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Percp cy5.5 anti f4 80

Manufactured by BioLegend
Sourced in United States

PerCP-Cy5.5-anti-F4/80 is a conjugated antibody used for the identification and quantification of F4/80-expressing cells in flow cytometry applications. It consists of an anti-F4/80 antibody coupled to the PerCP-Cy5.5 fluorescent dye, which allows for the detection of F4/80-positive cells.

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2 protocols using percp cy5.5 anti f4 80

1

Profiling Immune Cell Composition in Mouse Lungs

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GFP-expressing AAV or lentiviral vectors were administrated i.n. into hACE2 K18 Tg (AAV) or SAMHD1 KO mice (lentivirus). At 3-dpi, the lungs were homogenized in ACK buffer and the cells were disaggregated by a 30-min treatment with 1.5 mg/mL collagenase and 0.1 mg/mL DNase followed by passage through a 100-μm mesh. The cells were blocked with anti-CD16/CD32 (RRID:AB_1574975) and stained with Alexa 700-anti-CD45 (RRID:AB_493715), PerCP-Cy5.5-anti-F4/80 (RRID:AB_893496), APC-Cy7-SiglecF (RRID:AB_2904295), PE-Cy7-anti-CD11c (RRID:AB_493569), PE-Cy7-anti-CD19 (RRID:AB_313655), APC-anti-CD3 (RRID:AB_2561456), Pacblue-anti-CD11b (RRID:AB_755985), PE-Cy5.5-anti-CD62L (RRID:AB_313097), APC-anti-CD14 (RRID:AB_940574) and PE-Ly6C/Ly6G (Gr1) (RRID:AB_313372) (BioLegend) and analyzed on a Beckman CytoFLEX flow cytometer using with FlowJo software. Cell types were classified as epithelial (CD45−), alveolar macrophages (CD45+, F4/80+, SiglecF+), interstitial macrophages (CD45+, F4/80+, SiglecF−), DCs (CD45+, F4/80−, CD11c+), T cells (CD45+, CD3+), B cells (CD45+, CD19+), monocytes (CD45+, CD11b+, CD14+) and neutrophils (CD45+, CD62L+, Ly6C/Ly6G+). LY-CoV1404 was obtained from discarded vials of Bebtelovimab.
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2

Multicolor Flow Cytometry Analysis

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The fluorescence-labeled monoclonal antibodies were as follows: FITC-anti-CD3, PerCp-Cy5.5-anti-CD8, APC-Cy7-anti-CD11b, PerCp-Cy5.5-anti-F4/80, APC-anti-CD4, and PE-Cy7-anti-CD45 were purchased from Biolegend (San Diego, CA, USA); FITC-anti-CD11b was from BD Biosciences (San Jose, CA, USA); and PerCp-Cy5.5-anti-F4/80 was from eBioscience (San Diego, CA, USA). MNCs were stained with the indicated antibodies as previously described37 (link). Data were collected on a FACSCalibur flow cytometer (BD Biosciences) and analyzed using FlowJo 7.6.1 (Tree Star, Ashland, OR).
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