Fluorescent reporter combination optimization for flow cytometry purity of labeled Drosophila neurons
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Purity assessment of different fluorescent protein reporter combinations using R24B02-GAL4 as the distinct hemilineage driver. Cells were sorted using a BD FACSAria and then fixed on poly-lysine coated culture slides. Purity was assessed by epifluorescence using a DAPI counterstain for unlabeled neurons.
创建时间:
2018-08-04



