Sentence examples for microscopy imaging in from inspiring English sources

From the point of view of microscopy imaging, in addition to expectations on image quality and definition, this particularity of living bodies sets two complementary requirements on image acquisition durations: Image acquisition has to be sufficiently short to avoid blurring effects due to biological mechanisms occurring within the specimen while the image is being recorded.

Author of some 600 papers and 14 books (one of which, 4D Electron Microscopy: Imaging in Space and Time, 2010, I co-authored), Zewail has left a lasting legacy.

For atomic force microscopy imaging in liquid (Ag, AgCr), nanoparticle samples (2 μl) were diluted in NaCl buffer (48 μl, 20 mM with 50 mM HEPES, pH 6.5) and bath sonicated (Ultrawave U300, Ultrawave, Cardiff, UK) for 15 min. Samples were incubated on freshly cleaved mica for 20 min at room temperature before imaging in NaCl buffer.

The reaction product was visualised either with diaminobenzidine as a chromogenic substrate in FFPE tissue sections or with Alexa Fluor 488 goat anti-rabbit IgG secondary antibody (Molecular Probes, Invitrogen, Paisley, UK) for fluorescence microscopy imaging in cultured cells.

We also could confirm the penetration of eGFP-tetramers into the nucleus as described by fluorescent confocal microscopy in [30] which, however, contradicts the results obtained by confocal laser scanning microscopy imaging in [48].

This study provides a new approach for injection of pathogens into the tail fin, which allows combined light and electron microscopy imaging in vivo and opens new research directions for studying autophagy process related to infectious diseases.

These bifluorophoric nanosensors have a potential for application in fluorescence microscopy imaging and in-vitro assays.

This is not the case for confocal microscopy, imaging occurs in only one plane and so any data underneath a pigmented region is lost (Figure 3G H).

Junier for fruitful discussions, A. Davy for providing the BITC25 cells, P. Bellenger for the anti-TOM20 antibody, P. Cochard for the anti-Olig2 antibody and for advice in microscopy imaging and the LITC-CBD Imaging platform and B. Ronsin and S. Bosch for microscopy assistance.

MD, PM6, and ab initio simulations of dry SLG and dry and wetted SLGO and electron microscopy imaging show marked differences in the properties of the materials that can explain variations in previously observed results for the pH dependent behavior of SLGO and electrical conductivity of chemically modified graphene-polymer composites.

Advances in microscopy, imaging, and computational analyses potentially allow more detailed investigations than have previously been possible.