Sentence examples for microscopy of primary from inspiring English sources

Phase contrast microscopy of primary naïve T cells on a PEG-coated dish confined under an agarose block.

Phase contrast microscopy of primary naïve T cells migrating on 2 µg/mL ICAM-1-coated dish under an agarose block.

Interference reflection microscopy of primary naïve T cells confined under an agarose block on PEG or ICAM-1-coated glass slide.

To assess the effect of ISR activation of C9RAN in neurons, we utilized automated fluorescent microscopy of primary rat cortical neurons co-transfected with GFP or (G4C2)×66-GFP (a reporter containing 66 G4C2 repeats in the GP reading frame just upstream of GFP) and mApple, a red fluorescent marker used to facilitate longitudinal tracking.

Quantitative time-lapse microscopy of primary human fibroblasts exposed to exogenous physiological matrix metalloproteinase (MMP) inhibitors revealed that 3-D migration is dependent on cell seeding density and occurred via highly localized MMP- and tissue inhibitor of metalloproteinases-2-dependent processes.

In this study, we used cell adhesion assays and confocal microscopy of primary murine osteoblasts and human osteoblast cell lines MG-63 and Saos-2 to demonstrate that a streptococcal collagen-like protein engineered to display the α1 and α2 integrin recognition sequences enhances osteoblast adhesion and spreading on titanium fixtures.

Scanning electron microscopy images of primary murine chondrocytes encapsulated within the matrix revealed attachment of cells onto the hydrogel matrix.

Quantitative analysis of vesicle exocytosis and classification of different modes of vesicle fusion from the fluorescence microscopy are of primary importance for biomedical researches.

For instance, scanning electron microscopy (SEM) is of primary importance to detect the formation of microstructures and detect their chemical composition.

We analysed GFP-expression by fluorescence microscopy of parasites of primary transfection populations P1 and P2 that were obtained by transfection with the donor and helper plasmid.

As shown by high-magnification microscopy of a representative primary LNCaP/GFP tumor, castration induced a dramatic decrease in tumor volume and mass (Fig. 2A and B) within 7 days of treatment compared to sham-treated animals.