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1 ong the z axis, as well as depth-independent immunofluorescent staining.
2 ity of CR-1 by fluorescent cell-labeling and immunofluorescent staining.
3 ectin (FN) was monitored by Western blot and immunofluorescent staining.
4 tic fibers in ONH tissue was investigated by immunofluorescent staining.
5 adhesion molecule (LECAM)-1 were detected by immunofluorescent staining.
6 hole-cell patch-clamp analysis, confirmed by immunofluorescent staining.
7 d by ELISA, zymography, Western blotting and immunofluorescent staining.
8 nsity were determined by immunohistochemical immunofluorescent staining.
9 d HLA class II (IA) antigen were assessed by immunofluorescent staining.
10 21(Cip1), and p27(Kip1) was determined using immunofluorescent staining.
11  subjects and SS ATD-affected patients using immunofluorescent staining.
12 d slow MHC after 12 d in culture, as seen by immunofluorescent staining.
13 by subcellular fractionation experiments and immunofluorescent staining.
14 RSBP-1 to trypsin digestion, and by indirect immunofluorescent staining.
15 p47 and type I procollagen was determined by immunofluorescent staining.
16  stained for CB1 and uncoupling protein-1 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 bly transfected with the prothrombin cDNA by immunofluorescent staining.
20 tools followed by acid-fast staining (AF) or immunofluorescent staining.
21 s of cytoplasmic microtubules as revealed by immunofluorescent staining.
22 ugated dextran, and (ii) AJC structure using immunofluorescent staining.
23 by quantitative PCR (qPCR), immunoblots, and immunofluorescent staining.
24 rn blot and of protein expression by IHC and immunofluorescent staining.
25 e, HBx-mSin3A colocalization was detected by immunofluorescent staining.
26  transplantation model by flow cytometry and immunofluorescent staining.
27 e contrast agent (Eu-P947) with specific MMP immunofluorescent staining.
28 lular localization of FKBP10 was assessed by immunofluorescent stainings.
29 dispersed rat islet cells analyzed by double immunofluorescent staining, 90% of the insulin, 76% of t
30 nterferon-gamma (IFNgamma) were confirmed by immunofluorescent staining and affinity precipitation as
31 ISC1, PCM1, and BBS proteins was assessed by immunofluorescent staining and coimmunoprecipitation.
32 iatric control subjects were used for double immunofluorescent staining and confocal image analysis.
33    PML/Nur77 colocalized in vivo in a double immunofluorescent staining and confocal microscopic anal
34 y epithelium of guinea pigs were examined by immunofluorescent staining and confocal microscopy in wh
35                                 We have used immunofluorescent staining and confocal microscopy to ex
36 s it in rat NTS by using multiple labels for immunofluorescent staining and confocal microscopy.
37 nd guinea pig OHCs was re-examined by use of immunofluorescent staining and confocal microscopy.
38  identified by the fluorescence "halo" after immunofluorescent staining and could be retrieved by sit
39 r localization of proteins was determined by immunofluorescent staining and expression of cyclin-depe
40 CR-5 on their cell membranes, as analyzed by immunofluorescent staining and flow cytometric analyses.
41                                              Immunofluorescent staining and flow cytometric analysis
42 yzed these cells utilizing quantitative-PCR, immunofluorescent staining and flow cytometry analysis.
43 ce of these observations was demonstrated by immunofluorescent staining and flow cytometry of lymphoc
44                                  Competitive immunofluorescent staining and flow cytometry reveal tha
45 was also examined in a subset of patients by immunofluorescent staining and flow cytometry.
46 rculating human EPCs were characterized with immunofluorescent staining and flow cytometry.
47                         In the present work, immunofluorescent staining and green fluorescent protein
48                                 We also used immunofluorescent staining and histology coupled with el
49                                              Immunofluorescent staining and immunoprecipitation exper
50 tive for (18)F-FMPEP-d2, consistent with the immunofluorescent staining and in vitro results.
51                                              Immunofluorescent staining and laser scanning confocal m
52                                        Using immunofluorescent staining and live cell imaging of fluo
53                                              Immunofluorescent staining and microarray analyses sugge
54                                              Immunofluorescent staining and quantitative image analys
55 was studied in knockout mice by using double immunofluorescent staining and real-time polymerase chai
56 MMP14 (MT1-MMP)-haploinsufficient mice using immunofluorescent staining and scanning electron microsc
57 ed with activated microglia were examined by immunofluorescent staining and semiquantitative real-tim
58 r the presence of EETs and S aureus by using immunofluorescent staining and the PNA-Fish assay, respe
59 ssive, confluent clusters as demonstrated by immunofluorescent staining and TissueFAXS quantitative i
60                                         Both immunofluorescent staining and western blot analysis cor
61  HCE cells and corneal epithelium of rats by immunofluorescent staining and Western blot analysis.
62 ings were corroborated by electrophysiology, immunofluorescent staining, and biotinylation of surface
63  cycle-regulatory proteins was determined by immunofluorescent staining, and expression of the protei
64 ed by using RT-PCR, ELISA, Western blotting, immunofluorescent staining, and flow cytometry.
65 ive polymerase chain reaction, dual-labeling immunofluorescent staining, and immunoassays.
66 n be applied to immunoblotting, cell surface immunofluorescent staining, and immunohistochemistry at
67 e real-time polymerase chain reaction (PCR), immunofluorescent staining, and in situ hybridization we
68                         Immunoprecipitation, immunofluorescent staining, and RT-PCR of human VSMCs sh
69 f RIP1 was monitored by reporter gene assay, immunofluorescent staining, and Western blotting.
70 nt of jagged-1 in tip cells was confirmed by immunofluorescent staining as well as by laser capture m
71 series of postmortem immunohistochemical and immunofluorescent stainings, as well as Western blot ana
72    By using Northern blot, Western blot, and immunofluorescent staining assays, we showed that Nur77
73                                  VE-cadherin immunofluorescent staining at endothelial AJs and AJ wid
74 ts such as ciliary ultrastructural analysis, immunofluorescent staining, ciliary beat assessment, and
75                                              Immunofluorescent staining confirmed expression of the f
76                                              Immunofluorescent staining confirmed that SFRP2 and FMO1
77                                              Immunofluorescent staining confirmed that TNF-alpha was
78                                              Immunofluorescent staining confirmed the presence of the
79                                              Immunofluorescent staining confirmed this region-specifi
80 safety of this treatment were examined using immunofluorescent staining, confocal imaging, immunoelec
81                              Flow cytometry, immunofluorescent staining, confocal microscopy, and ana
82                                              Immunofluorescent staining demonstrated a ring-like fluo
83                                              Immunofluorescent staining demonstrated junctional gap f
84                                              Immunofluorescent staining demonstrated microglia activa
85                                              Immunofluorescent staining demonstrated that administrat
86                                       Double immunofluorescent staining demonstrated that Ca(v) 3.3-l
87                      Both immunoblotting and immunofluorescent staining demonstrated that PKCepsilon,
88                Gene expression profiling and immunofluorescent staining demonstrated that the express
89                                              Immunofluorescent stainings demonstrated localization to
90                                              Immunofluorescent staining demonstrates failure of nucle
91 neighboring inducing cells, as determined by immunofluorescent staining, demonstrating that de novo v
92                                              Immunofluorescent staining detects overlapping expressio
93                                              Immunofluorescent staining determined that the distance
94                                 By combining immunofluorescent staining, fluorescence in situ hybridi
95 in, Tmod, and tropomyosin were determined by immunofluorescent staining followed by confocal microsco
96 ed expression of PAM-1 also caused decreased immunofluorescent staining for ACTH, a product of proopi
97                               The pattern of immunofluorescent staining for alpha-SMA and TNC at the
98 With affinity-purified reagents, we observed immunofluorescent staining for both AML1 and ETO in the
99 Infiltrates were confirmed histologically by immunofluorescent staining for CD3+ and CD11b+ cells.
100 ht microscopy, including immunohistochemical/immunofluorescent staining for CD31, CD105, and HMB45, a
101           Combined in situ hybridization and immunofluorescent staining for CUGBP1 and CUGBP2, the 2
102  confocal laser microscopic analyses of dual immunofluorescent staining for CYP1A1/1A2 and cytokerati
103                         Immunoperoxidase and immunofluorescent staining for CYP1A1/1A2 was detected w
104                                      Minimal immunofluorescent staining for D1B DA receptor proteins
105 this finding explains the unusual pattern of immunofluorescent staining for F.IX shown in these exper
106                                              Immunofluorescent staining for hexokinase I showed no di
107                                     Positive immunofluorescent staining for IL-1 alpha, mature IL-1 b
108                   This was done by combining immunofluorescent staining for MOR1 or DOR1 with that fo
109      The number of pericytes was measured by immunofluorescent staining for NG2 proteoglycan.
110 oupled recombinant gelonin (rGel), there was immunofluorescent staining for rGel within choroidal neo
111  and myofibroblasts, as determined by double-immunofluorescent staining for TF and cell type-specific
112                                       Double-immunofluorescent staining for TF and transforming growt
113 ivity was assessed in ATC patient tissues by immunofluorescent staining for the autophagy marker micr
114                                              Immunofluorescent staining for the corresponding vascula
115                                    Moreover, immunofluorescent staining for the lysosomal protease ca
116 ated by confocal microscopy of three-channel immunofluorescent staining for the proliferation marker
117                        We therefore combined immunofluorescent staining for VR1 and NK1 to show that
118                Western blotting analysis and immunofluorescent staining further showed that only calc
119                      Sequential bindings and immunofluorescent staining further suggest that 1) TM5 b
120 e location, intensity, and rate of change of immunofluorescent staining, Hailey-Hailey and normal ker
121                                  By indirect immunofluorescent staining, hGH was detected on the surf
122                                              Immunofluorescent staining identified focal concentratio
123  processes that were prominent in subsequent immunofluorescent staining images but not with classical
124                                              Immunofluorescent staining, immunoblot, and Western blot
125 us and distinct from ND-10 as defined by PML immunofluorescent staining in CIN lesions, condylomata,
126 T and B cells in the blood was determined by immunofluorescent staining in hosts bearing long-term (>
127 y Western blot and flow cytometry as well as immunofluorescent staining in primary sinus epithelial c
128                           Using double-label immunofluorescent staining in situ, we showed that infil
129           In this study, Xin was analyzed by immunofluorescent staining in skeletal muscle samples fr
130 polymerase chain reaction in total liver and immunofluorescent staining in tissues for synaptophysin
131                                              Immunofluorescent staining indicated that C6ORF32 locali
132                                     However, immunofluorescent staining indicated that FIP200 was pre
133                                              Immunofluorescent staining indicated that insulin pretre
134                                       Double-immunofluorescent staining indicated that the majority o
135 ns could be simultaneously isolated and, via immunofluorescent staining, individually identified and
136                                              Immunofluorescent staining is an informative tool that i
137 ent of the transporter protein occurs; (iii) immunofluorescent staining of 24-h fed and starved cells
138                                              Immunofluorescent staining of A549 cells showed a fibril
139                                              Immunofluorescent staining of adherens junctions confirm
140                                              Immunofluorescent staining of alpha-actin revealed that
141     Endothelial cell culture and preliminary immunofluorescent staining of Anaplasma-infected tissues
142        Furthermore, confocal microscopy with immunofluorescent staining of articular chondrocytes con
143                                              Immunofluorescent staining of bacterium-infected calvari
144                                              Immunofluorescent staining of BCCV-infected cells reveal
145                                              Immunofluorescent staining of both whole bladder tissue
146                                              Immunofluorescent staining of BRCA1 and gamma-H2AX indic
147                                              Immunofluorescent staining of C/EBPbeta revealed that A-
148                          TER measurement and immunofluorescent staining of cadherins after a calcium
149                                              Immunofluorescent staining of cells with PINCH-2-specifi
150  fractions of chicken embryo heart cells and immunofluorescent staining of chicken embryo cardiocytes
151                                              Immunofluorescent staining of chicken osteoclasts confir
152                                              Immunofluorescent staining of collagen IV and laminin an
153                                              Immunofluorescent staining of corneal tissue in vivo dem
154  cell and TM cell markers were identified by immunofluorescent staining of cryosections or tissue who
155                                              Immunofluorescent staining of cultured hippocampal neuro
156 a possible defect in the centromeric region, immunofluorescent staining of cyclin A1 protein shows lo
157 smission electron microscopy of sections and immunofluorescent staining of cytoskeletal proteins in w
158 he affinity-purified antibodies were used in immunofluorescent staining of developing limbs and matri
159 rmed on tissue sections with the use of dual immunofluorescent staining of endothelium and the fluore
160              Consistent with these findings, immunofluorescent staining of fast but not slow muscle m
161                                       Triple immunofluorescent staining of fetal and adult pancreases
162                                              Immunofluorescent staining of G-kinase was predominantly
163        However, in the Ts65Dn mouse a strong immunofluorescent staining of GIRK2 was detected in the
164 mission electron microscopy of glomeruli and immunofluorescent staining of glomerular epithelial cell
165                                              Immunofluorescent staining of HeLa and L929 cells using
166  located in mitochondria as evidenced by the immunofluorescent staining of HepG2 cells with specific
167                                              Immunofluorescent staining of HUVEC colocalized ICE expr
168                                              Immunofluorescent staining of in vitro-cultivated or hos
169                                              Immunofluorescent staining of islet isografts infected w
170 nd characteristic birefringent "needles." By immunofluorescent staining of known myofibril components
171                                    Live cell immunofluorescent staining of L1 demonstrated that most
172  by replacing ClO(-) with SP in vivo, and by immunofluorescent staining of large airways of exposed m
173                                              Immunofluorescent staining of lumbar DRG demonstrated th
174                                              Immunofluorescent staining of markers for activated endo
175        Biochemical fractionation studies and immunofluorescent staining of murine brain slices reveal
176                                Histology and immunofluorescent staining of PKC and epidermal growth f
177                                     Indirect immunofluorescent staining of purified P. carinii organi
178                                              Immunofluorescent staining of rat sciatic nerve showed t
179                                     Indirect immunofluorescent staining of SCC cryosections and Weste
180                                              Immunofluorescent staining of T84 cells demonstrated the
181                                              Immunofluorescent staining of TCR-transduced cells with
182                                              Immunofluorescent staining of the cells with beta-tubuli
183 ocal microscopy provided cross validation by immunofluorescent staining of the compartments.
184                                              Immunofluorescent staining of the junctional proteins VE
185                                              Immunofluorescent staining of the microtubule network re
186                                              Immunofluorescent staining of the T-cell line with the p
187                                              Immunofluorescent staining of the tissue sections reveal
188                                              Immunofluorescent staining of the WT1 protein in 3T3 and
189                                              Immunofluorescent staining of thin sections of b/b and +
190                                              Immunofluorescent staining of tumour sections from human
191                                     Notably, immunofluorescent staining of viral proteins revealed an
192                                              Immunofluorescent staining on testis sections with the m
193 oma, we performed in situ hybridizations and immunofluorescent stainings on human immunodeficiency vi
194 aracterized by hyperphosphorylated tau (AT8; immunofluorescent staining) pathological inclusions, neu
195                                 Although the immunofluorescent staining pattern of several Golgi prot
196  cofractionates with yeast NPCs and gives an immunofluorescent staining pattern typical of nucleopori
197      Both antisera gave the same distinctive immunofluorescent staining pattern, with unstained heter
198                                          The immunofluorescent staining patterns produced by each ant
199                                              Immunofluorescent staining patterns were also consistent
200                     Mitogenic activation and immunofluorescent staining performed inside the microflu
201    This was addressed by immunohistochemical/immunofluorescent stainings performed on grafted tissue
202                                              Immunofluorescent staining produced by incubation with t
203 ated single chromatids, their morphology and immunofluorescent staining properties were strikingly si
204 elated well with the quantified results from immunofluorescent staining (r = 0.98).
205 g qRT-PCR, immunoprecipitation/Western blot, immunofluorescent staining, radio-thin-layer chromatogra
206                                 When used in immunofluorescent staining reactions using GVL peptide-l
207 oscopy and in intestinal epithelial cells by immunofluorescent staining, respectively.
208 tabase including the addition of subcellular immunofluorescent staining results from the Human Protei
209 of MALDI-IMS data with subsequently acquired immunofluorescent staining results.
210                                       Double immunofluorescent staining revealed a co-expression of W
211                                Surprisingly, immunofluorescent staining revealed a cytoplasmic misloc
212                                              Immunofluorescent staining revealed a dynamic ECM remode
213                                     However, immunofluorescent staining revealed an increased frequen
214                                              Immunofluorescent staining revealed constitutive and ind
215                                              Immunofluorescent staining revealed impairment of photor
216                                              Immunofluorescent staining revealed localization of the
217                                              Immunofluorescent staining revealed low levels of cortac
218                    Western blot analysis and immunofluorescent staining revealed mitochondrial p53 tr
219                                              Immunofluorescent staining revealed reduced surface expr
220                                              Immunofluorescent staining revealed that CGRP-Rs are abu
221                                              Immunofluorescent staining revealed that in the LA, type
222   In the bone marrow transplant mice, double immunofluorescent staining revealed that the combination
223                                              Immunofluorescent staining revealed that the cTaxREB107
224 alian cells with mNAT1 and mARD1 followed by immunofluorescent staining revealed that these proteins
225                                              Immunofluorescent staining revealed the presence of STAT
226               Additional localization, using immunofluorescent staining, revealed clustering in apica
227                                              Immunofluorescent staining reveals striking juxtanuclear
228                      Immunohistochemical and immunofluorescent staining show that ODN treatment drama
229 ampal degeneration in C57BL/6 mice, in which immunofluorescent staining showed a 28% loss of PSD95-po
230                                              Immunofluorescent staining showed a significant reductio
231                                       Double immunofluorescent staining showed aberrant co-localizati
232                          In addition, double immunofluorescent staining showed co-localization of end
233                                              Immunofluorescent staining showed higher numbers of CD31
234                                              Immunofluorescent staining showed nuclear localization i
235                                              Immunofluorescent staining showed redistribution of alph
236 l populations in lung tissue cryosections by immunofluorescent staining showed sparse bacteria within
237                                  Analysis by immunofluorescent staining showed that MAGP-2 overexpres
238                                              Immunofluorescent staining showed that Panx1 expression
239            Laser capture microdissection and immunofluorescent staining showed that pronounced IL-4 m
240                                              Immunofluorescent staining showed that purinergic recept
241                                              Immunofluorescent staining showed that the collapse of t
242                         Pull-down assays and immunofluorescent staining showed that the major alpha4(
243                                              Immunofluorescent staining showed that wild type TBX5 wa
244                                              Immunofluorescent staining showed that ~50% of endocytos
245                                              Immunofluorescent staining showed the presence of pneumo
246           Combined in situ hybridization and immunofluorescent staining shows that Cblns 1, 2, and 4
247                        We have now performed immunofluorescent-staining studies with four polyclonal
248 ental profiles using electron microscopy and immunofluorescent staining suggest that cell fusions are
249                                              Immunofluorescent staining suggested colocalization of M
250  protein in cells by immunohistochemical and immunofluorescent staining techniques and examined coloc
251 olocalization of endogenous Irgm1, using two immunofluorescent staining techniques, either in fibrobl
252 o only 24 (23.3%) by traditional culture and immunofluorescent-staining techniques.
253                                     Based on immunofluorescent staining, the co-localization of PRC1
254  B and the annexin II tetramer were shown by immunofluorescent staining to colocalize on the surface
255                        Additionally, we used immunofluorescent staining to demonstrate the presence o
256  methods may require the presence of 50,000 (immunofluorescent staining) to 500,000 (AF) oocysts per
257              This expression was verified by immunofluorescent staining using an Ab against axolotl C
258                                              Immunofluorescent staining using anti-EGFR and GFP-ACK1
259 terograde tracing combined with triple label immunofluorescent staining was conducted to examine the
260                                       Direct immunofluorescent staining was done in 200 muL whole-blo
261              Up to now, use of automation in immunofluorescent staining was mostly limited to one mar
262                                         ET-1 immunofluorescent staining was punctate and distinct fro
263                                              Immunofluorescent staining was used to examine junctiona
264                                              Immunofluorescent staining was used to investigate TNF r
265                 Using Western blot, IHC, and immunofluorescent staining, we show persistent factor IX
266 nfocal microscopy (LSCM) in combination with immunofluorescent staining, we simultaneously measured i
267 hanges in MMP protein expression detected by immunofluorescent staining were similar to changes in ge
268                 Real-time RT-PCR, ELISA, and immunofluorescent staining were used to assess the effec
269                              Immunoblots and immunofluorescent staining were used to determine the le
270                                              Immunofluorescent staining with a monoclonal antibody ag
271                                              Immunofluorescent staining with a polyclonal rabbit anti
272                                              Immunofluorescent staining with a specific antibody agai
273                                              Immunofluorescent staining with antibodies to E-cadherin
274 enzyme-linked immunosorbent assay (ELISA) or immunofluorescent staining with confocal laser scanning
275         Using functional assays and specific immunofluorescent staining with multivalent, labeled H-2
276 reen fluorescent protein-tagged proteins and immunofluorescent staining with specific anti-peptide an
277                                              Immunofluorescent staining with specific antibodies immu
278 e sympathetic ganglion neurons by RT-PCR and immunofluorescent staining, with expression occurring be

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