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1 TIRFM also increased in response to Gd3+, a competitive
2 TIRFM and biotinylation assays show robust receptor- and
3 TIRFM data were confirmed in human DAT-N2A cells using b
4 TIRFM images were acquired by a cooled CCD camera in app
6 his study, we report the implementation of a TIRFM-based polarization technique to detect rapid submi
9 ructed for computer-automated multiple angle-TIRFM (MA-TIRFM) using a right angle F2 glass prism (n(r
12 scope, the stage of which was configured for TIRFM imaging of fluorescently labeled human umbilical v
13 parameter, are automatically estimated from TIRFM image sequences, to account for both the lateral d
17 Live observation of fibrin polymerization in TIRFM by diffusive mixing of thrombin and plasma reveale
18 ocus drift compensation, a common problem in TIRFM due to the narrow excitation depth, particularly w
19 aser light, the typical excitation source in TIRFM, often creates spatial interference fringes across
22 ica lens (458 mm radius, n(r) 1.463); the MA-TIRFM map accurately reproduced the lens spherical surfa
23 computer-automated multiple angle-TIRFM (MA-TIRFM) using a right angle F2 glass prism (n(r) 1.632) t
24 internal reflection fluorescence microscope (TIRFM) was constructed and tested for the highest vertic
25 internal reflection fluorescence microscope (TIRFM) was used for optical imaging of exocytosis and su
26 internal reflection fluorescence microscopy (TIRFM) achieves subdiffraction axial sectioning by confi
27 internal reflection fluorescence microscopy (TIRFM) and kinetic and thermodynamic measurements, we es
28 internal reflection fluorescence microscopy (TIRFM) and spatial statistics, we observed that lysosoma
29 internal reflection fluorescence microscopy (TIRFM) and wide-field imaging of live cells to analyze t
30 internal reflection fluorescence microscopy (TIRFM) for high resolution imaging and molecular transpo
31 internal reflection fluorescence microscopy (TIRFM) from the apical side, allowed us to visualize the
32 internal reflection fluorescence microscopy (TIRFM) has joined confocal microscopy as a complementary
34 internal reflection fluorescence microscopy (TIRFM) images the plasma membrane-cytosol interface and
35 internal reflection fluorescence microscopy (TIRFM) is becoming an increasingly common methodology to
36 nternal reflectance fluorescence microscopy (TIRFM) is reported that allows quantification of the pen
37 internal reflection fluorescence microscopy (TIRFM) is the method of choice to visualize a variety of
38 internal reflection fluorescence microscopy (TIRFM) is well suited to focus on the late steps of exoc
39 internal reflection fluorescence microscopy (TIRFM) studies suggest that some LDCVs, although being a
40 internal reflection fluorescence microscopy (TIRFM) to examine the transmission of force from the api
41 internal reflection fluorescence microscopy (TIRFM) to investigate the characteristics of the yeast h
42 internal reflection fluorescence microscopy (TIRFM) to visualize the spatial-temporal recruitment of
43 internal reflection fluorescence microscopy (TIRFM) to visualize vesicular fusion events in astrocyte
45 internal reflection fluorescence microscopy (TIRFM), combined with single particle tracking, to probe
46 internal reflection fluorescence microscopy (TIRFM), custom software-based detection, and selective p
47 internal reflection fluorescence microscopy (TIRFM), the dynamics of bovine serum albumin (BSA) and h
48 internal reflection fluorescence microscopy (TIRFM), these "molecular curtains" allow for the direct
49 internal reflection fluorescence microscopy (TIRFM), we monitored green fluorescent protein-labeled T
57 internal reflection fluorescent microscopy (TIRFM) to image DRD2 with a superecliptic pHluorin tagge
59 is study shows that in vitro single-molecule TIRFM provides a new window into the molecular mechanism
62 ine adrenal chromaffin cells using polarized TIRFM demonstrate rapid and varied submicrometer changes
63 e find that azimuthal beam spinning produces TIRFM images that more accurately portray the real fluor
67 internalize particular GPCRs, we adapted the TIRFM imaging assay to simultaneously quantify the inter
68 to minimize these fringes by modulating the TIRFM field during a frame capture period; however, thes
71 Data presented here from real-time TIRF (TIRFM) and confocal microscopy coupled with surface biot