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Adherent cells were washed with PBS and incubated in Cell Dissociation Buffer (Thermo Fisher Scientific) for 20 min in a 37°C incubator to detach cells. After centrifugation, the cells were collected and counted. Cells were incubated either with or without Ab for 1 h on ice and then cells were washed three times in PBS. |
Cells were analyzed with an LSRFortessa flow cytometer (BD, Heidelberg, Germany) and FlowJo software (FlowJo, Ashland, OR, USA). |
Protocol tips |
Adherent cells were washed with PBS and incubated in Cell Dissociation Buffer (Thermo Fisher Scientific) for 20 min in a 37°C incubator to detach cells. After centrifugation, the cells were collected and counted. Cells were incubated either with or without Ab for 1 h on ice and then cells were washed three times in PBS. |
Downstream tips |
Cells were analyzed with an LSRFortessa flow cytometer (BD, Heidelberg, Germany) and FlowJo software (FlowJo, Ashland, OR, USA). |
Publication protocol
Adherent cells were washed with PBS and incubated in Cell Dissociation Buffer (Thermo Fisher Scientific) for 20 min in a 37°C incubator to detach cells. After centrifugation, the cells were collected and counted. Cells were incubated either with or without PE-labeled anti-CD70 antibody for 1 h on ice and then cells were washed three times in PBS. Cells were analyzed with an LSRFortessa flow cytometer (BD, Heidelberg, Germany) and FlowJo software (FlowJo, Ashland, OR, USA).
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