Sentence examples for morphology cells were from inspiring English sources

To analyze the nuclei morphology, cells were stained with Hoechst (1/20000 in PBS) for 5 min at room temperature, followed by three PBS washes.

For morphology, cells were fixed in 2.5% v/v glutaraldehyde in 0.08 M sodium cacodylate buffer (pH 7.2), and processed as described in [49].

Since retinal cells at these early stages of development do not show definitive morphology, cells were chosen at random and the post hoc strategy described below was used to retrospectively classify the cells as RPCs, transitional cells, or postmitotic neurons.

By analysis of cell morphology (cells were spindle-shaped, sticking to the fibres), attachment (fibres were enveloped by cells and ECM), and actin filament bundles (which were orientated along the fibres), we could further substantiate these findings.

For the analysis of mitochondrial morphology, cells were kept in normal culture medium until harvested.

To observe nuclear morphology, cells were fixed and stained by Hoechst 22385.

For erythroblast morphology analysis, cells were stained with antibodies against Ter119 and CD71 as above, and with Hoechst (LifeTech) and Thiazole Orange (Sigma) for nucleic acid detection.

To preserve the cell morphology, Hela cells were fixed in PBS buffer.

Based on the size and morphology, these cells were identified as neurons.

Based on their high autofluorescence and morphology, the cells were uniformly identified as macrophages.

For cell morphology analysis, cells were submitted to immunofluorescence.