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Ebiocb16

Manufactured by Thermo Fisher Scientific
Sourced in United States

The EBioCB16 is a high-performance benchtop centrifuge designed for a variety of laboratory applications. It features a simple and intuitive control interface, ensuring easy operation. The centrifuge can accommodate 16 microtubes or 8 PCR strips, and provides a maximum speed of 16,000 rpm with a maximum RCF of 24,400 x g.

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3 protocols using ebiocb16

1

Multiparameter FACS Staining for Immune Profiling

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For FACS staining, we used the following antibodies to target: CD16 (FITC; eBioCB16), CD14 (PE-Cy7; 61D3), CD15 (APC; MMA), IL-4 (APC; 8D4-8), and IFN-γ (4S.B3)—all purchased from eBioscience (San Diego, CA, USA)—and CD11b (FITC; ICRF44), CD56 (PE; HCD56), CD33 (PE; WM53), IL-10 (PE; JES3-9D7) CD45 (APC; HI30), CD163 (APC; GH1/61), CD3 (PE-Cy7; HIT3a), CD4 (FITC; OKT4), and IL-17A (PE; BL168)—all purchased from BioLegend (San Diego, CA, USA).
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2

Immunophenotypic Analysis of CD16+CD177+ Neutrophils

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We performed immunophenotypic analysis using distinct fluorochrome-conjugated monoclonal antibodies that recognized human CD177 (MEM-166 clone, eBioscience), or CD16 (eBioCB16, eBioscience). Cells were examined by multicolor flow cytometry using a FACSCalibur machine (BD Biosciences), and data were analyzed using CellQuest acquisition software. The CD16+CD177+ neutrophils cells were isolated by FACS sorting on a BD FACSAria system (BD Biosciences).
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3

Immunophenotyping of Neutrophils in IgAV Patients

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Venous blood was drawn from IgAV patients and HBDs and collected into heparin-containing tubes. Whole blood immunophenotyping was performed using 7-Color Immunphenotyping kit (Miltenyi Biotec). Briefly, 100 μl of whole blood was incubated with 10 μl immunophenotyping reagent for 10 min in the dark, at 4 °C. After incubation, erythrocytes were lysed using Red Blood Lysing Solution (Miltenyi Biotec). Neutrophil phenotyping was performed in 50 μl of whole blood, incubated for 30 min at 4 °C in the dark with mouse anti-human antibodies to CD16 (conjugated to PE, clone eBioCB16, eBioscience), CD62L (conjugated to PE-Cyanine 5, clone DREG56, eBioscience), and CD11b (conjugated to APC, clone ICRF44, eBioscience). After incubation, samples were lysed, using Whole Blood Lysing Reagent Kit (Beckman Coulter). All samples were analyzed using flow cytometer MACSQuant Analyzer 10 (Miltenyi Biotec). Analysis of flow cytometry data was performed using MACSQquantify (Analysis Software version 2.8) and FlowLogic (Flow Cytometry Analysis Package, version 700.0a).
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