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Using a combination of a metal-based membrane stain and lectins conjugated to lanthanide-chelating polymers, we demonstrate that individual Escherichia coli cells can be differentiated based on their cell surface polysaccharides using mass cytometry.
In this study, we evaluated yeast strains based on their cell growth and ethanol production in GlcNAc medium.
We observed that in spite of variability introduced by experimental conditions and different microarray platforms, our meta-analytical approach can distinguish biologically distinct normal tissues by clustering them based on their cell of origin.
His C mutant embryos were identified in the stained samples based on their cell division arrest phenotype.
Based on their cell type 14 tumours were classified as epithelioid, 28 as mixed, and 33 as spindle cell type.
Sensor array detection DFA demonstrated the ability to discriminate samples based on their cell type for all comparisons with accuracies varying between 77% and 93%.
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Contributing factors for the antimicrobial activity enhancement of N-terminally engineered mutants of cell-penetrating apidaecins were analyzed based on their cell-penetration efficiency.
As a consequence, subsets of NK cells in mouse and human have been defined based on their cell-surface phenotype and functional properties that are shaped by environmental factors among which cytokines play a major role [1] [5].
Based on their cell-penetrating ability, calcines have been used as a non-toxic drug carrier to overcomes drug resistance in cancer therapy[ 33].
L cells were identified and purified based on their cell-specific expression of the fluorescent protein Venus, using GLU-Venus transgenic mice.
SST-Cre/ROSA26EYFP mice were used to purify D-cells by flow cytometry from epithelial digests of the gastric antrum and corpus based on their cell-specific fluorescence and low side scatter (Supplemental Figure 2).
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