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1 d of osteoprotegerin (OPG) were evaluated by immunofluorescent staining.
2 e contrast agent (Eu-P947) with specific MMP immunofluorescent staining.
3 ong the z axis, as well as depth-independent immunofluorescent staining.
4 ity of CR-1 by fluorescent cell-labeling and immunofluorescent staining.
5 ectin (FN) was monitored by Western blot and immunofluorescent staining.
6 tic fibers in ONH tissue was investigated by immunofluorescent staining.
7 adhesion molecule (LECAM)-1 were detected by immunofluorescent staining.
8 hole-cell patch-clamp analysis, confirmed by immunofluorescent staining.
9 nsity were determined by immunohistochemical immunofluorescent staining.
10 d HLA class II (IA) antigen were assessed by immunofluorescent staining.
11 21(Cip1), and p27(Kip1) was determined using immunofluorescent staining.
12 subjects and SS ATD-affected patients using immunofluorescent staining.
13 d slow MHC after 12 d in culture, as seen by immunofluorescent staining.
14 by subcellular fractionation experiments and immunofluorescent staining.
15 RSBP-1 to trypsin digestion, and by indirect immunofluorescent staining.
16 p47 and type I procollagen was determined by immunofluorescent staining.
17 uated aggregates of tubulin were found by an immunofluorescent staining.
18 The number of LCs was enumerated by immunofluorescent staining.
19 d by ELISA, zymography, Western blotting and immunofluorescent staining.
20 bly transfected with the prothrombin cDNA by immunofluorescent staining.
21 tools followed by acid-fast staining (AF) or immunofluorescent staining.
22 s of cytoplasmic microtubules as revealed by immunofluorescent staining.
23 rences were supported by lineage tracing and immunofluorescent staining.
24 e the expression of senescence biomarkers by immunofluorescent staining.
25 stained for CB1 and uncoupling protein-1 by immunofluorescent staining.
26 eration in mutant epithelium, as revealed by immunofluorescent staining.
27 IL-15, as indicated by Western blotting and immunofluorescent staining.
28 ugated dextran, and (ii) AJC structure using immunofluorescent staining.
29 valuated using qRT-PCR, western blotting and immunofluorescent staining.
30 by quantitative PCR (qPCR), immunoblots, and immunofluorescent staining.
31 rn blot and of protein expression by IHC and immunofluorescent staining.
32 e, HBx-mSin3A colocalization was detected by immunofluorescent staining.
33 transplantation model by flow cytometry and immunofluorescent staining.
34 lular localization of FKBP10 was assessed by immunofluorescent stainings.
35 dispersed rat islet cells analyzed by double immunofluorescent staining, 90% of the insulin, 76% of t
36 nterferon-gamma (IFNgamma) were confirmed by immunofluorescent staining and affinity precipitation as
37 termined with protein gene product (PGP) 9.5 immunofluorescent staining and blinded and automated ima
38 ISC1, PCM1, and BBS proteins was assessed by immunofluorescent staining and coimmunoprecipitation.
39 iatric control subjects were used for double immunofluorescent staining and confocal image analysis.
40 PML/Nur77 colocalized in vivo in a double immunofluorescent staining and confocal microscopic anal
41 y epithelium of guinea pigs were examined by immunofluorescent staining and confocal microscopy in wh
46 identified by the fluorescence "halo" after immunofluorescent staining and could be retrieved by sit
47 r localization of proteins was determined by immunofluorescent staining and expression of cyclin-depe
50 CR-5 on their cell membranes, as analyzed by immunofluorescent staining and flow cytometric analyses.
52 yzed these cells utilizing quantitative-PCR, immunofluorescent staining and flow cytometry analysis.
53 ce of these observations was demonstrated by immunofluorescent staining and flow cytometry of lymphoc
64 n B-CLL clones and approaches involving both immunofluorescent staining and pharmacologic inhibitors,
66 was studied in knockout mice by using double immunofluorescent staining and real-time polymerase chai
67 MMP14 (MT1-MMP)-haploinsufficient mice using immunofluorescent staining and scanning electron microsc
68 ed with activated microglia were examined by immunofluorescent staining and semiquantitative real-tim
69 levels were evaluated in human PAH lungs by immunofluorescent staining and single cell RNA sequencin
70 r the presence of EETs and S aureus by using immunofluorescent staining and the PNA-Fish assay, respe
71 ssive, confluent clusters as demonstrated by immunofluorescent staining and TissueFAXS quantitative i
73 HCE cells and corneal epithelium of rats by immunofluorescent staining and Western blot analysis.
74 ings were corroborated by electrophysiology, immunofluorescent staining, and biotinylation of surface
75 cycle-regulatory proteins was determined by immunofluorescent staining, and expression of the protei
78 n be applied to immunoblotting, cell surface immunofluorescent staining, and immunohistochemistry at
79 e real-time polymerase chain reaction (PCR), immunofluorescent staining, and in situ hybridization we
82 nt of jagged-1 in tip cells was confirmed by immunofluorescent staining as well as by laser capture m
83 series of postmortem immunohistochemical and immunofluorescent stainings, as well as Western blot ana
84 By using Northern blot, Western blot, and immunofluorescent staining assays, we showed that Nur77
86 ts such as ciliary ultrastructural analysis, immunofluorescent staining, ciliary beat assessment, and
91 experiments, proximity ligation assays, and immunofluorescent staining confirmed the interaction bet
94 safety of this treatment were examined using immunofluorescent staining, confocal imaging, immunoelec
105 neighboring inducing cells, as determined by immunofluorescent staining, demonstrating that de novo v
109 in, Tmod, and tropomyosin were determined by immunofluorescent staining followed by confocal microsco
110 ed expression of PAM-1 also caused decreased immunofluorescent staining for ACTH, a product of proopi
112 With affinity-purified reagents, we observed immunofluorescent staining for both AML1 and ETO in the
113 Infiltrates were confirmed histologically by immunofluorescent staining for CD3+ and CD11b+ cells.
114 ht microscopy, including immunohistochemical/immunofluorescent staining for CD31, CD105, and HMB45, a
116 confocal laser microscopic analyses of dual immunofluorescent staining for CYP1A1/1A2 and cytokerati
119 this finding explains the unusual pattern of immunofluorescent staining for F.IX shown in these exper
124 oupled recombinant gelonin (rGel), there was immunofluorescent staining for rGel within choroidal neo
125 and myofibroblasts, as determined by double-immunofluorescent staining for TF and cell type-specific
127 ivity was assessed in ATC patient tissues by immunofluorescent staining for the autophagy marker micr
130 ated by confocal microscopy of three-channel immunofluorescent staining for the proliferation marker
135 e location, intensity, and rate of change of immunofluorescent staining, Hailey-Hailey and normal ker
138 processes that were prominent in subsequent immunofluorescent staining images but not with classical
140 us and distinct from ND-10 as defined by PML immunofluorescent staining in CIN lesions, condylomata,
141 lization of IAIPs and HMGB1 were detected by immunofluorescent staining in control and rats immediate
142 T and B cells in the blood was determined by immunofluorescent staining in hosts bearing long-term (>
143 y Western blot and flow cytometry as well as immunofluorescent staining in primary sinus epithelial c
146 polymerase chain reaction in total liver and immunofluorescent staining in tissues for synaptophysin
151 ns could be simultaneously isolated and, via immunofluorescent staining, individually identified and
153 ent of the transporter protein occurs; (iii) immunofluorescent staining of 24-h fed and starved cells
157 Endothelial cell culture and preliminary immunofluorescent staining of Anaplasma-infected tissues
166 fractions of chicken embryo heart cells and immunofluorescent staining of chicken embryo cardiocytes
170 cell and TM cell markers were identified by immunofluorescent staining of cryosections or tissue who
172 a possible defect in the centromeric region, immunofluorescent staining of cyclin A1 protein shows lo
173 smission electron microscopy of sections and immunofluorescent staining of cytoskeletal proteins in w
174 he affinity-purified antibodies were used in immunofluorescent staining of developing limbs and matri
176 rmed on tissue sections with the use of dual immunofluorescent staining of endothelium and the fluore
177 re authenticated by CD31 immunoblotting, and immunofluorescent staining of established EC markers VE-
182 mission electron microscopy of glomeruli and immunofluorescent staining of glomerular epithelial cell
184 located in mitochondria as evidenced by the immunofluorescent staining of HepG2 cells with specific
188 nd characteristic birefringent "needles." By immunofluorescent staining of known myofibril components
190 by replacing ClO(-) with SP in vivo, and by immunofluorescent staining of large airways of exposed m
194 presence of RuV in skin specimens using RuV immunofluorescent staining of paraffin-embedded tissue s
213 oma, we performed in situ hybridizations and immunofluorescent stainings on human immunodeficiency vi
214 aracterized by hyperphosphorylated tau (AT8; immunofluorescent staining) pathological inclusions, neu
216 cofractionates with yeast NPCs and gives an immunofluorescent staining pattern typical of nucleopori
217 Both antisera gave the same distinctive immunofluorescent staining pattern, with unstained heter
221 This was addressed by immunohistochemical/immunofluorescent stainings performed on grafted tissue
223 ated single chromatids, their morphology and immunofluorescent staining properties were strikingly si
225 g qRT-PCR, immunoprecipitation/Western blot, immunofluorescent staining, radio-thin-layer chromatogra
228 tabase including the addition of subcellular immunofluorescent staining results from the Human Protei
242 In the bone marrow transplant mice, double immunofluorescent staining revealed that the combination
244 alian cells with mNAT1 and mARD1 followed by immunofluorescent staining revealed that these proteins
249 ampal degeneration in C57BL/6 mice, in which immunofluorescent staining showed a 28% loss of PSD95-po
257 l populations in lung tissue cryosections by immunofluorescent staining showed sparse bacteria within
269 ental profiles using electron microscopy and immunofluorescent staining suggest that cell fusions are
271 protein in cells by immunohistochemical and immunofluorescent staining techniques and examined coloc
272 olocalization of endogenous Irgm1, using two immunofluorescent staining techniques, either in fibrobl
275 B and the annexin II tetramer were shown by immunofluorescent staining to colocalize on the surface
277 methods may require the presence of 50,000 (immunofluorescent staining) to 500,000 (AF) oocysts per
280 terograde tracing combined with triple label immunofluorescent staining was conducted to examine the
287 nfocal microscopy (LSCM) in combination with immunofluorescent staining, we simultaneously measured i
288 hanges in MMP protein expression detected by immunofluorescent staining were similar to changes in ge
295 enzyme-linked immunosorbent assay (ELISA) or immunofluorescent staining with confocal laser scanning
297 reen fluorescent protein-tagged proteins and immunofluorescent staining with specific anti-peptide an
299 e sympathetic ganglion neurons by RT-PCR and immunofluorescent staining, with expression occurring be
300 sectioning followed by standard histology or immunofluorescent staining without loss of fluorescence