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Our assay reveals occupancy patterns at the single-cell level.
Fig. 1 A partial transfection assay reveals EGRF-GFP and EGF uptake and co-localization.
Additionally, MTT assay reveals that the two peptides have low toxicity to human cells.
The biocompatibility assay reveals that SLNs treatment did not exhibit obvious systemic toxicity in two mouse models.
Mouse limb explant assay reveals that Sox9 expands BMP2-stimulated chondrocyte proliferating zone while Smad7 promotes BMP2-intitated hypertrophic zone of the growth plate.
An anilinonaphthalene-8-sulfonic acid uptake assay reveals two distinct modes of Escherichia coli outer membrane perturbation elicited by LL37 and LL7-27.
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Cellular viability assay revealed no cytotoxic effects.
However, TUNEL assay revealed no evidence of apoptosis.
The MTT assay revealed negligible toxicity for both the hydrazones.
The XTT assay revealed dose-dependent cytotoxicity to cancer cell lines.
The MTT assay revealed that docetaxel-loaded NLC incorporated into gel showed lower cytotoxicity than docetaxel.
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