CA, USA) antibody was used. Peripheral blood cells were dyed using 7-aminoactinomycin D, fluorescent isothiocyanide-marked anti-CD31, phycoerythrin-marked anti-CD146, and PC5-marked anti-lymphocyte common antigen (CD45) antibodies.
Following erythrolysis, cells were evaluated using a FACS-Canto II flow cytometer (BD Biosciences). First, cells were grouped according to their expression of CD45. When CD45- negative cells (i.e., non-lymphocytic cells) were subgrouped according to the expression of CD31 (also known as platelet-endothelial cell adhesion molecule 1) and CD146 on the surface, three different subpopulations (CD31+/CD146+, CD31−/CD146+, and CD31+/CD146−) were obtained. The percentage of these populations was compared between the study group and the control group and within the study group. Peripheral endothelial cells were defined as cells with the CD45−/CD31+/CD146+ expression pattern.
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