Exact(26)
Cells were analysed using a 5 laser LSRFortessa cell analyser (BD) and data analysed using FlowJo software.
Stained cells were analysed using a FACScan cell analyser (Becton-Dickinson, Mountain View, CA, USA).
Samples were then immediately analysed on an LSRFortessa™ cell analyser, BD Biosciences.
Labelled cells were analysed on a BD LSRFortessa cell analyser.
All samples were evaluated by using a BD LSRFortessa cell analyser (BD Biosciences, San Jose, CA, USA) and analysed using BD FACSDiva software (BD Biosciences) and FlowJo version 7.6.5 software (Tree Star, Ashland, OR, USA).
The samples were analysed using a FACScan (Fluorescence-Activated Cell Analyser) flow cytometer and the Cell Quest software.
Similar(34)
Cells were analysed on a BD LSRII fluorescence-activated cell sorting analyser using fluorescence-activated cell sorting Diva software.
They were then analysed using an automated Vi-CELL cell viability analyser (Beckman Coulter, Brea, CA, USA), which has linearity approximately from 5×10to to >1 × 10 cells ml−1 (Szabo et al, 2004).
The fluorescence was detected by an IN Cell 2000 Analyser.
mtDNA nucleoids were further quantified using the IN Cell 1000 analyser (GE Healthcare Life Science, Little Chalfont, UK).
Viable cells were counted using a Vi-CELL cell viability analyser (Beckman Coulter) at 24 h intervals for 96 h.
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