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1 present in SEC based on Western blotting and confocal immunofluorescence microscopy.
2 as detected by membrane subfractionation and confocal immunofluorescence microscopy.
3 pathway, as determined by epifluorescent and confocal immunofluorescence microscopy.
4 lut4 in muscle sections as observed by laser confocal immunofluorescence microscopy.
5 by canine kidney cell lines was studied with confocal immunofluorescence microscopy.
6 were examined using PCR, immunoblotting, and confocal immunofluorescence microscopy.
7 expression of this receptor was verified by confocal immunofluorescence microscopy.
8 ed with wild type by immunoblot analysis and confocal immunofluorescence microscopy.
9 criteria, electrophysiological analysis, and confocal immunofluorescence microscopy.
10 5 relative protein levels were quantified by confocal immunofluorescence microscopy.
11 lin and B23 at a frequency of nearly 100% by confocal immunofluorescence microscopy.
12 with human macrophages by immunoelectron and confocal immunofluorescence microscopy.
13 roteins was determined using immunoblots and confocal immunofluorescence microscopy.
14 IGFBP-3 surface coating was identified by confocal immunofluorescence microscopy.
15 lyzed by using multicolor flow cytometry and confocal immunofluorescence microscopy.
16 mbranes (CNVMs) was analyzed by double-label confocal immunofluorescence microscopy.
17 nd a change in cell shape as demonstrated by confocal immunofluorescence microscopy.
18 mitochondria, as revealed by double-labeling confocal immunofluorescence microscopy.
19 ese methods and conclusions were obtained by confocal immunofluorescence microscopy.
20 ance during the period of study as imaged by confocal immunofluorescence microscopy.
21 tein primarily localized near termini) under confocal immunofluorescence microscopy.
22 lear staining in all cell lines tested using confocal immunofluorescence microscopy.
23 n the surface of mast cells as determined by confocal immunofluorescence microscopy, aberrant S1P rec
24 GT) has been studied in human fibroblasts by confocal immunofluorescence microscopy after intranuclea
25 rcellular junction protein distribution with confocal immunofluorescence microscopy and antibodies ag
27 cdk6 to the nucleus, as demonstrated by both confocal immunofluorescence microscopy and biochemical f
28 two proteins on intact cells was analyzed by confocal immunofluorescence microscopy and by a novel cr
30 atory responses of TNF, has been analyzed by confocal immunofluorescence microscopy and by Western bl
31 e cellular distribution of phospho-ERK1/2 by confocal immunofluorescence microscopy and cellular frac
33 ecame spatially colocalized as determined by confocal immunofluorescence microscopy and fluorescence
34 eta-hydroxylase (DbetaH) was performed using confocal immunofluorescence microscopy and immunoelectro
36 r replication factories were visualized with confocal immunofluorescence microscopy and single-replic
40 was demonstrated within cultured neurons by confocal immunofluorescence microscopy and within neuron
42 inases by co-immunoprecipitation studies and confocal immunofluorescence microscopy, and this interac
43 s (ANP-RB, a guanylyl cyclase), we have used confocal immunofluorescence microscopy applied to primar
46 yonic to adult mice by immunohistochemistry, confocal immunofluorescence microscopy, catalyzed report
50 0-kd band in control and TC-grown cells, and confocal immunofluorescence microscopy demonstrated stai
54 biopsies (0, 2 and 6 h) were analysed using confocal immunofluorescence microscopy for fibre type-sp
56 ormation and proteins were analyzed by using confocal immunofluorescence microscopy, immunoblotting,
57 artially colocalized with Rab38 and Rab32 by confocal immunofluorescence microscopy in MNT-1 cells.
61 g retina, RPE, and choroid was processed for confocal immunofluorescence microscopy, laser capture mi
62 (5.4 fold over wild-type), and quantitative confocal immunofluorescence microscopy localized over-ex
67 lected deleted Env proteins was confirmed by confocal immunofluorescence microscopy of hemagglutinin-
77 ation of CaMK and GABA immunoreactivity with confocal immunofluorescence microscopy revealed that CaM
78 rikingly, cell fractionation experiments and confocal immunofluorescence microscopy revealed that ET
79 pitated and identified by Western blots, and confocal immunofluorescence microscopy revealed that GPR
86 he intracellular neutralization experiments, confocal immunofluorescence microscopy showed prominent
89 reased FYB tyrosine phosphorylation, whereas confocal immunofluorescence microscopy showed that FYB c
94 rol or nocodazole-treated cells was found by confocal immunofluorescence microscopy to be a single ch
96 fully the assembly of the MTOC-TMA, we used confocal immunofluorescence microscopy to examine the lo
97 ved from B-cell-deficient mice were found by confocal immunofluorescence microscopy to express outer
98 ation and immunoblot assay, and were used in confocal immunofluorescence microscopy to reveal low lev
101 ion were monitored in GH-stimulated cells by confocal immunofluorescence microscopy using an antibody
102 olgi network (TGN) morphology as revealed by confocal immunofluorescence microscopy using antibody to
103 of Cx43 were measured by immunoblotting and confocal immunofluorescence microscopy using isoform-spe
109 Western blotting, immunohistochemistry, and confocal immunofluorescence microscopy, we analyzed the
110 mistry, HIV-1 RNA in situ hybridization, and confocal immunofluorescence microscopy, we demonstrate t
112 nventional and immunoelectron microscopy and confocal immunofluorescence microscopy, we show that Gol
114 face biotinylation, immobilized lectins, and confocal immunofluorescence microscopy were used to char
115 his study, a murine macrophage cell line and confocal immunofluorescence microscopy were used to more
116 membrane-associated BIG1 and BIG2, which by confocal immunofluorescence microscopy were widely dispe
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