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Anti cd31 phycoerythrin pe

Manufactured by BD
Sourced in United States

Anti-CD31-phycoerythrin (PE) is a fluorescently-labeled antibody that binds to the CD31 antigen. CD31 is a cell surface protein expressed on endothelial cells and some immune cells. The phycoerythrin (PE) fluorescent dye is conjugated to the anti-CD31 antibody, allowing for the detection and analysis of CD31-positive cells using flow cytometry or fluorescence microscopy.

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2 protocols using anti cd31 phycoerythrin pe

1

Characterization of Mesenchymal Stromal Cells

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Expression of the cell surface markers CD73, CD90 and CD105 and absence of hematopoietic markers on MSCs was determined using flow cytometry, according to the statement by the International Society for Cellular Therapy [30 (link)]. Cells were detached using Trypsin/EDTA and washed in PBS/0.05% bovine serum albumin. Antibodies used were (FITC) conjugated anti-CD86-fluorescein isothiocyanate (FITC) (cat. no. 555657), anti-HLA-DR-FITC (cat. no. 347400), anti-CD31-phycoerythrin (PE) (cat no 555446), anti-CD34-PE (cat no 348057), anti-CD73-PE (cat no 550257), anti-CD90-PE (cat no 555596), anti-CD3-peridinin chlorophyll protein(PerCP)-Cy5.5 (cat no 332771), anti-CD45-PerCPCy5.5 (cat no 332784), all from BD (San Diego, CA, USA) and anti-CD105-PE (cat no SN6), from Ancell (Bayport, MN, USA). Flow cytometry was performed on a FACScalibur, and analyzed using Cellquest software (both Becton–Dickinson). Mean fluorescence intensity (MFI) ratio was calculated by determining the MFI of the specific staining relative to the MFI of the appropriate isotype control staining.
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2

Quantification and Analysis of Microparticles

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MP quantification and analysis was performed as previously described (Jenkins et al., 2011 (link)) with minor modifications. Briefly, plasma samples were thawed and platelet-poor plasma was obtained through centrifugation. Platelet-poor plasma was then further centrifuged to obtain cell-free plasma (CFP), which was used for MP analyses. 50uL of CFP was incubated with anti-CD31-phycoerythrin (PE) and anti-CD42b-fluorescein isothiocyanate (FITC), anti-CD62E-PE or anti-CD34-FITC (BD Biosciences) for 30 minutes. Samples were then fixed with 2% paraformaldehyde and diluted with filtered PBS before flow cytometric analysis.
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