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1 ellular assembly by immunohistochemistry and immunofluorescence microscopy.
2 s, were confirmed by electron microscopy and immunofluorescence microscopy.
3 Morphologic alterations are shown by using immunofluorescence microscopy.
4 MP co-receptor hemojuvelin was visualized by immunofluorescence microscopy.
5 ntent and capillarisation using quantitative immunofluorescence microscopy.
6 transcription-polymerase chain reaction and immunofluorescence microscopy.
7 rkers WT1 and synaptopodin, as determined by immunofluorescence microscopy.
8 lls, using deep transcriptome sequencing and immunofluorescence microscopy.
9 iopsies were studied by Western blotting and immunofluorescence microscopy.
10 O-GlcNAc and ZASP in Western blotting and by immunofluorescence microscopy.
11 visualizes translation in cells via standard immunofluorescence microscopy.
12 s were assessed by western blot and indirect immunofluorescence microscopy.
13 he influence of the labeling density in STED immunofluorescence microscopy.
14 n was evaluated by phospho-flow analysis and immunofluorescence microscopy.
15 muscle actin expression was assessed through immunofluorescence microscopy.
16 rotein epitopes on root cap cell walls using immunofluorescence microscopy.
17 ntent and capillarisation using quantitative immunofluorescence microscopy.
18 ined using PCR, immunoblotting, and confocal immunofluorescence microscopy.
19 T cells were assessed using immunofluorescence microscopy.
20 r exposure to CSF-1 for 2.5 min was shown by immunofluorescence microscopy.
21 and validated with the established method of immunofluorescence microscopy.
22 TNO1 was found to localize to the TGN by immunofluorescence microscopy.
23 ferent developmental stages using RT-PCR and immunofluorescence microscopy.
24 utant were confirmed by PCR, sequencing, and immunofluorescence microscopy.
25 (GLUT4) trafficking, as assessed by means of immunofluorescence microscopy.
26 protein, as determined by flow cytometry and immunofluorescence microscopy.
27 orescence-activated cell sorter analysis and immunofluorescence microscopy.
28 uman and mouse kidneys by immunoblotting and immunofluorescence microscopy.
29 on of this receptor was verified by confocal immunofluorescence microscopy.
30 8 localization as a helical array of foci by immunofluorescence microscopy.
31 ild type by immunoblot analysis and confocal immunofluorescence microscopy.
32 ions on muscle cell surface were examined by immunofluorescence microscopy.
33 ng cytosolic and mitochondrial fractions and immunofluorescence microscopy.
34 ntegrin, talin, and vinculin, as observed by immunofluorescence microscopy.
35 mistry; CD4 and FoxP3 were localized by dual immunofluorescence microscopy.
36 f differentiating 3T3-L1 preadipocytes using immunofluorescence microscopy.
37 k nuclear export of topo IIalpha as shown by immunofluorescence microscopy.
38 ocalization of sortase A using deconvolution immunofluorescence microscopy.
39 -transcription polymerase chain reaction and immunofluorescence microscopy.
40 electrophysiological analysis, and confocal immunofluorescence microscopy.
41 s of pheromone-induced cells as monitored by immunofluorescence microscopy.
42 nt increase in protein levels as detected by immunofluorescence microscopy.
43 Rp1h protein location was determined with immunofluorescence microscopy.
44 tegrin alpha(v) decorated the VWF strings by immunofluorescence microscopy.
45 Changes were monitored with phase and immunofluorescence microscopy.
46 ntent and capillarisation using quantitative immunofluorescence microscopy.
47 , as identified through Western blotting and immunofluorescence microscopy.
48 ivation, as determined by flow cytometry and immunofluorescence microscopy.
49 e protein levels were quantified by confocal immunofluorescence microscopy.
50 ing P. gingivalis infection was confirmed by immunofluorescence microscopy.
51 , which all localize to the AZs, as shown by immunofluorescence microscopy.
52 intracellular localization in HeLa cells by immunofluorescence microscopy.
53 t, adherent cell types that are required for immunofluorescence microscopy.
54 chemical markers, histological staining, and immunofluorescence microscopy.
55 APC were demonstrated through histology and immunofluorescence microscopy.
56 using multicolor flow cytometry and confocal immunofluorescence microscopy.
57 as assessed by flow cytometric assays and by immunofluorescence microscopy.
58 ified in isolated blood lymphocytes by using immunofluorescence microscopy after staining the phospho
60 ected by the loss of K7 and western blot and immunofluorescence microscopy analysis revealed that the
61 X to induce microtubule polymerization using immunofluorescence microscopy and a cell-based tubulin p
64 junction protein distribution with confocal immunofluorescence microscopy and antibodies against key
65 cDNA and determined their localization using immunofluorescence microscopy and biochemical assays.
67 ins on intact cells was analyzed by confocal immunofluorescence microscopy and by a novel cross linki
70 es in histone acetylation were determined by immunofluorescence microscopy and chromatin immunoprecip
73 ence of intraerythrocytic bacteria by double-immunofluorescence microscopy and ex vivo gentamicin pro
76 phase of hES and somatic cells using in situ immunofluorescence microscopy and fluorescence in situ h
78 ct the conformation of this polybasic motif, immunofluorescence microscopy and live cell imaging to i
81 platelets, as assessed biochemically, and by immunofluorescence microscopy and proximity ligation.
83 he subcellular localization of protein p6 by immunofluorescence microscopy and show that, at early in
84 tion factories were visualized with confocal immunofluorescence microscopy and single-replicon analys
87 s heterogeneously detected in mESC nuclei by immunofluorescence microscopy and this result correlated
90 ors (VPAC1 and 2) were determined by RT-PCR, immunofluorescence microscopy and Western blot analysis.
92 es and in cultures of human outflow cells by immunofluorescence microscopy and Western blot, respecti
96 , and fibronectin were evaluated by indirect immunofluorescence microscopy and/or Western blot analys
98 g bioluminescence resonance energy transfer, immunofluorescence microscopy, and co-immunoprecipitatio
99 Green fluorescent protein (GFP) fusions, immunofluorescence microscopy, and cryo-electron tomogra
100 a combination of immunoelectron microscopy, immunofluorescence microscopy, and functional analysis,
101 Ps) was investigated by immunoprecipitation, immunofluorescence microscopy, and HSP knockout using sm
102 hagosomes was confirmed by Western blotting, immunofluorescence microscopy, and immunoelectron micros
103 eruli at light microscopy, one glomerulus at immunofluorescence microscopy, and one glomerulus at ele
105 analysis was evaluated with flow cytometry, immunofluorescence microscopy, and short tandem repeat p
106 y determined by yeast cell agglutination and immunofluorescence microscopy, and the results were corr
107 g [Hh] pathway transcription factor Gli3) by immunofluorescence microscopy; and cilia function using
108 biochemical, subcellular fractionation, and immunofluorescence microscopy approaches to elucidate CP
109 ir ability to bind LPL were assessed with an immunofluorescence microscopy assay and a Western blot a
110 essed Akt membrane translocation as shown by immunofluorescence microscopy but left the concentration
111 d trafficking of Galphas and XLalphas, using immunofluorescence microscopy, cell fractionation, and t
112 ymerase chain reaction, immunoprecipitation, immunofluorescence microscopy, chromatin immunoprecipita
113 g bioluminescence resonance energy transfer, immunofluorescence microscopy, co-immunoprecipitation, a
120 lastoid cell lines, we previously showed how immunofluorescence microscopy could define the distribut
125 y in immature SOD1(G93A) spinal cords and by immunofluorescence microscopy detection of a longer pers
126 ut screens, we recently combined a classical immunofluorescence microscopy detection technique with f
128 nes for the report format, light microscopy, immunofluorescence microscopy, electron microscopy, and
132 by using quantitative PCR, ELISA, histology, immunofluorescence microscopy, flow cytometry, and metha
133 in the gentamicin protection assays, double-immunofluorescence microscopy, flow cytometry, scanning
134 (0, 2 and 6 h) were analysed using confocal immunofluorescence microscopy for fibre type-specific IM
135 with rheumatoid arthritis (RA) were examined immunofluorescence microscopy for the presence of lympho
138 essed by scanning electron microscopy (SEM), immunofluorescence microscopy, histochemistry and quanti
139 s followed by analyzing NSP4 localization by immunofluorescence microscopy identified the 61-83-amino
142 protein-fluorescent vancomycin 2D and 3D-SIM immunofluorescence microscopy (IFM) of cells at differen
143 tein 2D and 3D-SIM (structured illumination) immunofluorescence microscopy (IFM) showed that GpsB and
147 We constructed the system using confocal immunofluorescence microscopy images from the Human Prot
148 fied the presence of RPE65 in lamprey RPE by immunofluorescence microscopy, immunoblot and mass spect
149 Moreover, traditional analyses, including immunofluorescence microscopy, immunoblot, and microplat
150 and proteins were analyzed by using confocal immunofluorescence microscopy, immunoblotting, myelopero
151 ction was demonstrated on the graft sites by immunofluorescence microscopy in 9 of 10 biopsy samples
152 re absent or reduced on western blots and by immunofluorescence microscopy in cells containing null m
153 Using selective permeabilization indirect immunofluorescence microscopy in combination with glycos
156 combined Fura-2-based [Ca(2+)]i imaging with immunofluorescence microscopy in isolated split-opened d
158 17 SCID mice, the bacteria are detectable by immunofluorescence microscopy in neutrophils and macroph
159 nd its intracellular adaptor protein Dab2 by immunofluorescence microscopy in placental biopsies from
161 sucrose gradient centrifugation and indirect immunofluorescence microscopy indicated that most ROMK p
164 nuclear antigen (LANA) dots, as detected by immunofluorescence microscopy, indicating a higher viral
166 copy serration pattern analysis and indirect immunofluorescence microscopy knockout analysis are valu
169 in-CXCR3 interaction was further analyzed by immunofluorescence microscopy, laser capture microscopy,
170 d over wild-type), and quantitative confocal immunofluorescence microscopy localized over-expressed v
173 boratory has recently developed quantitative immunofluorescence microscopy methods to measure protein
174 studied by single DNA molecule analyses and immunofluorescence microscopy (molecular combing) showed
176 ride)-split human skin substrate by indirect immunofluorescence microscopy, not diagnosed epidermolys
177 eir validity via parabiosis and quantitative immunofluorescence microscopy of a mouse memory CD8 T ce
178 criteria are usually not sufficient, direct immunofluorescence microscopy of a perilesional biopsy s
184 so requires HA trimerization, as revealed by immunofluorescence microscopy of IAV-infected cells and
192 Subcellular localisation was observed by immunofluorescence microscopy of transfected HEK293 cell
196 ns was confirmed by immunohistochemistry and immunofluorescence microscopy on clinical samples and ti
199 romatin has traditionally been studied using immunofluorescence microscopy or biochemical cellular fr
200 e are many third-party data sources, such as immunofluorescence microscopy or protein annotations and
202 plating homogenates onto MacConkey agar, and immunofluorescence microscopy performed using anti-LPS a
203 rase chain reaction, immunoblot analysis, or immunofluorescence microscopy; proliferation was measure
205 olution stimulated emission depletion (STED) immunofluorescence microscopy resolved individual NPCs,
215 ppocampi from chronically stressed rats, and immunofluorescence microscopy revealed redistribution of
221 cell fractionation experiments and confocal immunofluorescence microscopy revealed that ET activates
223 nd identified by Western blots, and confocal immunofluorescence microscopy revealed that GPR17 and Cy
231 n gut, ovaries, and Malpighian tubules where immunofluorescence microscopy reveals that AgAQP1 reside
236 ealed increased numbers of glycosomes, while immunofluorescence microscopy showed increased and more
237 functions before DacB in D-Ala removal, and immunofluorescence microscopy showed that DacA and DacB
240 vo and analysis of frozen tissue sections by immunofluorescence microscopy showed that red cells from
241 both cytoplasmic and membrane fractions, and immunofluorescence microscopy showed that septin 7 is ex
245 Bsu)), which is localized at division septa, immunofluorescence microscopy showed that WalK(Spn) is d
246 ption profiling results were corroborated by immunofluorescence microscopy showing increased expressi
254 ke secreted (Pls) proteins and determined by immunofluorescence microscopy that Pls1 (CT049) and Pls2
255 on (based on gammaH2AX/53BP1 high-resolution immunofluorescence microscopy) that amifostine treatment
257 or flat mount preparations were subjected to immunofluorescence microscopy to detect blood vessels (i
258 We utilized quantitative PCR and double immunofluorescence microscopy to determine that both PPA
259 we fused Rob's CTD to SoxS and used indirect immunofluorescence microscopy to determine the effect of
260 Here, we employed bioinformatic analysis and immunofluorescence microscopy to examine the physiologic
262 re, we used a cell-based assay and automated immunofluorescence microscopy to screen 17,700 small mol
264 tion and inhibition tests were combined with immunofluorescence microscopy to show that the Wip1 gene
265 ne protein encoded by KCNE4, is localized by immunofluorescence microscopy to the transverse tubules
266 tions, or trypsin digestion and subjected to immunofluorescence microscopy to visualize vessels using
268 bule network was visualized in HeLa cells by immunofluorescence microscopy using Bimolecular Fluoresc
269 examined by immunohistology and quantitative immunofluorescence microscopy using lymphatic endothelia
278 blotting, immunohistochemistry, and confocal immunofluorescence microscopy, we analyzed the cell surf
282 Using fluorescent in situ hybridization and immunofluorescence microscopy, we found that Ty1 mRNA an
286 SSP3-specific antibodies in conjunction with immunofluorescence microscopy, we showed that SSP3 is ex
287 g confocal and stimulated emission depletion immunofluorescence microscopy, we showed that VHC-I had
288 scopy, transmission electron microscopy, and immunofluorescence microscopy were performed to ascertai
289 lymerase chain reaction, immunoblotting, and immunofluorescence microscopy were used for expression s
291 inylation, immobilized lectins, and confocal immunofluorescence microscopy were used to characterize
293 -associated BIG1 and BIG2, which by confocal immunofluorescence microscopy were widely dispersed from
295 ic and membrane antigens using deconvolution immunofluorescence microscopy will facilitate further st
297 luorescent protein (eGFP) fusion protein and immunofluorescence microscopy with anti-BetA antibodies,
299 ence assays with recombinant bacteria and by immunofluorescence microscopy with purified proteins.
300 tegrating transcriptomics and antibody-based immunofluorescence microscopy with validation by mass sp
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