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1 ivated myosins attach filaments to the glass coverslip.
2 apped and levitated above the surface of the coverslip.
3 tically trapped in solution and adhered to a coverslip.
4 ed to nitrocellulose-coated glass beads on a coverslip.
5  avoiding fluorescence interference from the coverslip.
6 of inner from outer retinal cells across the coverslip.
7 er or exhibited serpentine gliding along the coverslip.
8  the contact area formed by the bead and the coverslip.
9 arose bead resting on a functionalized glass coverslip.
10 ar or parallel to the plane of the substrate coverslip.
11 y was dependent on the myosin density on the coverslip.
12 ection of flow during myosin adhesion to the coverslip.
13 hrough the surface of a rice leaf or plastic coverslip.
14 e mainly oriented in a flat alignment on the coverslip.
15  resolution over a range of 800 nm above the coverslip.
16 erned atomic-force microscope cantilever and coverslip.
17 ng to the surface of a biotin-modified glass coverslip.
18 res germinating when adhered on a microscope coverslip.
19 med between a plano-convex lens and a planar coverslip.
20 de from titanium and incorporates a standard coverslip.
21 and reperfusion was mimicked by removing the coverslip.
22 oresist on a chemically functionalized glass coverslip.
23 omparison with photobleaching on an uncoated coverslip.
24 olecules located where the cell contacts the coverslip.
25 roelectrodes were microfabricated on a glass coverslip.
26 ring fibroblast spreading on collagen-coated coverslips.
27 d supported membranes on silica beads and on coverslips.
28  rabbit retina grown on laminin-coated glass coverslips.
29 -37 were dissected out and cultured on glass coverslips.
30 y available microprisms attached to standard coverslips.
31 in unpolarized osteoclasts cultured on glass coverslips.
32 samples are prepared conventionally on glass coverslips.
33 it flat lamellipodia on poly-L-lysine-coated coverslips.
34  20 arrays of gold nanostructures atop glass coverslips.
35 20-fold more slowly than the sample on glass coverslips.
36 rs tethered to the surface of functionalized coverslips.
37 ter 45 min of acetone fixation of shell vial coverslips.
38 f a convex lens is used to deform a flexible coverslip above a substrate containing embedded nanotopo
39 ing blebbistatin to the cells or use of soft coverslips, also formed microtubule-dependent dendritic
40  footprint (surface area in contact with the coverslip), an effect previously attributed to exocytic
41    Approximately 25,000 RGCs were seeded per coverslip and cultured for 3 days before testing.
42 n allow a particle to be moved away from the coverslip and into solution, avoiding fluorescence inter
43 lecule localization microscopy away from the coverslip and into thicker specimens will greatly broade
44 s from steric hindrances from the microscope coverslip and other surface effects.
45 tro when plated onto a localized region of a coverslip and overlaid with neonatal rat ventricular myo
46 an array within a thin film of aluminum on a coverslip and planarized to achieve no height distinctio
47  events at the contact point between a glass coverslip and the plasma membrane.
48 formation at the interface between the glass coverslip and the polymer micropallet.
49 ess when the distance between the microscope coverslip and the trap focus is being changed.
50 s and fixed before centrifugation onto glass coverslips and air drying.
51 operties to a variety of substrates, such as coverslips and Eppendorf tubes.
52 minate combustible materials such as plastic coverslips and grease.
53            Fixed yeast cells are attached to coverslips and hybridized with a mixture of FISH probes,
54 ith a mixture of smFISH probes, mounted onto coverslips and imaged in 3D.
55 vine serum albumin and were dried onto glass coverslips and kept at different relative humidities.
56  in intracellular pH (pHi) in cells grown on coverslips and loaded with 2',7'-bis(2-carboxyethyl)-5(6
57                Mitochondria were attached to coverslips and perfused with K+-based buffer containing
58 m marked the location of cultured neurons on coverslips and provided unequivocal relocation of ATP-re
59                Mitochondria were attached to coverslips and superfused with K(+)-based HEPES-buffer m
60  Chinese hamster ovary cells were adhered to coverslips and then allowed to bind labeled microtubules
61                    BCECs were grown on glass coverslips and then perfused with HCO(3)(-)-free Ringer'
62 he central portion of monolayer with a glass coverslip, and reperfusion was mimicked by removing the
63 cles that are attached to the surface of the coverslip, and the sensitivity and selectivity of detect
64 , cells were passaged onto rectangular glass coverslips, and anisotonically induced volume changes we
65 cells were isolated from rat lens, plated on coverslips, and placed in a temperature-controlled chamb
66 lls tethered by a single flagellum to quartz coverslips; and 3). the motor response time of individua
67 croscopy (OSAM) technique which can search a coverslip area of 50 x 24 mm(2) in just 5.3 min and loca
68 eeks in advance, and it takes 5 d to prepare coverslips as a substrate for neuronal growth.
69 hoeae forms a biofilm in flow cells on glass coverslips as well as on primary cervical epithelial cel
70 lens fiber cells were isolated and plated on coverslips at the bottom of a temperature-controlled cha
71  heavy chain attached to streptavidin-coated coverslips at various surface densities.
72                                              Coverslip-attached cells were perfused in an imaging cha
73                                   Individual coverslip-attached fibroblasts were loaded with the calc
74 stomer, polydimethylsiloxane on a microscope coverslip base.
75  to a fluid inlet, a circular portion of the coverslip beneath the well exploded outward but very lit
76 chia coli was tethered covalently to a glass coverslip by a single flagellum, and its rotation was st
77 of Escherichia coli were tethered to a glass coverslip by means of a single flagellum: such cells rot
78 bacterium Escherichia coli tethered to glass coverslips by single flagella.
79 abilized grids or poly-L-lysine-coated glass coverslips by transmission electron microscopy or immuno
80 was routinely cultured and seeded onto glass coverslips (c-met immunodetection), 12-well plates (DNA
81 ers and focal adhesions) typical of cells on coverslips, cells spread with lamellipodial extensions a
82 it from the close approximation of slide and coverslip ("chimneying").
83 cle is fluorescently labeled and placed on a coverslip coated with a thin layer of noble metal.
84 g of a nonadhesive agar (agarose) onto glass coverslips coated with a cell adhesive film (poly(L-lysi
85 s of activated T cells, we plated T cells on coverslips coated with antibodies to the T cell receptor
86 npermissive clone 17 (minus) was adherent to coverslips coated with chemokines, was phagocytic, kille
87 e objective (1.65) and high-refractive-index coverslips coated with gold, it is possible to follow ro
88 ed blood eosinophils were incubated on glass coverslips coated with intravenous immunoglobulin and in
89 cytes plated on uncoated coverslips (LMN) or coverslips coated with LMN (+LMN).
90 damage can be achieved by imaging samples on coverslips coated with monolayers of silver nanoparticle
91 and protein L-antibody interactions on glass coverslips coated with polyethylene glycol.
92 molecules of actin of a myofibril on Olympus coverslips coated with SIF decreased at least 30-fold in
93 lightly with rhodamine-phalloidin, placed on coverslips coated with SIF, illuminated by total interna
94 easured fluorescence from a sample placed on coverslips coated with silver island films (SIF).
95                 Within seconds of contacting coverslips coated with stimulatory antibodies, T cells d
96  HLE on the cell surface and was adherent to coverslips coated with the HLECS ligands alpha1proteinas
97 titate CLAN formation in HTM cells plated on coverslips coated with various extracellular matrix (ECM
98 cked by areas where the MT was anchored to a coverslip, consistent with a coupling structure encircli
99  by hrpA mutants for 48 h on collagen-coated coverslips demonstrated significant reductions compared
100 acilitates DNA loading, stretching and glass coverslip deposition from microliter-scale DNA samples.
101     Cells were grown at low density on glass coverslips, encased in a flow-through chamber, and conti
102 lity assays, co-sedimentation assays, and on-coverslip enzyme-linked immunosorbent assays to quantify
103  in RPMI 1640 with 10% fetal bovine serum on coverslips for 8 days or assayed for colony-forming effi
104 ree medium for approximately 2 days on glass coverslips for subsequent patch-clamp studies employing
105 d preparation of nanofibers aligned on glass coverslips for the study of membrane wrapping by rodent
106 dipocytes, grown and differentiated on glass coverslips, for at least 2 h.
107 dendritic extensions, whereas fibroblasts on coverslips formed lamellipodial extensions and were spre
108 flux from HRP-catalyzed assays on disposable coverslips functionalized with HRP and placed proximal t
109                                        Glass coverslips gave no response under all experimental condi
110                      In cells grown on glass coverslips, GFP-CFTR was polarized to the basolateral me
111 er dye washout and tested our method on both coverslip-grown cell clusters and filter-grown intact mo
112 ent support substrates: (i) microscope slide coverslips; (ii) Al foil; and (iii) Cu tapes.
113 of Listeria moving between a glass-slide and coverslip in a Xenopus frog egg extract motility assay.
114 ts and cultured on polylysine/laminin-coated coverslips in serum-free medium for 2 days.
115 film formation on human gallstones and glass coverslips in vitro, including confocal, light, and scan
116 ime to virtually any cell type attached to a coverslip, independently of cellular shape and geometry.
117 e modelled as in vitro "microcosms" on glass coverslips inoculated with the natural microbial populat
118 in volumes comparable to those used by glass coverslips is presented.
119 and well-spread primary islet cells on glass coverslips is required for detailed imaging studies by s
120                                       During coverslip ischemia, action potential duration shortened,
121    Because the PDMS chambers are bonded to a coverslip, it is possible to image P. patens development
122  isolated atrial myocytes plated on uncoated coverslips (LMN) or coverslips coated with LMN (+LMN).
123                   Calu-3 cells were grown on coverslips, loaded with the pH-sensitive fluorescent dye
124  pattern totally internally reflected at the coverslip-medium interface which excites fluorescence on
125  HepG2 cells were cultured in pairs on glass coverslips micropatterned with polyethylene glycol disil
126 r observed for enterocyte migration on glass coverslips, namely the dependence of migration speed on
127                                              Coverslips of cultured human coronary artery ECs were pl
128 ished as monolayers on glass collagen-coated coverslips or on semipermeable membranes at an air-fluid
129 old and tenfold, respectively, compared with coverslips or rigid PMAs.
130 wild-type and fap1 mutant strains on plastic coverslips over time.
131       Compared with cells on collagen-coated coverslips, phagocytosis of fibronectin-coated beads by
132 ile the physical sweeping step using a glass coverslip removes the excess cells outside the microwell
133 ques, and surface blotting of plaques onto a coverslip, revealed that fluorescent puncta were probabl
134  cells plated on extracellular matrix-coated coverslips showed enhanced invadopodia formation in resp
135 ol should take 1 h 30 min including time for coverslipping slides.
136 5 mM were observed in neurones on 27% of the coverslips studied.
137 ing and astrocytes or BON cells grown on the coverslip surface modify the dark-field signal.
138 n optically trapped bead in contact with the coverslip surface while observing the bead's thermal mot
139 tethering either DNA or PcrA to a microscope coverslip surface, unwinding of both linear and natural
140 , AtKCBP no longer binds microtubules to the coverslip surface.
141 ly) at depths approximately 250 mum from the coverslip surface.
142 ergistic combination of vacuum degassing and coverslip sweeping.
143                 In a myocyte lying flat on a coverslip, t-tubules typically progressed from its upper
144               Fibroblasts on collagen-coated coverslips that were unable to develop stress fibers and
145 rface membrane in close contact with a glass coverslip (the "footprint").
146                    For vesicles adhered to a coverslip, the confocal probe can be scanned through the
147                         Immobilized on glass coverslips, the thin-film MIPs of 1 displayed a clear si
148 Dinarina et al. grow "fields" of spindles on coverslips to investigate the relationship between chrom
149 ft lithography, and of silane-modified glass coverslips to reversibly seal the open side of the chann
150 hering to flat surfaces such as a microscope coverslip transmit cytoskeletally generated forces to th
151 ficiently on MAdCAM-1- than on VCAM-1-coated coverslips under conditions of flow.
152 r pH was monitored by imaging BCECF fixed to coverslips under dissociated cells.
153 erical ghosts were centrifuged onto a coated coverslip upon which they adhered.
154 ovalently attached to the surface of a glass coverslip using a fixed ratio of a native nucleotide and
155 es adjustment of bead height relative to the coverslip using a variant of optical force microscopy (t
156                                          The coverslip was mounted on a computer-controlled piezo-ele
157 ches of the LIS of MDCK cells grown on glass coverslips was indistinguishable from that in free solut
158 ng the attachment of the axonal shaft to the coverslip, we estimate values for the axial viscosity of
159 s to quantify proteins on the motility assay coverslip, we provide strong evidence that most of the M
160             By imaging samples on reflective coverslips, we enable simultaneous collection of four co
161                           Cells on companion coverslips were fixed with 3% p-formaldehyde and permeab
162 cropores in 130 mum thick borosilicate glass coverslips were functionalized with trichloro(1H,1H,2H,2
163                    Monolayers grown on glass coverslips were loaded with the pH-sensitive dye 2', 7'-
164           MK adhering to FN or FGN coated on coverslips were quantitated by a computerized image anal
165 reshly secreted plaques deposited onto glass coverslips were shown by matrix-assisted laser desorptio
166                               Cells grown on coverslips were similarly treated and probed with antibo
167                                          The coverslips were then moved to dishes containing either c
168                            Cells washed from coverslips were used to determined viable counts.
169   Our array-based technology enables "active coverslips" where, when scaled, many individually held c
170 ack-scattered light between the bead and the coverslip, whereas the noise inherent in a surface-tethe
171 e neurons are cultured on polylysine-treated coverslips, which are suspended above an astrocyte feede
172 and was chemisorbed to a standard microscope coverslip with (3-mercaptopropyl)trimethoxysilane.
173 single NP-UCNP in solution between slide and coverslip with diffusivity up to 10(-2) mum(2)s(-1).
174                    Cells were grown on glass coverslips with a microgrid pattern so that the results
175                                              Coverslips with cultured human coronary artery ECs were
176                        Resting MK adhered to coverslips with immobilized FN.
177 s were cultured overnight on collagen-coated coverslips with increasing concentrations of different b
178 rse cultures of hippocampal neurons grown on coverslips with no glia.
179 rulean-labeled protein proximal to the glass coverslip within individual granules.
180                 Cells were attached to glass coverslips within flow chambers that allowed application
181 g dilute solutions of Sylgard 184 onto glass coverslips, yielding approximately 1.4 microm thick film

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