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1 tion was analyzed by confocal microscopy and spectrofluorometry.
2 lular Ca(2+) concentrations were measured by spectrofluorometry.
3 ve dye fura-2 to monitor [Ca(2+)](i) by bulk spectrofluorometry.
4 goxigenin nick-end labeling and quantitative spectrofluorometry.
5 ifts of NADH were measured by rapid scanning spectrofluorometry.
6 (pyranine), in combination with stopped-flow spectrofluorometry.
7  sample-tissue DNA content was measured with spectrofluorometry.
8 nd displacement were studied by stopped-flow spectrofluorometry.
9 nd by nuclear magnetic resonance spectra and spectrofluorometry.
10 ntent of each dextran type was determined by spectrofluorometry.
11                                 Stopped flow spectrofluorometry analysis of recombinant HEK293 cells
12                       Using a combination of spectrofluorometry and flow cytometry experiments, we fo
13 ted of TL were applied over the corneas, and spectrofluorometry and fluorescent stereomicroscopy were
14                                        Using spectrofluorometry and laser confocal microscopy, the ab
15 otein (RBP) and transthyretin was studied by spectrofluorometry and size-exclusion chromatography.
16 actility were measured using dual excitation spectrofluorometry and video-edge detection system (Iono
17                            Using single cell spectrofluorometry and whole-cell patch clamping, we sho
18 ia quartz crystal microbalance, sand column, spectrofluorometry, and dynamic light scattering techniq
19 on and permeability by protease sensitivity, spectrofluorometry, and negative staining electron micro
20 o quantitate intracellular Ca2+ ([Ca2+]i) by spectrofluorometry, and uPAR was aggregated by Ab cross-
21 tracellular Ca2+ concentrations ([Ca2+]i) by spectrofluorometry, and uPAR was aggregated by mAb cross
22                 UV-vis spectrophotometry and spectrofluorometry are indispensable tools in education,
23                                 Stopped-flow spectrofluorometry, combined with presteady-state kineti
24 alogue with membrane vesicles was studied by spectrofluorometry, Congo Red binding, and electron micr
25 ellular calcium handling, measured by Rhod 2 spectrofluorometry, demonstrated lower diastolic calcium
26 uorescein fluorescence by flow cytometry and spectrofluorometry, electrophoretic mobility shift assay
27  xXPA for ds undamaged DNA determined in our spectrofluorometry experiments was up to 3 orders of mag
28 the oxidation of 2',7'-dichlorofluorescin by spectrofluorometry, flow cytometry, and confocal microsc
29 (BSA) was investigated by spectrophotometry, spectrofluorometry, FT-IR and circular dichroism (CD) te
30  (Fl-) PEDF and ovalbumin were determined by spectrofluorometry, laser scanning, immunoblotting, epif
31   Rapid mix/chemical quench and stopped-flow spectrofluorometry measurements were carried out with Rh
32                      Confocal microscopy and spectrofluorometry of HER2-overexpressing breast cancer
33 ction systems based on spectrophotometry and spectrofluorometry principles, customizing laboratory de
34 y to examine secretion of catecholamines and spectrofluorometry to measure cytosolic Ca.
35 plasts was directly measured by stopped-flow spectrofluorometry using membrane vesicles loaded with t
36 plasts was directly measured by stopped-flow spectrofluorometry using membrane vesicles loaded with t
37 plasts was directly measured by stopped-flow spectrofluorometry using membranes loaded with the Cu(2+
38 acellular calcium [Ca2+]i measured by rhod-2 spectrofluorometry was increased in dopamine-reperfused
39                                              Spectrofluorometry was used to analyze thiobarbituric ac
40 ermal titration calorimetry and stopped-flow spectrofluorometry, we directly examined metal binding t
41                Using confocal microscopy and spectrofluorometry, we found that LPS was rapidly intern
42                                Second, using spectrofluorometry, we quantified the release of dye lib