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Pecy7 conjugated anti cd27

Manufactured by Beckman Coulter
Sourced in United States

PECy7-conjugated anti-CD27 is a fluorochrome-conjugated monoclonal antibody that binds to the CD27 surface antigen. CD27 is a member of the tumor necrosis factor receptor superfamily and is expressed on various immune cell types. The PECy7 fluorochrome allows for the detection and analysis of CD27-positive cells using flow cytometry.

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2 protocols using pecy7 conjugated anti cd27

1

Multicolor Flow Cytometry Staining

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Staining protocol was performed as previously described [7 ]. Briefly, ex vivo or in vitro assay’s cells were stained for surface markers with a panel of monoclonal antibodies, as follows: FITC-conjugated anti-CD3; APC-conjugated anti-CD8; PECy7-conjugated anti-CD27; ECD-conjugated anti-CD45 (all Beckman Coulter, Miami, FL, USA) in PBS containing 0.1% sodium azide (NaN3; Sigma Aldrich) and 2% fetal calf serum (Sigma Aldrich) and incubated for 20 minutes on ice. Afterwards, these samples were incubated with 20 μg/mL of 7-aminoactinomycin D (7-AAD; Sigma Aldrich) for 30 minutes at 4°C, for apoptosis evaluation, as described in elsewhere. The samples were kept on 7-AAD solution, protected from light, until the flow cytometry acquisition.
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2

Phenotypic Analysis of Human PBMC Subsets

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Fresh PBMCs were stained with the following conjugated anti-human monoclonal antibodies (mAb): fluorescein isothiocyanate (FITC)–conjugated anti-CD21, energy-coupled dye–conjugated anti-CD19, allophyocyanin (APC)–conjugated anti-IgM, and phycoerythrin (PE)–Cy7–conjugated anti-CD27 (Beckman Coulter). PBMCs were also stained with PE-conjugated anti–FCRL-1, anti–FCRL-2, anti–FCRL-3, anti–FCRL-4, and anti–FCRL-5 mAb. We prepared these mAb as described previously (31 (link)–34 (link)). All of these FCRL-specific mAb were authorized as reference antibodies for FCRL proteins 1–5 (CD307a–e) in previous international human leukocyte differentiation antigens workshops (33 (link),35 (link)). We also used PE-conjugated anti–FCRL-4 mAb (clone 413D12) from BioLegend. PE-conjugated IgG1 (Beckman Coulter) was used as an isotype control. Flow cytometry was performed on a Navios flow cytometer (Beckman Coulter) and analyzed using CXP analysis (Beckman Coulter) and FlowJo software (Tree Star).
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