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 the periderm and oral adhe
6 Immunofluorescent analyses showed clear overlap between
7 Immunofluorescent analyses suggested that aberrant traff
8 he percentage of HRPTEC infected with BKV by
immunofluorescent analysis and large T-antigen expressio
9 Immunofluorescent analysis of benign and malignant human
10 By using
immunofluorescent analysis of cerebellar NPCs, we show t
11 Immunofluorescent analysis of clinical samples showed th
12 Immunofluorescent analysis of G(0)/G(1)-enriched or prim
13 Immunofluorescent analysis of isolated myofibers from ne
14 Immunofluorescent analysis of proliferating and tube-for
15 Further flow cytometric and
immunofluorescent analysis showed that in wild-type mice
16 ase chain reaction and globin chain specific
immunofluorescent analysis showed that the cells increas
17 Immunofluorescent analysis suggested that Trp2+ melanocy
18 Fluorescence-activated cell sorter and
immunofluorescent analysis were used to detect binding b
19 in the lung tissue and this was supported by
immunofluorescent analysis.
20 Immunofluorescent and biochemical analysis showed that H
21 otein interaction of STAT3 was analyzed with
immunofluorescent and chromatin immunoprecipitation meth
22 Immunofluorescent and co-immunoprecipitation studies wit
23 ot, and autophagosomes were identified using
immunofluorescent and confocal microscopy.
24 ysis of RNA and protein tissue distribution;
immunofluorescent and electron microscopic examination o
25 In this study,
immunofluorescent and electron-microscopy analyses confi
26 Immunofluorescent and immunoelectron microscopic analyse
27 Confocal
immunofluorescent and immunogold electron microscopy, to
28 Immunofluorescent and immunohistochemical studies for No
29 Utilizing
immunofluorescent and live cell imaging techniques in po
30 RT-PCR for Zika virus, and both microsphere
immunofluorescent and seroneutralisation assays for Zika
31 Using adhesion/invasion assays and
immunofluorescent and transmission electron microscopy,
32 uclear localized, subcellular fractionation,
immunofluorescent,
and electron microscopy revealed both
33 Coimmunoprecipitation,
immunofluorescent,
and electrophysiologic approaches to
34 SG1 to detail the clinical, histopathologic,
immunofluorescent,
and ultrastructural phenotype and to
35 Impression cytology using
immunofluorescent antibodies was performed in 1 individu
36 By the sandwich
immunofluorescent antibody (IFA) method with anti-mouse
37 e tested for microsporidia by using culture,
immunofluorescent antibody, polymerase chain reaction,im
38 inity of the cells, detected with a sandwich
immunofluorescent assay and quantified using a microarra
39 esponses and were positive by the sporozoite
immunofluorescent assay.
40 rs and recipients, 6 serological (4 indirect
immunofluorescent assays [IFA] and 2 enzyme-linked immun
41 In addition,
immunofluorescent assessments of zonula occludens-1 tigh
42 ications gave consistent and clearly defined
immunofluorescent banding patterns.
43 pression levels by an automated quantitative
immunofluorescent-
based technology.
44 r and Purdue) were conducted by cell culture
immunofluorescent (
CCIF) and viral neutralization (VN) a
45 In addition,
immunofluorescent cell count assays showed that while Tr
46 Using thiol labeling strategies and
immunofluorescent cell staining, we found that only 31%
47 An
immunofluorescent cell-based assay was used to evaluate
48 we develop a microscopy approach, multiplex
immunofluorescent cell-based detection of DNA, RNA and P
49 We use a new technique combining
immunofluorescent cell-surface staining and fluorescent
50 luorescent-activated cell sorting (FACS) and
immunofluorescent colocalization studies determined that
51 renol, was subsequently confirmed in situ by
immunofluorescent colocalization studies.
52 Immunofluorescent confocal micrographs demonstrated the
53 Immunofluorescent confocal microscopy demonstrated that
54 n of LNCaP prostate cancer cells, as well as
immunofluorescent confocal microscopy of patient prostat
55 At 48-72 h after HS, electrophysiology and
immunofluorescent confocal microscopy revealed a signifi
56 ells of the retinal inner nuclear layer, and
immunofluorescent confocal microscopy showed that TRPM1
57 In vivo fluorescent fundus imaging and
immunofluorescent confocal microscopy were used for comp
58 pressing ss-galactosidase were determined by
immunofluorescent costaining.
59 A combination of FISH with
immunofluorescent detection of 5-methyl cytosine on supe
60 are found adjacent to synapses in vivo, and
immunofluorescent detection of peptide elongation in acu
61 By using quantitative real-time PCR,
immunofluorescent detection of proteins and enzyme-linke
62 quantified in staphylococcal biofilms using
immunofluorescent detection of pulse-labeled DNA and als
63 ox with Brca1, a driver of HDR, and show via
immunofluorescent detection of repair proteins at ionizi
64 mplification based method of multiple marker
immunofluorescent detection, including detection of anti
65 Immunofluorescent double labeling studies additionally r
66 This was investigated with
immunofluorescent double-labeling techniques to coregist
67 The histopathological, immunohistochemical,
immunofluorescent,
ELISA, and immunoblotting assay resul
68 Before treatment, direct
immunofluorescent examination of a biopsy sample from th
69 Histologic and
immunofluorescent examination showed that double-transge
70 Immunofluorescent histochemistry was employed to detect
71 tion ex vivo MR imaging and bright-field and
immunofluorescent histologic examination were performed.
72 Immunofluorescent histologic findings confirmed the pres
73 Immunofluorescent (
IF) histochemical analysis showed tha
74 Confocal
immunofluorescent images and Western blot analyses of nu
75 However,
immunofluorescent images of B cells infected with fluore
76 Confocal
immunofluorescent images of these cells reveal a predomi
77 ss measurements of 9 and 15 kPa, assessed by
immunofluorescent imaging and quantitation.
78 This finding was confirmed by
immunofluorescent imaging during RBC O2 loading/unloadin
79 Live
immunofluorescent imaging of differentiated osteoblasts
80 Immunofluorescent imaging was used to evaluate Schwann c
81 Using
immunofluorescent imaging, we localized intracellular MM
82 ling kinases was analyzed by Western blot or
immunofluorescent imaging.
83 Reduced EGFR activation was observed using
immunofluorescent imaging.
84 VWF and ET-1
immunofluorescent intensity was similar in young and age
85 g shape parameters of Gamma distributions to
immunofluorescent interfoci distances observed on finite
86 We used immunoperoxidase and
immunofluorescent labeling and stereological counting te
87 e developing and adult C57/BL6 mice brain by
immunofluorescent labeling and Western blotting.
88 Immunofluorescent labeling for: 1) calretinin, 2) calbin
89 Triple
immunofluorescent labeling of boutons contacting motoneu
90 We performed
immunofluorescent labeling of frozen mouse and human liv
91 hagy was measured by immunoblot analyses and
immunofluorescent labeling of LC3.
92 The study used
immunofluorescent labeling of nasal brushings from a dis
93 Immunofluorescent labeling revealed that apoptotic cells
94 orescent in situ hybridization combined with
immunofluorescent labeling revealed that miR-142-3p and
95 NHERF-1(-/-) mouse hepatocytes, although its
immunofluorescent labeling was noticeably weaker.
96 Using double
immunofluorescent labeling we determined that adrenal de
97 Two-photon Ca(2+) imaging, triple
immunofluorescent labeling, and 3D electron microscopic
98 USF81 was confirmed by Western blotting and
immunofluorescent labeling.
99 CLARITY enables
immunofluorescent labelling and imaging of large volumes
100 Immunofluorescent labelling of mitochondria (porin, a vo
101 rrent study, we optimise passive CLARITY and
immunofluorescent labelling of neurons and mitochondrial
102 Immunofluorescent labelling of PKG-Ialpha protein in the
103 Immunofluorescent localisation of RyR protein indicated
104 tious yellows virus (LIYV) by using a unique
immunofluorescent localization approach in which we fed
105 The LHbeta subunit showed a distinct
immunofluorescent localization as compared to the FSHbet
106 Immunofluorescent localization of KORs was determined in
107 e generated, characterized, and used for the
immunofluorescent localization of NRG1 (III) in the deve
108 PRINCIPLE FINDINGS:
Immunofluorescent localization revealed that NTPDase2-po
109 In addition,
immunofluorescent methods demonstrate that P2X labeling
110 aining immunohistochemical and dual-staining
immunofluorescent methods to determine the localization
111 andard histology and immunohistochemical and
immunofluorescent methods were used to analyze lens morp
112 By using
immunofluorescent methods, we determined whether co-infe
113 oclonal antibody for both immunoblotting and
immunofluorescent microscopic analysis.
114 e and after transplantation were examined by
immunofluorescent microscopic assays, and the correlatio
115 ) 10.5 to postnatal (P) and adult stages for
immunofluorescent microscopic studies with antibodies ag
116 ion and adult inflamed corneas were used for
immunofluorescent microscopic studies.
117 ( approximately 8,500 dimers per cell), and
immunofluorescent microscopy (IFM) located MreCD(Spn) to
118 Immunofluorescent microscopy (IFM) showed a change in th
119 sessed in denervated mice versus controls by
immunofluorescent microscopy and real-time PCR.
120 Immunofluorescent microscopy confirmed that MPO added to
121 Immunohistochemical analysis and
immunofluorescent microscopy demonstrated that KSHV infe
122 Consistently, confocal
immunofluorescent microscopy demonstrated that WT RNase
123 t bacterial species was assessed by indirect
immunofluorescent microscopy in each participant.
124 detected by immunoblot analysis and confocal
immunofluorescent microscopy in fibrotic livers from mic
125 TRP120 was observed by
immunofluorescent microscopy in the nucleus of E. chaffe
126 confirmed by Western blot analysis, confocal
immunofluorescent microscopy in vitro, and on cultured o
127 Immunofluorescent microscopy localized PcsB mainly to th
128 Immunofluorescent microscopy of interferon-stimulated CD
129 scence-activated cell sorting (FACS), and by
immunofluorescent microscopy of tissue sections and isol
130 uginosa infection, and (iii) high-resolution
immunofluorescent microscopy to monitor ExoS translocati
131 Immunofluorescent microscopy was used to determine nucle
132 Immunohistochemical analysis and
immunofluorescent microscopy were used to localize and i
133 Western immunoblotting and/or
immunofluorescent microscopy were used to study beta-cat
134 Here, we combined
immunofluorescent microscopy, biochemical assays, in sil
135 We compared three different methods (
immunofluorescent microscopy, IFM; flow cytometry, FCM;
136 iotinylation coupled with immunoblotting and
immunofluorescent microscopy, we assessed the kinetics o
137 Using
immunofluorescent microscopy, we were able to detect NP(
138 tected in infected cells either by RT-PCR or
immunofluorescent microscopy.
139 yuridine, and Hoechst 33342 as visualized by
immunofluorescent microscopy.
140 uten protein structure, using SEM, light and
immunofluorescent microscopy.
141 transcriptase polymerase chain reaction, and
immunofluorescent microscopy.
142 ed macrophages using both immunoblotting and
immunofluorescent microscopy.
143 ent of compound action potentials (CAPs) and
immunofluorescent microscopy.
144 We have assessed a validated quadruple
immunofluorescent OXPHOS (IHC) assay to detect CI defici
145 Immunofluorescent p185(her2/neu) was detected in almost
146 (n = 9) cerebellum as well as developing an
immunofluorescent protocol that consistently labels diff
147 VGAT
immunofluorescent puncta were first seen sparsely in NL
148 smaller than those of BKalpha(+/+) OHCs, and
immunofluorescent quantification showed that efferent pr
149 ue and reached a minimum after 1 h while the
immunofluorescent signal for p-AMPKalpha significantly i
150 tribution of host endothelium to hybrid GBM,
immunofluorescent signals for laminin alpha5 were quanti
151 ed a significant 47% reduction in BK channel
immunofluorescent signals in epileptic rats when compare
152 ISC1, PCM1, and BBS proteins was assessed by
immunofluorescent staining and coimmunoprecipitation.
153 iatric control subjects were used for double
immunofluorescent staining and confocal image analysis.
154 s it in rat NTS by using multiple labels for
immunofluorescent staining and confocal microscopy.
155 identified by the fluorescence "halo" after
immunofluorescent staining and could be retrieved by sit
156 yzed these cells utilizing quantitative-PCR,
immunofluorescent staining and flow cytometry analysis.
157 rculating human EPCs were characterized with
immunofluorescent staining and flow cytometry.
158 We also used
immunofluorescent staining and histology coupled with el
159 tive for (18)F-FMPEP-d2, consistent with the
immunofluorescent staining and in vitro results.
160 Immunofluorescent staining and laser scanning confocal m
161 Using
immunofluorescent staining and live cell imaging of fluo
162 was studied in knockout mice by using double
immunofluorescent staining and real-time polymerase chai
163 MMP14 (MT1-MMP)-haploinsufficient mice using
immunofluorescent staining and scanning electron microsc
164 ed with activated microglia were examined by
immunofluorescent staining and semiquantitative real-tim
165 r the presence of EETs and S aureus by using
immunofluorescent staining and the PNA-Fish assay, respe
166 ssive, confluent clusters as demonstrated by
immunofluorescent staining and TissueFAXS quantitative i
167 HCE cells and corneal epithelium of rats by
immunofluorescent staining and Western blot analysis.
168 nt of jagged-1 in tip cells was confirmed by
immunofluorescent staining as well as by laser capture m
169 By using Northern blot, Western blot, and
immunofluorescent staining assays, we showed that Nur77
170 VE-cadherin
immunofluorescent staining at endothelial AJs and AJ wid
171 Immunofluorescent staining confirmed that SFRP2 and FMO1
172 Immunofluorescent staining confirmed the presence of the
173 Immunofluorescent staining demonstrated microglia activa
174 Immunofluorescent staining demonstrated that administrat
175 Double
immunofluorescent staining demonstrated that Ca(v) 3.3-l
176 Gene expression profiling and
immunofluorescent staining demonstrated that the express
177 Immunofluorescent staining detects overlapping expressio
178 The pattern of
immunofluorescent staining for alpha-SMA and TNC at the
179 Infiltrates were confirmed histologically by
immunofluorescent staining for CD3+ and CD11b+ cells.
180 ht microscopy, including immunohistochemical/
immunofluorescent staining for CD31, CD105, and HMB45, a
181 Combined in situ hybridization and
immunofluorescent staining for CUGBP1 and CUGBP2, the 2
182 Immunofluorescent staining for hexokinase I showed no di
183 ivity was assessed in ATC patient tissues by
immunofluorescent staining for the autophagy marker micr
184 Sequential bindings and
immunofluorescent staining further suggest that 1) TM5 b
185 processes that were prominent in subsequent
immunofluorescent staining images but not with classical
186 us and distinct from ND-10 as defined by PML
immunofluorescent staining in CIN lesions, condylomata,
187 y Western blot and flow cytometry as well as
immunofluorescent staining in primary sinus epithelial c
188 In this study, Xin was analyzed by
immunofluorescent staining in skeletal muscle samples fr
189 polymerase chain reaction in total liver and
immunofluorescent staining in tissues for synaptophysin
190 Double-
immunofluorescent staining indicated that the majority o
191 Immunofluorescent staining is an informative tool that i
192 Immunofluorescent staining of alpha-actin revealed that
193 Endothelial cell culture and preliminary
immunofluorescent staining of Anaplasma-infected tissues
194 Immunofluorescent staining of both whole bladder tissue
195 TER measurement and
immunofluorescent staining of cadherins after a calcium
196 cell and TM cell markers were identified by
immunofluorescent staining of cryosections or tissue who
197 a possible defect in the centromeric region,
immunofluorescent staining of cyclin A1 protein shows lo
198 Consistent with these findings,
immunofluorescent staining of fast but not slow muscle m
199 mission electron microscopy of glomeruli and
immunofluorescent staining of glomerular epithelial cell
200 by replacing ClO(-) with SP in vivo, and by
immunofluorescent staining of large airways of exposed m
201 Immunofluorescent staining of lumbar DRG demonstrated th
202 Immunofluorescent staining of markers for activated endo
203 Biochemical fractionation studies and
immunofluorescent staining of murine brain slices reveal
204 Histology and
immunofluorescent staining of PKC and epidermal growth f
205 Indirect
immunofluorescent staining of SCC cryosections and Weste
206 ocal microscopy provided cross validation by
immunofluorescent staining of the compartments.
207 Immunofluorescent staining of tumour sections from human
208 Notably,
immunofluorescent staining of viral proteins revealed an
209 Immunofluorescent staining on testis sections with the m
210 Both antisera gave the same distinctive
immunofluorescent staining pattern, with unstained heter
211 Mitogenic activation and
immunofluorescent staining performed inside the microflu
212 tabase including the addition of subcellular
immunofluorescent staining results from the Human Protei
213 of MALDI-IMS data with subsequently acquired
immunofluorescent staining results.
214 Double
immunofluorescent staining revealed a co-expression of W
215 Surprisingly,
immunofluorescent staining revealed a cytoplasmic misloc
216 Immunofluorescent staining revealed a dynamic ECM remode
217 However,
immunofluorescent staining revealed an increased frequen
218 Immunofluorescent staining revealed constitutive and ind
219 Immunofluorescent staining revealed impairment of photor
220 Immunofluorescent staining revealed localization of the
221 Immunofluorescent staining revealed reduced surface expr
222 Immunofluorescent staining revealed the presence of STAT
223 Immunohistochemical and
immunofluorescent staining show that ODN treatment drama
224 ampal degeneration in C57BL/6 mice, in which
immunofluorescent staining showed a 28% loss of PSD95-po
225 Immunofluorescent staining showed a significant reductio
226 Double
immunofluorescent staining showed aberrant co-localizati
227 In addition, double
immunofluorescent staining showed co-localization of end
228 Immunofluorescent staining showed higher numbers of CD31
229 l populations in lung tissue cryosections by
immunofluorescent staining showed sparse bacteria within
230 Immunofluorescent staining showed that Panx1 expression
231 Laser capture microdissection and
immunofluorescent staining showed that pronounced IL-4 m
232 Immunofluorescent staining showed that ~50% of endocytos
233 Immunofluorescent staining showed the presence of pneumo
234 Combined in situ hybridization and
immunofluorescent staining shows that Cblns 1, 2, and 4
235 olocalization of endogenous Irgm1, using two
immunofluorescent staining techniques, either in fibrobl
236 Additionally, we used
immunofluorescent staining to demonstrate the presence o
237 Direct
immunofluorescent staining was done in 200 muL whole-blo
238 Up to now, use of automation in
immunofluorescent staining was mostly limited to one mar
239 ET-1
immunofluorescent staining was punctate and distinct fro
240 Real-time RT-PCR, ELISA, and
immunofluorescent staining were used to assess the effec
241 enzyme-linked immunosorbent assay (ELISA) or
immunofluorescent staining with confocal laser scanning
242 reen fluorescent protein-tagged proteins and
immunofluorescent staining with specific anti-peptide an
243 aracterized by hyperphosphorylated tau (AT8;
immunofluorescent staining) pathological inclusions, neu
244 ings were corroborated by electrophysiology,
immunofluorescent staining, and biotinylation of surface
245 ed by using RT-PCR, ELISA, Western blotting,
immunofluorescent staining, and flow cytometry.
246 ive polymerase chain reaction, dual-labeling
immunofluorescent staining, and immunoassays.
247 f RIP1 was monitored by reporter gene assay,
immunofluorescent staining, and Western blotting.
248 safety of this treatment were examined using
immunofluorescent staining, confocal imaging, immunoelec
249 Flow cytometry,
immunofluorescent staining, confocal microscopy, and ana
250 By combining
immunofluorescent staining, fluorescence in situ hybridi
251 ns could be simultaneously isolated and, via
immunofluorescent staining, individually identified and
252 g qRT-PCR, immunoprecipitation/Western blot,
immunofluorescent staining, radio-thin-layer chromatogra
253 Based on
immunofluorescent staining, the co-localization of PRC1
254 Using Western blot, IHC, and
immunofluorescent staining, we show persistent factor IX
255 e sympathetic ganglion neurons by RT-PCR and
immunofluorescent staining, with expression occurring be
256 by quantitative PCR (qPCR), immunoblots, and
immunofluorescent staining.
257 rn blot and of protein expression by IHC and
immunofluorescent staining.
258 e, HBx-mSin3A colocalization was detected by
immunofluorescent staining.
259 transplantation model by flow cytometry and
immunofluorescent staining.
260 e contrast agent (Eu-P947) with specific MMP
immunofluorescent staining.
261 ong the z axis, as well as depth-independent
immunofluorescent staining.
262 ity of CR-1 by fluorescent cell-labeling and
immunofluorescent staining.
263 ectin (FN) was monitored by Western blot and
immunofluorescent staining.
264 d by ELISA, zymography, Western blotting and
immunofluorescent staining.
265 tic fibers in ONH tissue was investigated by
immunofluorescent staining.
266 stained for CB1 and uncoupling protein-1 by
immunofluorescent staining.
267 ugated dextran, and (ii) AJC structure using
immunofluorescent staining.
268 o only 24 (23.3%) by traditional culture and
immunofluorescent-
staining techniques.
269 Immunofluorescent stainings demonstrated localization to
270 This was addressed by immunohistochemical/
immunofluorescent stainings performed on grafted tissue
271 series of postmortem immunohistochemical and
immunofluorescent stainings, as well as Western blot ana
272 lular localization of FKBP10 was assessed by
immunofluorescent stainings.
273 detection of the organism by colorimetric or
immunofluorescent stains or by polymerase chain reaction
274 Immunofluorescent studies demonstrate perinuclear coloca
275 Co-immunoprecipitation and
immunofluorescent studies demonstrated that PIDD-CC, RAI
276 Immunofluorescent studies demonstrated that the aggregat
277 transfected mutant protein function by using
immunofluorescent studies in Hep-2 cells; quantitation o
278 Immunofluorescent studies on HEK293 cells coexpressing b
279 Immunofluorescent studies on mouse biopsies treated with
280 Immunofluorescent studies revealed colocalization of TIN
281 Immunofluorescent studies revealed complex coexpression
282 Immunofluorescent studies showed that CXCR4 was co-expre
283 Immunofluorescent studies suggested that HDL promoted TR
284 Histopathologic, electron microscopy, and
immunofluorescent studies were performed.
285 -linked immunosorbent assay and quantitative
immunofluorescent studies.
286 es in disease, we have developed a quadruple
immunofluorescent technique enabling the quantification
287 ical techniques and immunohistochemistry and
immunofluorescent technique.
288 Immunofluorescent techniques were used to stain for new
289 Gliosis was evaluated by
immunofluorescent techniques.
290 different light conditions was determined by
immunofluorescent techniques.
291 the most common findings observed on direct
immunofluorescent testing in patients with mucous membra
292 Biopsy with direct
immunofluorescent testing is essential to confirm the di
293 Additionally, Western blotting and
immunofluorescent tissue staining were used to analyse t
294 osed to desiccating stress were evaluated by
immunofluorescent tomography and 3-dimensional reconstru
295 echanism of NPAS3 etiopathology, we combined
immunofluorescent,
transcriptomic and metabonomic approa
296 ol for rapid, three-dimensional, multiplexed
immunofluorescent tumor imaging.
297 Confocal microscopic analysis of
immunofluorescent UT-A1 and snapin showed co-localizatio
298 ne layers, which appear to coincide with the
immunofluorescent VIPP1 spots and suggest a defect in th
299 Hypoxia was detected by
immunofluorescent visualization of pimonidazole and the
300 male brown anole lizard, Anolis sagrei, via
immunofluorescent visualization of the rate-limiting enz