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1 NSOM fluorescence measurements, however, are able to res
2 ical transformer probe was used in an actual NSOM measurement performing hyperspectral photoluminesce
4 n limit of confocal microscopy, both AFM and NSOM measurements of mica-supported lipid monolayers rev
5 d time-correlated single-photon counting and NSOM to obtain images of fluorescence lifetimes with hig
6 d THG is a chemically specific bulk probe in NSOM imaging by tuning the excitation source onto and of
8 of a near-field scanning optical microscope (NSOM) to simultaneously map and detect colocalized prote
9 both near-field scanning optical microscopy (NSOM) and fluorescence resonance energy transfer (FRET).
17 ensional spatial autocorrelation analysis of NSOM images that resolved patches with radii of approxim
19 pots with a spatial resolution of <100 nm or NSOM fluorescence images using fluorescence lifetime as
22 hout the need for a metal coating around the NSOM probe and should work equally well with nonwaveguid
26 report room-temperature aperture-based TPEF NSOM imaging of these NCs for the first time at 30 nm po
27 bsequent investigation of the NCs using TPEF NSOM reveals that, even when they are separated by dista
31 ous dual-color excitation and detection with NSOM provided fluorescence maps together with topography
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