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1              Cell morphology was assessed by fluorescent staining.
2  debridement was monitored and visualized by fluorescent staining.
3 and heterochromatin was compared to standard fluorescent staining.
4 ty was assessed with confocal microscopy and fluorescent staining.
5  based on high and homogeneous expression on fluorescent staining.
6                                Combinatorial fluorescent staining allows simultaneous analysis of seq
7                   Additionally, we performed fluorescent staining and confocal microscopy on each gla
8 adiolabeling and scintillation counting with fluorescent staining and digital imaging.
9 123 AA patients, using intracellular 2-color fluorescent staining and flow cytometry.
10                                              Fluorescent staining and gene expression profiling of sp
11                                 By combining fluorescent staining and microspectroscopy with software
12 rved at the mineralization front using vital fluorescent staining and SEM.
13  validate their close localization by immuno-fluorescent staining and spatial transcriptomics.
14 with the use of 4,6-diamidino-2-phenylindole-fluorescent staining, and by decreases in the sensitivit
15 s assessed by electron microscopy, annexin V fluorescent staining, and flow-cytometric terminal deoxy
16 ll staining including cell permeabilization, fluorescent staining, and molecular delivery to viable c
17 ned by using confocal microscopy of multiple fluorescent stainings at the arterial level, and by usin
18                                        Using fluorescent staining, confocal microscopy and 3D reconst
19 nt fluorophore labeling by the addition of a fluorescent staining dye to the sample proteins either d
20                  Using combined Wet-SEEC and fluorescent-staining experiments, we observed slime depo
21              These results were confirmed by fluorescent staining, flow cytometry, and scanning elect
22 ssue using whole-mount click chemistry-based fluorescent staining followed by light sheet fluorescent
23 l staining for alpha-smooth muscle actin and fluorescent staining for fibrillar actin.
24                                              Fluorescent staining has previously been used to image l
25 sional electrophoresis (2-DE), visualized by fluorescent staining, imaged, and analyzed as a function
26 neck decreased, and most of the sperm showed fluorescent staining in the anterior head.
27             Immunolocalization of VCP showed fluorescent staining in the neck of noncapacitated sperm
28 f these 3D images, which exhibited irregular fluorescent staining, low autofluorescence signal or het
29 el sensitive approach which combines in situ fluorescent staining of accumulated decellularised ECM p
30 n enzyme-linked immunosorbent assay based on fluorescent staining of C. albicans with calcoflour.
31 science and biomedical applications, such as fluorescent staining of DNA and proteins in gel electrop
32                                          The fluorescent staining of encapsulated nucleic acids was p
33 sue with subsequent immunohistochemistry and fluorescent staining of histological features.
34  found, using Yop beta-lactamase hybrids and fluorescent staining of live cells from plague-infected
35  several signaling pathways, cytometry after fluorescent staining of markers with antibodies does not
36                            In control cells, fluorescent staining of neutral lipids with Bodipy 493/5
37 gene was disrupted, based on phosphospecific fluorescent staining of proteins separated by 2-dimensio
38  coincided with t-tubules as visualized with fluorescent staining of the cell membrane.
39 oticed that the MreB cytoskeleton influences fluorescent staining of the cytoplasmic membrane.
40                                       Immuno-fluorescent staining of the debrided tissues using a spe
41 toxic fluorescent marker allowing a specific fluorescent staining of the human colonic mucus.
42 ematically evaluated by in vitro and in situ fluorescent staining of the spinal cord and the brain, a
43                                    By direct fluorescent staining of uncultured spirochetes ex vivo a
44                                              Fluorescent staining of virus-like particles purified fr
45  to examine differences in the proportion of fluorescent staining on the general surface membrane com
46 l proteins and displayed a punctate speckled fluorescent staining pattern.
47                We have developed several new fluorescent staining procedures that enabled us to study
48          Viability of E325 was monitored via fluorescent staining, revealing either lack of or minima
49 ts, unique surface morphological traits, and fluorescent staining to identify microfibers in environm
50 diverse suite of molecular tools and in situ fluorescent staining to target different levels of subce
51 in environmental samples, based on selective fluorescent staining using Nile Red (NR), followed by de
52                               Double-labeled fluorescent staining was used to examine the cellular lo
53 tary techniques such as Western blotting and fluorescent staining, we confirmed the differential expr
54                                        Using fluorescent staining, we correlate the observed cell beh
55                                 Using double-fluorescent staining, we localized tac3a-expressing cell
56 netic column-purified CD42(+) MK and 2-color fluorescent staining with antibodies directed against CD
57                         Methods of selective fluorescent staining with confocal laser scanning micros
58 d to induce apoptosis in DCs as indicated by fluorescent staining with FITC-VAD-FMK.
59 of the FKBP12(F36V) fusion, and the level of fluorescent staining with FL-SLF' was proportional to th
60                                              Fluorescent staining with Nile red dye has proven to be
61 phology of apoptotic cells was visualized by fluorescent staining with propidium iodide.