1 Immunofluorescent analyses demonstrated that both excita
2 Immunofluorescent analyses following FGF23 injection in
3 We performed immunohistochemical and
immunofluorescent analyses of 116 colorectal tumor biops
4 Immunohistochemical and
immunofluorescent analyses of a matched breast cancer pr
5 Immunofluorescent analyses of fibrotic kidney tissue ide
6 Immunofluorescent analyses of the periderm and oral adhe
7 Immunofluorescent analyses showed clear overlap between
8 Immunofluorescent analyses suggested that aberrant traff
9 he percentage of HRPTEC infected with BKV by
immunofluorescent analysis and large T-antigen expressio
10 Immunofluorescent analysis of benign and malignant human
11 By using
immunofluorescent analysis of cerebellar NPCs, we show t
12 Immunofluorescent analysis of clinical samples showed th
13 Immunofluorescent analysis of G(0)/G(1)-enriched or prim
14 Immunofluorescent analysis of isolated myofibers from ne
15 ase chain reaction and globin chain specific
immunofluorescent analysis showed that the cells increas
16 Immunofluorescent analysis showed the presence of the pr
17 Immunofluorescent analysis suggested that Trp2+ melanocy
18 Fluorescence-activated cell sorter and
immunofluorescent analysis were used to detect binding b
19 Immunofluorescent and biochemical analysis showed that H
20 otein interaction of STAT3 was analyzed with
immunofluorescent and chromatin immunoprecipitation meth
21 Immunofluorescent and co-immunoprecipitation studies wit
22 ot, and autophagosomes were identified using
immunofluorescent and confocal microscopy.
23 ysis of RNA and protein tissue distribution;
immunofluorescent and electron microscopic examination o
24 In this study,
immunofluorescent and electron-microscopy analyses confi
25 Immunofluorescent and immunoelectron microscopic analyse
26 Confocal
immunofluorescent and immunogold electron microscopy, to
27 Immunofluorescent and immunohistochemical studies for No
28 Utilizing
immunofluorescent and live cell imaging techniques in po
29 RT-PCR for Zika virus, and both microsphere
immunofluorescent and seroneutralisation assays for Zika
30 Using adhesion/invasion assays and
immunofluorescent and transmission electron microscopy,
31 Coimmunoprecipitation,
immunofluorescent,
and electrophysiologic approaches to
32 SG1 to detail the clinical, histopathologic,
immunofluorescent,
and ultrastructural phenotype and to
33 Impression cytology using
immunofluorescent antibodies was performed in 1 individu
34 e tested for microsporidia by using culture,
immunofluorescent antibody, polymerase chain reaction,im
35 Due to the poor sensitivity of
immunofluorescent-
antibody assays (IFAs), a reliable ser
36 Biochemical and
immunofluorescent approaches were used to dissect AnxA6(
37 We used
immunofluorescent array tomography to quantify different
38 inity of the cells, detected with a sandwich
immunofluorescent assay and quantified using a microarra
39 a-Levitt et al., chemical screening using an
immunofluorescent assay identified a compound that cause
40 esponses and were positive by the sporozoite
immunofluorescent assay.
41 rs and recipients, 6 serological (4 indirect
immunofluorescent assays [IFA] and 2 enzyme-linked immun
42 In addition,
immunofluorescent assessments of zonula occludens-1 tigh
43 s revealed a combination of large, intensely
immunofluorescent axons in myenteric plexus and circular
44 ications gave consistent and clearly defined
immunofluorescent banding patterns.
45 pression levels by an automated quantitative
immunofluorescent-
based technology.
46 Automated Screening Tool for Dosimetry), an
immunofluorescent,
biomarker-based system designed to re
47 r and Purdue) were conducted by cell culture
immunofluorescent (
CCIF) and viral neutralization (VN) a
48 In addition,
immunofluorescent cell count assays showed that while Tr
49 Using thiol labeling strategies and
immunofluorescent cell staining, we found that only 31%
50 An
immunofluorescent cell-based assay was used to evaluate
51 we develop a microscopy approach, multiplex
immunofluorescent cell-based detection of DNA, RNA and P
52 We use a new technique combining
immunofluorescent cell-surface staining and fluorescent
53 luorescent-activated cell sorting (FACS) and
immunofluorescent colocalization studies determined that
54 renol, was subsequently confirmed in situ by
immunofluorescent colocalization studies.
55 Immunofluorescent confocal micrographs demonstrated the
56 n of LNCaP prostate cancer cells, as well as
immunofluorescent confocal microscopy of patient prostat
57 At 48-72 h after HS, electrophysiology and
immunofluorescent confocal microscopy revealed a signifi
58 ells of the retinal inner nuclear layer, and
immunofluorescent confocal microscopy showed that TRPM1
59 um imaging with quantitative immunoblotting,
immunofluorescent confocal microscopy, and balance studi
60 pressing ss-galactosidase were determined by
immunofluorescent costaining.
61 To address this notable gap, we used
immunofluorescent cytology to quantify genome-wide recom
62 A combination of FISH with
immunofluorescent detection of 5-methyl cytosine on supe
63 are found adjacent to synapses in vivo, and
immunofluorescent detection of peptide elongation in acu
64 quantified in staphylococcal biofilms using
immunofluorescent detection of pulse-labeled DNA and als
65 ox with Brca1, a driver of HDR, and show via
immunofluorescent detection of repair proteins at ionizi
66 mplification based method of multiple marker
immunofluorescent detection, including detection of anti
67 This was investigated with
immunofluorescent double-labeling techniques to coregist
68 The histopathological, immunohistochemical,
immunofluorescent,
ELISA, and immunoblotting assay resul
69 Before treatment, direct
immunofluorescent examination of a biopsy sample from th
70 Histologic and
immunofluorescent examination showed that double-transge
71 Immunofluorescent histochemistry was employed to detect
72 tion ex vivo MR imaging and bright-field and
immunofluorescent histologic examination were performed.
73 Immunofluorescent histologic findings confirmed the pres
74 Immunofluorescent (
IF) histochemical analysis showed tha
75 Confocal
immunofluorescent images and Western blot analyses of nu
76 However,
immunofluorescent images of B cells infected with fluore
77 Confocal
immunofluorescent images of these cells reveal a predomi
78 ss measurements of 9 and 15 kPa, assessed by
immunofluorescent imaging and quantitation.
79 This finding was confirmed by
immunofluorescent imaging during RBC O2 loading/unloadin
80 Live
immunofluorescent imaging of differentiated osteoblasts
81 Immunofluorescent imaging was used to evaluate Schwann c
82 Using
immunofluorescent imaging, we localized intracellular MM
83 ling kinases was analyzed by Western blot or
immunofluorescent imaging.
84 Reduced EGFR activation was observed using
immunofluorescent imaging.
85 VWF and ET-1
immunofluorescent intensity was similar in young and age
86 g shape parameters of Gamma distributions to
immunofluorescent interfoci distances observed on finite
87 eurons and glia were also investigated using
immunofluorescent labeling and correlated to serum level
88 We used immunoperoxidase and
immunofluorescent labeling and stereological counting te
89 e developing and adult C57/BL6 mice brain by
immunofluorescent labeling and Western blotting.
90 Immunofluorescent labeling for: 1) calretinin, 2) calbin
91 Triple
immunofluorescent labeling of boutons contacting motoneu
92 We performed
immunofluorescent labeling of frozen mouse and human liv
93 hagy was measured by immunoblot analyses and
immunofluorescent labeling of LC3.
94 The study used
immunofluorescent labeling of nasal brushings from a dis
95 Immunofluorescent labeling revealed that apoptotic cells
96 orescent in situ hybridization combined with
immunofluorescent labeling revealed that miR-142-3p and
97 NHERF-1(-/-) mouse hepatocytes, although its
immunofluorescent labeling was noticeably weaker.
98 Using double
immunofluorescent labeling we determined that adrenal de
99 Two-photon Ca(2+) imaging, triple
immunofluorescent labeling, and 3D electron microscopic
100 Using
immunofluorescent labeling, flow cytometry and Cre-depen
101 USF81 was confirmed by Western blotting and
immunofluorescent labeling.
102 CLARITY enables
immunofluorescent labelling and imaging of large volumes
103 aring ones, showed decreased chromogenic and
immunofluorescent labelling in AD in every cortical laye
104 Immunofluorescent labelling of mitochondria (porin, a vo
105 rrent study, we optimise passive CLARITY and
immunofluorescent labelling of neurons and mitochondrial
106 Immunofluorescent labelling of PKG-Ialpha protein in the
107 Cell types were confirmed with double
immunofluorescent labelling.
108 Immunofluorescent localisation of RyR protein indicated
109 tious yellows virus (LIYV) by using a unique
immunofluorescent localization approach in which we fed
110 The LHbeta subunit showed a distinct
immunofluorescent localization as compared to the FSHbet
111 Immunofluorescent localization of KORs was determined in
112 e generated, characterized, and used for the
immunofluorescent localization of NRG1 (III) in the deve
113 PRINCIPLE FINDINGS:
Immunofluorescent localization revealed that NTPDase2-po
114 In addition,
immunofluorescent methods demonstrate that P2X labeling
115 aining immunohistochemical and dual-staining
immunofluorescent methods to determine the localization
116 andard histology and immunohistochemical and
immunofluorescent methods were used to analyze lens morp
117 oclonal antibody for both immunoblotting and
immunofluorescent microscopic analysis.
118 e and after transplantation were examined by
immunofluorescent microscopic assays, and the correlatio
119 ) 10.5 to postnatal (P) and adult stages for
immunofluorescent microscopic studies with antibodies ag
120 ion and adult inflamed corneas were used for
immunofluorescent microscopic studies.
121 ( approximately 8,500 dimers per cell), and
immunofluorescent microscopy (IFM) located MreCD(Spn) to
122 Immunofluorescent microscopy (IFM) showed a change in th
123 sessed in denervated mice versus controls by
immunofluorescent microscopy and real-time PCR.
124 Immunohistochemical analysis and
immunofluorescent microscopy demonstrated that KSHV infe
125 Consistently, confocal
immunofluorescent microscopy demonstrated that WT RNase
126 detected by immunoblot analysis and confocal
immunofluorescent microscopy in fibrotic livers from mic
127 TRP120 was observed by
immunofluorescent microscopy in the nucleus of E. chaffe
128 Immunofluorescent microscopy localized PcsB mainly to th
129 Immunofluorescent microscopy of interferon-stimulated CD
130 scence-activated cell sorting (FACS), and by
immunofluorescent microscopy of tissue sections and isol
131 Immunofluorescent microscopy showed that HBs proteins, i
132 uginosa infection, and (iii) high-resolution
immunofluorescent microscopy to monitor ExoS translocati
133 Immunofluorescent microscopy was used to determine nucle
134 Immunohistochemical analysis and
immunofluorescent microscopy were used to localize and i
135 Western immunoblotting and/or
immunofluorescent microscopy were used to study beta-cat
136 Here, we combined
immunofluorescent microscopy, biochemical assays, in sil
137 We compared three different methods (
immunofluorescent microscopy, IFM; flow cytometry, FCM;
138 iotinylation coupled with immunoblotting and
immunofluorescent microscopy, we assessed the kinetics o
139 Using
immunofluorescent microscopy, we were able to detect NP(
140 and changes in HA receptor expression using
immunofluorescent microscopy.
141 tected in infected cells either by RT-PCR or
immunofluorescent microscopy.
142 yuridine, and Hoechst 33342 as visualized by
immunofluorescent microscopy.
143 uten protein structure, using SEM, light and
immunofluorescent microscopy.
144 +) and NG2(+)) were analyzed via whole mount
immunofluorescent microscopy.
145 ed macrophages using both immunoblotting and
immunofluorescent microscopy.
146 ent of compound action potentials (CAPs) and
immunofluorescent microscopy.
147 We have assessed a validated quadruple
immunofluorescent OXPHOS (IHC) assay to detect CI defici
148 Immunofluorescent p185(her2/neu) was detected in almost
149 (n = 9) cerebellum as well as developing an
immunofluorescent protocol that consistently labels diff
150 VGAT
immunofluorescent puncta were first seen sparsely in NL
151 smaller than those of BKalpha(+/+) OHCs, and
immunofluorescent quantification showed that efferent pr
152 ue and reached a minimum after 1 h while the
immunofluorescent signal for p-AMPKalpha significantly i
153 ed a significant 47% reduction in BK channel
immunofluorescent signals in epileptic rats when compare
154 ISC1, PCM1, and BBS proteins was assessed by
immunofluorescent staining and coimmunoprecipitation.
155 iatric control subjects were used for double
immunofluorescent staining and confocal image analysis.
156 identified by the fluorescence "halo" after
immunofluorescent staining and could be retrieved by sit
157 Immunofluorescent staining and FACS analysis show that A
158 Immunofluorescent staining and flow cytometric analyses
159 rculating human EPCs were characterized with
immunofluorescent staining and flow cytometry.
160 We also used
immunofluorescent staining and histology coupled with el
161 tive for (18)F-FMPEP-d2, consistent with the
immunofluorescent staining and in vitro results.
162 Immunofluorescent staining and laser scanning confocal m
163 Using
immunofluorescent staining and live cell imaging of fluo
164 n B-CLL clones and approaches involving both
immunofluorescent staining and pharmacologic inhibitors,
165 was studied in knockout mice by using double
immunofluorescent staining and real-time polymerase chai
166 MMP14 (MT1-MMP)-haploinsufficient mice using
immunofluorescent staining and scanning electron microsc
167 ed with activated microglia were examined by
immunofluorescent staining and semiquantitative real-tim
168 r the presence of EETs and S aureus by using
immunofluorescent staining and the PNA-Fish assay, respe
169 ssive, confluent clusters as demonstrated by
immunofluorescent staining and TissueFAXS quantitative i
170 HCE cells and corneal epithelium of rats by
immunofluorescent staining and Western blot analysis.
171 nt of jagged-1 in tip cells was confirmed by
immunofluorescent staining as well as by laser capture m
172 By using Northern blot, Western blot, and
immunofluorescent staining assays, we showed that Nur77
173 VE-cadherin
immunofluorescent staining at endothelial AJs and AJ wid
174 In vitro
immunofluorescent staining confirmed that hDPSCs express
175 Immunofluorescent staining confirmed that SFRP2 and FMO1
176 experiments, proximity ligation assays, and
immunofluorescent staining confirmed the interaction bet
177 Immunofluorescent staining confirmed the presence of the
178 Immunofluorescent staining demonstrated microglia activa
179 Immunofluorescent staining demonstrated that administrat
180 Double
immunofluorescent staining demonstrated that Ca(v) 3.3-l
181 Gene expression profiling and
immunofluorescent staining demonstrated that the express
182 Immunofluorescent staining detects overlapping expressio
183 The pattern of
immunofluorescent staining for alpha-SMA and TNC at the
184 Infiltrates were confirmed histologically by
immunofluorescent staining for CD3+ and CD11b+ cells.
185 ht microscopy, including immunohistochemical/
immunofluorescent staining for CD31, CD105, and HMB45, a
186 ivity was assessed in ATC patient tissues by
immunofluorescent staining for the autophagy marker micr
187 Ex vivo
immunofluorescent staining for TSPO and CD68 (macrophage
188 Sequential bindings and
immunofluorescent staining further suggest that 1) TM5 b
189 processes that were prominent in subsequent
immunofluorescent staining images but not with classical
190 us and distinct from ND-10 as defined by PML
immunofluorescent staining in CIN lesions, condylomata,
191 y Western blot and flow cytometry as well as
immunofluorescent staining in primary sinus epithelial c
192 In this study, Xin was analyzed by
immunofluorescent staining in skeletal muscle samples fr
193 polymerase chain reaction in total liver and
immunofluorescent staining in tissues for synaptophysin
194 Double-
immunofluorescent staining indicated that the majority o
195 Immunofluorescent staining is an informative tool that i
196 Immunofluorescent staining of alpha-actin revealed that
197 Endothelial cell culture and preliminary
immunofluorescent staining of Anaplasma-infected tissues
198 Immunofluorescent staining of both whole bladder tissue
199 TER measurement and
immunofluorescent staining of cadherins after a calcium
200 cell and TM cell markers were identified by
immunofluorescent staining of cryosections or tissue who
201 Immunofluorescent staining of E-cadherin and EdU reveale
202 re authenticated by CD31 immunoblotting, and
immunofluorescent staining of established EC markers VE-
203 Consistent with these findings,
immunofluorescent staining of fast but not slow muscle m
204 mission electron microscopy of glomeruli and
immunofluorescent staining of glomerular epithelial cell
205 by replacing ClO(-) with SP in vivo, and by
immunofluorescent staining of large airways of exposed m
206 Immunofluorescent staining of markers for activated endo
207 Biochemical fractionation studies and
immunofluorescent staining of murine brain slices reveal
208 Histology and
immunofluorescent staining of PKC and epidermal growth f
209 By using
immunofluorescent staining of the c-Fos-positive neurons
210 ocal microscopy provided cross validation by
immunofluorescent staining of the compartments.
211 Immunofluorescent staining of tumour sections from human
212 Notably,
immunofluorescent staining of viral proteins revealed an
213 Immunofluorescent staining on testis sections with the m
214 Both antisera gave the same distinctive
immunofluorescent staining pattern, with unstained heter
215 Mitogenic activation and
immunofluorescent staining performed inside the microflu
216 tabase including the addition of subcellular
immunofluorescent staining results from the Human Protei
217 of MALDI-IMS data with subsequently acquired
immunofluorescent staining results.
218 Double
immunofluorescent staining revealed a co-expression of W
219 Surprisingly,
immunofluorescent staining revealed a cytoplasmic misloc
220 Immunofluorescent staining revealed a dynamic ECM remode
221 However,
immunofluorescent staining revealed an increased frequen
222 Immunofluorescent staining revealed constitutive and ind
223 Immunofluorescent staining revealed impairment of photor
224 Immunofluorescent staining revealed localization of the
225 Immunofluorescent staining revealed reduced surface expr
226 Immunohistochemical and
immunofluorescent staining show that ODN treatment drama
227 ampal degeneration in C57BL/6 mice, in which
immunofluorescent staining showed a 28% loss of PSD95-po
228 Immunofluorescent staining showed a significant reductio
229 Double
immunofluorescent staining showed aberrant co-localizati
230 In addition, double
immunofluorescent staining showed co-localization of end
231 Immunofluorescent staining showed higher numbers of CD31
232 l populations in lung tissue cryosections by
immunofluorescent staining showed sparse bacteria within
233 Immunofluorescent staining showed that Panx1 expression
234 Immunofluorescent staining showed that ~50% of endocytos
235 Immunofluorescent staining showed the presence of pneumo
236 Combined in situ hybridization and
immunofluorescent staining shows that Cblns 1, 2, and 4
237 olocalization of endogenous Irgm1, using two
immunofluorescent staining techniques, either in fibrobl
238 Additionally, we used
immunofluorescent staining to demonstrate the presence o
239 Direct
immunofluorescent staining was done in 200 muL whole-blo
240 Up to now, use of automation in
immunofluorescent staining was mostly limited to one mar
241 ET-1
immunofluorescent staining was punctate and distinct fro
242 Real-time RT-PCR, ELISA, and
immunofluorescent staining were used to assess the effec
243 enzyme-linked immunosorbent assay (ELISA) or
immunofluorescent staining with confocal laser scanning
244 aracterized by hyperphosphorylated tau (AT8;
immunofluorescent staining) pathological inclusions, neu
245 ings were corroborated by electrophysiology,
immunofluorescent staining, and biotinylation of surface
246 ed by using RT-PCR, ELISA, Western blotting,
immunofluorescent staining, and flow cytometry.
247 ive polymerase chain reaction, dual-labeling
immunofluorescent staining, and immunoassays.
248 f RIP1 was monitored by reporter gene assay,
immunofluorescent staining, and Western blotting.
249 safety of this treatment were examined using
immunofluorescent staining, confocal imaging, immunoelec
250 Flow cytometry,
immunofluorescent staining, confocal microscopy, and ana
251 By combining
immunofluorescent staining, fluorescence in situ hybridi
252 ns could be simultaneously isolated and, via
immunofluorescent staining, individually identified and
253 g qRT-PCR, immunoprecipitation/Western blot,
immunofluorescent staining, radio-thin-layer chromatogra
254 Based on
immunofluorescent staining, the co-localization of PRC1
255 Using Western blot, IHC, and
immunofluorescent staining, we show persistent factor IX
256 e sympathetic ganglion neurons by RT-PCR and
immunofluorescent staining, with expression occurring be
257 ugated dextran, and (ii) AJC structure using
immunofluorescent staining.
258 e the expression of senescence biomarkers by
immunofluorescent staining.
259 eration in mutant epithelium, as revealed by
immunofluorescent staining.
260 IL-15, as indicated by Western blotting and
immunofluorescent staining.
261 by quantitative PCR (qPCR), immunoblots, and
immunofluorescent staining.
262 rn blot and of protein expression by IHC and
immunofluorescent staining.
263 e, HBx-mSin3A colocalization was detected by
immunofluorescent staining.
264 valuated using qRT-PCR, western blotting and
immunofluorescent staining.
265 transplantation model by flow cytometry and
immunofluorescent staining.
266 d of osteoprotegerin (OPG) were evaluated by
immunofluorescent staining.
267 e contrast agent (Eu-P947) with specific MMP
immunofluorescent staining.
268 ong the z axis, as well as depth-independent
immunofluorescent staining.
269 d by ELISA, zymography, Western blotting and
immunofluorescent staining.
270 stained for CB1 and uncoupling protein-1 by
immunofluorescent staining.
271 o only 24 (23.3%) by traditional culture and
immunofluorescent-
staining techniques.
272 Immunofluorescent stainings demonstrated localization to
273 This was addressed by immunohistochemical/
immunofluorescent stainings performed on grafted tissue
274 series of postmortem immunohistochemical and
immunofluorescent stainings, as well as Western blot ana
275 lular localization of FKBP10 was assessed by
immunofluorescent stainings.
276 detection of the organism by colorimetric or
immunofluorescent stains or by polymerase chain reaction
277 Co-immunoprecipitation and
immunofluorescent studies demonstrated that PIDD-CC, RAI
278 Immunofluorescent studies demonstrated that the aggregat
279 transfected mutant protein function by using
immunofluorescent studies in Hep-2 cells; quantitation o
280 Immunofluorescent studies on HEK293 cells coexpressing b
281 Immunofluorescent studies on mouse biopsies treated with
282 Immunofluorescent studies revealed colocalization of TIN
283 Immunofluorescent studies revealed complex coexpression
284 Immunofluorescent studies showed that CXCR4 was co-expre
285 Immunofluorescent studies suggested that HDL promoted TR
286 Histopathologic, electron microscopy, and
immunofluorescent studies were performed.
287 -linked immunosorbent assay and quantitative
immunofluorescent studies.
288 es in disease, we have developed a quadruple
immunofluorescent technique enabling the quantification
289 ical techniques and immunohistochemistry and
immunofluorescent technique.
290 Immunofluorescent techniques were used to stain for new
291 Gliosis was evaluated by
immunofluorescent techniques.
292 the most common findings observed on direct
immunofluorescent testing in patients with mucous membra
293 Biopsy with direct
immunofluorescent testing is essential to confirm the di
294 Additionally, Western blotting and
immunofluorescent tissue staining were used to analyse t
295 osed to desiccating stress were evaluated by
immunofluorescent tomography and 3-dimensional reconstru
296 echanism of NPAS3 etiopathology, we combined
immunofluorescent,
transcriptomic and metabonomic approa
297 g-based method called speedy histological-to-
immunofluorescent translation (SHIFT) which takes histol
298 ol for rapid, three-dimensional, multiplexed
immunofluorescent tumor imaging.
299 ne layers, which appear to coincide with the
immunofluorescent VIPP1 spots and suggest a defect in th
300 male brown anole lizard, Anolis sagrei, via
immunofluorescent visualization of the rate-limiting enz