ライフサイエンスコーパス: FITC

1 FITC-albumin, Lsr-F, or fluorescent polystyrene latex pa

2 FITC-D weighing up to 70-kDa, as well as NaF, reached th

3 FITC-dextran molecules were chosen as models of migrant

4 FITC-dextran-perfused retinas exhibited prominent neovas

5 FITC-labeled aptamer was used as a binder molecule in th

6 FITC-PNA-Antp accumulates in nuclei of keratinocytes, an

7 FITC-tagged proteins were purified from a contaminant pr

8 FITC-TrapG was selectively trapped on purified beta-gluc

9 G6-5aSlex-FITC conjugate could specifically capture HT29 cells eve

10 G6-5aSlex-FITC conjugate showed capture efficiency better than FIT

11 fluorescein (376Da) and weakly anionic 70kDa FITC-dextran), probe concentration (50 to 200 ppm), and

12 BBB permeability to 70kDa FITC-Dextran was measured 24h following injury and quant

13 matic cleavage of SA and by staining using a FITC labeled SA selective lectin.

14 iocyanate labeled 3-aminophenylboronic acid (FITC-APBA) as the chemoselective recognition probe of si

15 ((4-(dimethylamino)phenyl)azo) benzoic acid (FITC/DABCYL) FRET pair to produce a signal upon substrat

16 beta-glucuronidase-activated FITC-TrapG did not interfere with beta-glucuronidase act

17 the half-life of intravenously administered FITC-sinistrin, a molecule cleared by glomerular filtrat

18 the cGMP analog 8-bromo-cGMP did not affect FITC-insulin uptake.

19 DLN contained twice more fluorescence after FITC skin painting and twice more donor DC after footpad

20 Moreover, after FITC application the appearance of hapten-laden LCs (FIT

21 capsulated fluorescent-bovine serum albumin (FITC-BSA) inside the gel.

22 ed by analyzing 100 nm liposomes and albumin-FITC conjugate.

23 less than 6 min, about 10 min before albumin-FITC.

24 llophycocyanin (APC)-conjugated PDGFR-alpha, FITC-conjugated Sca-1, phycoerythrin (PE)-conjugated CD4

25 An FITC-labeled analogue of this polyamide can be detected

26 O mice compared with WT mice (P < 0.001) and FITC-dextran permeability assay suggested a higher exten

27 ing SYTO, DAPI dilactate, Hoechst 33342, and FITC dyes upon the pheochromocytoma PC-12 cells and RAW

28 xed, incubated with anti-biotin antibody and FITC-labeled goat anti-mouse antibody, and examined unde

29 fluorescent molecules, sulforhodamine-B and FITC-insulin in vitro, and absorption enhancement of sal

30 calization of MitoTracker Red at 2 hours and FITC -p b-sCD44 was 17.4% (P < 0.001) and for FITC b-sCD

31 the ratio of bound and free Cy5-insulin and FITC-glucagon in the presence of their respective antibo

32 There was minimal penetration of NaF and FITC-D into the mid-vitreous in the in vivo experiments.

33 C insulin-stimulated Akt phosphorylation and FITC-insulin uptake that was partially reversed by SNP i

34 hree different fluorophores 2-AP, POPOP, and FITC, respectively.

35 via hemolysis, cell viability, and AnnexinV-FITC/PI staining assays.

36 Anti-FITC-CAR-T cell activation and proliferation was strictl

37 ing using Fab fragments of anti-Dig and anti-FITC conjugated to peroxidase or alkaline phosphatase, r

38 pressing cancer cells and a "universal" anti-FITC-directed CAR-T cell.

39 the cytoplasmic headpiece, thereby assigning FITC-SERCA as a nucleotide-free enzyme.

40 MMP-2 inhibitor, reduced pericyte-associated FITC-gelatin fluorescence and plasma leakage.

41 ength excitation, FITC/BSA-stabilized AuNCs (FITC/BSA-AuNCs) emitted fluorescence at 525 and 670nm, w

42 ein isothiocyanate (FITC)-labeled avidin (Av-FITC) as the template.

43 "on-the-fly" extraction and isolation of Av-FITC from raw serum and saliva samples along with real-t

44 s superior to that of commercially available FITC-antibody probe.

45 mulatory function of skin-derived Ag-bearing FITC(+)CD11c(+) dendritic cells in draining lymph nodes

46 4 +/- 2 A decrease in the proximity between FITC sites within the N-domain and a 9 +/- 3 A increase

47 Both FITC-TrapG and NIR-TrapG specifically imaged subcutaneou

48 In vitro binding of both FITC-TNYL-RAW and (64)Cu-DOTA-TNYL-RAW to cancer cells w

49 In vitro, both FITC-TNYL-RAW and (64)Cu-DOTA-TNYL-RAW were selectively

50 ortical neurons with the ER agonists E-6-BSA-FITC [beta-estradiol-6-(O-carboxymethyl)oxime-bovine ser

51 rticles, (AuNP@Cit/Cytc-FITC or AuNP@Cit/BSA-FITC), low limits of detection for Cyt c (LOD = 370 pM)

52 Using E2-BSA-FITC (fluorescein isothiocyanate) macromolecular complex

53 All E2-BSA-FITC binding neurons expressed L-type calcium channels.

54 s, revealed rapid Ca(2+) responses in E2-BSA-FITC binding neurons within minutes that culminated in a

55 nal markers labeled subpopulations of E2-BSA-FITC binding neurons.

56 ane of soma and neuronal processes in E2-BSA-FITC binding neurons.

57 agonist, DPN, partially competed for E2-BSA-FITC binding.

58 The same neurons in which E2-BSA-FITC induced a [Ca(2+)]i rise also exhibited activated p

59 jugated with fluorescein isothiocyanate (BSA-FITC) model proteins on hydrophilic silicon substrates w

60 No membrane binding was observed with BSA-FITC.

61 Migration toward DLN was evaluated by FITC skin painting, transgenic GFP skin tissue grafting,

62 Apoptosis, measured by FITC-annexin, occurs maximally in the second to third we

63 pases and caspase-3 were detected in situ by FITC-VAD-fmk staining and caspase-3 substrate, respectiv

64 ing capacity on the mitochondrial surface by FITC-labeled tBid(G94E) also confirmed that tBid binding

65 Conversely, FITC-labeled blastema cells were restricted to distal CT

66 CAR-T cells (specific for the corresponding FITC or PNE) to Her2-expressing tumor cells, and afford

67 of multi-shell nanoparticles, (AuNP@Cit/Cytc-FITC or AuNP@Cit/BSA-FITC), low limits of detection for

68 e contact sensitizer dibutyl phthalate (DBP)-FITC.

69 Both Nb and DBP-FITC induced extensive transcriptional changes that invo

70 tified no shared pathways between Nb and DBP-FITC, but revealed a type-I IFN (IFN-I) signature unique

71 the induction of Th2 immune responses by DBP-FITC.

72 In DBP-FITC-treated mice, TN DC upregulated expression of CD86

73 In contrast, the response to DBP-FITC was not affected by IFN-I receptor blockade, a find

74 ne (NAC) reduced ROS formation and decreased FITC-dextran leakage in Hcy treated HRECs.

75 ealed that CyLiPns could effectively deliver FITC-siRNA up to 360mum skin depth.

76 rum levels of lipopolysaccharide and dextran-FITC in mice with CDI that were exposed to PPI.

77 rum levels of lipopolysaccharide and dextran-FITC were measured to reflect the barrier permeability o

78 0-kDa dextran-Texas red, and 500-kDa dextran-FITC.

79 4 hours after AC injection of 40-kDa dextran-FITC.

80 model) using a newly developed 3-dimensional FITC-Imaris technique.

81 ently conjugated to common fluorescent dyes (FITC, Alexa647 and BODIPy-TR), mixed with pluronic F68 a

82 -induced change in FITC fluorescence enabled FITC/BSA-AuNCs to detect an ammonia product-related enzy

83 orescence quenching of AuNCs by H2O2 enabled FITC/BSA-AuNCs to ratiometrically detect the H2O2 produc

84 g protein completely eliminated SNP-enhanced FITC-insulin uptake.

85 Under single wavelength excitation, FITC/BSA-stabilized AuNCs (FITC/BSA-AuNCs) emitted fluor

86 arized 488 nm laser pulsed at 137 Hz excited FITC-glucagon.

87 aracellular permeability and size exclusion, FITC-labeled dextran ranging in size from 10 to 70 kDa w

88 ells for PEG-like molecules (CH3-PEG5K-FITC (FITC = fluorescein isothiocyanate) and eight-arm PEG20K-

89 A green emitting fluorophore, FITC (fluorescein isothiocyanate), whose luminescence is

90 tly dependent on the presence of both folate-FITC and FR-positive cells and was dose titratable with

91 ing the specificity of redirection by folate-FITC.

92 low folate-FITC uptake, areas of high folate-FITC uptake within human atherosclerotic plaques had an

93 Hot spots showed significantly higher folate-FITC uptake than cold spots (P < 0.001).

94 ugated to fluorescein isothiocyanate (folate-FITC) can redirect and regulate FITC-specific CAR-T cell

95 Compared with areas with low folate-FITC uptake, areas of high folate-FITC uptake within hum

96 ed to determine the exact location of folate-FITC uptake.

97 n from 20 patients and incubated with folate-FITC for 30 min.

98 ve cells and was dose titratable with folate-FITC switch.

99 sion was increased by approximately 70-fold (FITC-lectin binding), tumor vascular permeability was en

100 production, and serum IgE levels, following FITC sensitization and challenge.

101 itic cells in draining lymph nodes following FITC sensitization.

102 f injured explants were 6%, 40%, and 32% for FITC, TRITC, and TAMRA, respectively, compared to uninju

103 ITC -p b-sCD44 was 17.4% (P < 0.001) and for FITC b-sCD44 was 11.7% (P < 0.001) compared with b-album

104 rface adsorption of solute was strongest for FITC and weakest for TAMRA; no solutes negatively affect

105 Although we found FITC-labeled LPS in DLN within minutes of injection, dra

106 lymers were successfully immunoisolated from FITC-mouse antibody and pro-inflammatory cytokines.

107 orescein and "eat-me" phagocytic signals (Gd-FITC-LiLa) a) demonstrates high relaxivity that improves

108 The AuNP-GSH-FITC fluorescent probe was firstly developed and used fo

109 Using the AuNP-GSH-FITC probe, a droplet-based microfluidic fluorescent sen

110 athione-fluorescein isothiocyanate (AuNP-GSH-FITC) probe coupled with on-line droplet-based microflui

111 ntact hypersensitivity induced by the hapten FITC in combination with the sensitizing agent dibutyl p

112 the epicutaneous application of the haptens FITC and oxazolone confirmed that topically applied cFLI

113 o afford F-UiO NMOFs with exceptionally high FITC loadings, efficient fluorescence, and excellent rat

114 (TRITC), fluorescein isothiocyanate isomer I(FITC) and DNA molecules, forming neutral LDH-nanosheet c

115 Retinopathy was qualitatively assessed in FITC-dextran-perfused retinas, and preretinal NV was qua

116 The pH-induced change in FITC fluorescence enabled FITC/BSA-AuNCs to detect an am

117 d to a loss of EBF with TPN (60% increase in FITC-dextran permeability, 40% decline in transepithelia

118 concanamycin A-sensitive proton transport in FITC-loaded lysosomes.

119 Increased FITC-dextran leakage was observed from pre-existing vess

120 tight junction protein expression, increased FITC dextran leakage, decreased transcellular electrical

121 yers, 3h OGD and 24h reoxygenation increased FITC-dextran leakage, indicating disruption of intercell

122 y after photobleaching (MP-FRAP) of injected FITC-BSA, a 32.6% decrease in lymph speed was observed i

123 r erythrocyte flow and reduction of injected FITC-inulin were developed, each validated using the nep

124 ate-labeled, gluconic acid-modified insulin (FITC-G-Ins) proteins were immobilized on the exterior su

125 l permeability, as revealed by intratracheal FITC-dextran tracking, serum Club Cell protein 16 measur

126 rhodamine-lactam and fluorescein isocyanate (FITC) leads to efficient metabolic incorporation of FITC

127 Green-emitting fluorescein-5-isothiocyanate (FITC) was conjugated to the amino groups of bovine serum

128 Lys(514) with fluorescein 5-isothiocyanate (FITC), which physically blocks access to the nucleotide

129 tumumab and fluorescein 5(6)-isothiocyanate (FITC) panitumumab.

130 conjugated with fluorescein isothiocyanate (FITC) and DOTA.

131 was tagged with fluorescein isothiocyanate (FITC) and made into nanoparticles (135 +/- 3 nm diameter

132 he high affinity fluorescein isothiocyanate (FITC) containing peptide, FITC-NH-(CH2)4-CO-pY-Q-G-L-S-a

133 t-treatment with Fluorescein Isothiocyanate (FITC) labeled 8-OHdG antibody.

134 imaging a 20 muM fluorescein isothiocyanate (FITC) labelling solution on mammalian tissue.

135 bes labeled with fluorescein isothiocyanate (FITC) or digoxigenin (Dig), followed by dual enzymatic l

136 Fluorescein isothiocyanate (FITC) was conjugated to a mouse monoclonal antibody, Fc1

137 Fluorescein isothiocyanate (FITC) was covalently conjugated to a UiO NMOF to afford

138 ely labeled with fluorescein isothiocyanate (FITC), a probe that specifically reacts with Lys-515 in

139 ed fluorophores (fluorescein isothiocyanate (FITC), tetramethylrhodamine isothiocyanate (TRITC), and

140 contrast agent, fluorescein isothiocyanate (FITC), we aimed to explore the potential role of FR-beta

141 bited binding of fluorescein isothiocyanate (FITC)-AS1411 to plasma membrane nucleolin 56 +/- 10% SE

142 of Man-SNPs with fluorescein isothiocyanate (FITC)-concanavalin A (Con A) was determined using a fluo

143 permeability to fluorescein isothiocyanate (FITC)-conjugated dextran, and (ii) AJC structure using i

144 Specially, fluorescein isothiocyanate (FITC)-conjugated lectin from Lens culinaris (lentil) (FI

145 demonstrated by fluorescein isothiocyanate (FITC)-dextran translocation to the circulation.

146 travenously with fluorescein isothiocyanate (FITC)-dextran.

147 se-2/9 activity, fluorescein isothiocyanate (FITC)-gelatin.

148 e, and increased fluorescein isothiocyanate (FITC)-inulin diffusion across the polarized cell monolay

149 microengines and fluorescein isothiocyanate (FITC)-labeled avidin (Av-FITC) as the template.

150 Fluorescein isothiocyanate (FITC)-labeled control siRNA delivered intranasally was f

151 The flux of fluorescein isothiocyanate (FITC)-labeled dextran across monolayers or the mouse epi

152 labeled insulin, fluorescein isothiocyanate (FITC)-labeled IAPP, anti-insulin, and anti-IAPP antibodi

153 ed, EC uptake of fluorescein isothiocyanate (FITC)-labeled insulin.

154 is, diffusion of fluorescein isothiocyanate (FITC)-labeled markers, and immunostaining for tight junc

155 A fluorescein isothiocyanate (FITC)-labeled peptide derived from the ATR cofactor, ATR

156 oefficients D of fluorescein isothiocyanate (FITC)-pepsin were measured in rennet gels across a range

157 or SPION-Ran] or fluorescein isothiocyanate (FITC)-sODN-mmp9 or FITC-sODN-Ran; we then delivered thes

158 incubation with fluorescein isothiocyanate (FITC)-tagged anti-human IgG.

159 derivatised with fluorescein isothiocyanate (FITC).

160 s a quencher for fluorescein isothiocyanate (FITC).

161 ange [containing fluorescein isothiocyanate (FITC)], by utilizing a difluoromethylphenol-glucuronide

162 (2) = 0.964) and fluorescein isothiocyanate (FITC, R(2) = 0.973).

163 AHENTA with fluorescein-5-yl isothiocyanate (FITC) gave fluorescent probes that bound at nanomolar co

164 s (e.g., -COCH3, fluorescein isothiocyanate; FITC).

165 rgeting sequence peptide (F-PTS1, acetyl-C{K(FITC)}GGAKL) for investigating pH regulation of glycosom

166 sessed using both albumin-Alexa568 and 69-kD FITC-dextran; however, diabetic animals demonstrated sig

167 a intravital microscopic analysis of 150 kDa FITC-dextran-perfused blood vessels within discrete woun

168 the ability to exclude 500 kDa and 2000 kDa FITC-dextran molecules and the maintenance of the cell b

169 sm to determine the binding of ConA to 4 kDa FITC-dextran by measuring the change in the rotational c

170 of this ligand, the ranges of ConA and 4 kDa FITC-dextran concentrations capable of being explored we

171 vere, allowing the entry of 3 kDa and 40 kDa FITC-dextrans, but the membrane was not completely broke

172 NaF and 40-kDa FITC-D reached higher peak concentrations and were clear

173 mL sodium fluorescein (NaF), 25 mg/mL 40-kDa FITC-D, or 25 mg/mL 70-kDa FITC-D, with (n = 9) or witho

174 Average 40- and 70-kDa FITC-D concentrations in the retina/choroid peaked at 54

175 on, and 48 and 72 hours after 40- and 70-kDa FITC-D injections, respectively.

176 , 25 mg/mL 40-kDa FITC-D, or 25 mg/mL 70-kDa FITC-D, with (n = 9) or without (n = 9) immediate euthan

177 ed from the eye more rapidly than was 70-kDa FITC-D.

178 ed by fluorescein-tagged annexin-V labeling (FITC-annexin-V), as well as by terminal nucleotide nick-

179 rly demonstrated using green and red labels (FITC, DyLight 488, Alexa 568, and Alexa 596).

180 lication the appearance of hapten-laden LCs (FITC+, CD11c+, Langerin+) in the lymph nodes of PAF rece

181 jugated lectin from Lens culinaris (lentil) (FITC-lectin) was tested on the different buffer conditio

182 he cellular uptake properties of cAMP-loaded FITC-BA-MSN with and without G-Ins capping were investig

183 paracellular permeability to macromolecular FITC-dextran.

184 structure, 20 nm fluorescent nanoparticles, FITC-BSA, and Alexa Fluor(R) 488 conjugated siRNA were e

185 .4-, and 2.9-fold greater for nanoparticles, FITC-BSA, and Alexa-siRNA, respectively, when compared t

186 res, POPOP (lambda(max, emission) = 428 nm), FITC (517 nm), S101 (600 nm), Zn PhCy (710 nm), and IR 7

187 permeability, assayed by the accumulation of FITC-dextran in plasma.

188 ulate the solvent-accessible surface area of FITC and FMP bound to SERCA crystal structures, revealin

189 alitatively related to diffusion behavior of FITC-pepsin in these dairy gels.

190 Binding of FITC-TNYL-RAW and (64)Cu-DOTA-TNYL-RAW to CT26 and PC-3M

191 Examination of DC capture of FITC from painted skin, DC isolation from skin explant c

192 e experimental results for the collection of FITC-labeled bovine serum albumin (BSA, 0.033nM) were as

193 ouble-release system is that the decrease of FITC-G-Ins release with cycles can be balanced by the re

194 in KO mice indicated more the development of FITC sensitization than an irritative reaction.

195 sity of the ML and PCL from the diffusion of FITC-dextran dissolved in the ASL of unperturbed, well-d

196 ich is regulated by the gatekeeper effect of FITC-G-Ins.

197 eads to efficient metabolic incorporation of FITC and rhodamine-lactam into bacterial peptidoglycan.

198 cules through site-specific incorporation of FITC or grafting of a peptide neo-epitope (PNE) into the

199 LB/c mice received subcutaneous injection of FITC-conjugated dextran (DX) probes into the ear skin an

200 he free-space emission and SPCF intensity of FITC on 20 nm nickel thin film were also measured to dem

201 ements confirmed the specific interaction of FITC-tagged TMPMs with their respective TMH.

202 ay to monitor binding and internalization of FITC labeled POS by ARPE-19, human fetal RPE (hfRPE), an

203 by measuring apical-basolateral movements of FITC-dextran, respectively.

204 st, JNJ 7777120, contained a lower number of FITC-positive dendritic cells.

205 Large numbers of FITC(+) epidermal cells became detectable 12-24 hours af

206 F-actin staining with phalloidin, passage of FITC-conjugated dextran through a monolayer of lung epit

207 as assessed after 14 days after perfusion of FITC-dextran.

208 Transcardial perfusion of FITC-labeled albumin suggested that local ischemia was a

209 t by confirming dose-dependent permeation of FITC-insulin and sulforhodamine-B.

210 rular filtration, as assessed by the rate of FITC-inulin clearance from the blood, which, in turn, wa

211 The recognition of FITC-APBA to sialylated TRITC-AF leads to the FRET signa

212 these models, as shown by the reductions of FITC-dextran gut translocation, serum interleukin-6 (IL-

213 increased uptake and decreased secretion of FITC-labeled Albumin.

214 The selectivity of FITC-G-Ins release toward a series of carbohydrate trigg

215 ionally, a concentration-dependent uptake of FITC labeled Bla g 2 by fibrocytes was observed, but was

216 trate macropinocytosis through the uptake of FITC-dextran and amiloride inhibition of Francisella LVS

217 antibody Erbitux enabled selective uptake of FITC-labeled Ki-67 antibody TuBB-9 in EGFR-positive cell

218 pse images were taken of labeled TM cells on FITC-collagen.

219 myocyte diameter and length were measured on FITC-wheat germ agglutinin-stained sections.

220 extramers and with PE-, allophycocyanin-, or FITC-based reagents.

221 uorescein isothiocyanate (FITC)-sODN-mmp9 or FITC-sODN-Ran; we then delivered these probes by intrace

222 igned to contain a donor/acceptor FRET pair (FITC and DABCYL).

223 droplets containing size-selected particles, FITC-albumin, or Lsr-F were recovered, re-electrosprayed

224 rescein isothiocyanate) and eight-arm PEG20K-FITC) was at least 10-80-fold greater than that of 293T

225 type cells for PEG-like molecules (CH3-PEG5K-FITC (FITC = fluorescein isothiocyanate) and eight-arm P

226 -PEG5K-NH2) and PEG-like molecule (CH3-PEG5K-FITC, CH3-PEG5K-SHPP, and CH3-PEG5K-NIR797) was14-137 ng

227 in isothiocyanate (FITC) containing peptide, FITC-NH-(CH2)4-CO-pY-Q-G-L-S-amide (8; Kd = 0.35 microM)

228 phosphatidylserine and binds prothrombinase (FITC Xa.factor Va).

229 Punctate FITC signal was observed on plasma membrane of soma and

230 nate (folate-FITC) can redirect and regulate FITC-specific CAR-T cell activity toward folate receptor

231 s, but only when pretargeted with a relevant FITC-labelled antitumour antibody.

232 Several FITC-tagged TMPMs specifically bound to Cdr1p and blocke

233 rin(+) epidermal cells exhibited significant FITC signals.

234 tic and fluorescent core/shell of Fe3O4@SiO2(FITC) was tested for their ability to deliver Notch-1 sh

235 as Notch-1 shRNA in this report, Fe3O4@SiO2(FITC)/PEI-FA can be exploited as a novel, non-viral, and

236 agnetic targeting capabilities of Fe3O4@SiO2(FITC)/PEI-FA, our results show that by complexing with a

237 ignificant preferential uptake of Fe3O4@SiO2(FITC)/PEI-FA/Notch-1 shRNA nanocomplex by MDA-MB-231 cel

238 Our results showed that Fe3O4@SiO2(FITC)/PEI-FA/Notch-1 shRNA nanoparticles are 64 nm in di

239 udies, and the nuclear localization of ssDNA-FITC suggest that nano-LDHs have potential application a

240 ive AuNCs were used as an internal standard, FITC/BSA-AuNCs offered a sensitive and reversible ratiom

241 In fate-mapping studies, FITC-labeled vertebra periosteal cells were detected in

242 We used enzyme reverse mode to synthesize FITC monophosphate (FMP) on SERCA, producing a phosphory

243 and glycolic acid residue and an N-terminal FITC fluorophore appended via a thiourea linkage.

244 jugate showed capture efficiency better than FITC-G6-COOH-5aSlex conjugate.

245 ation-specific proteolysis demonstrated that FITC labeling does not induce closure of the cytoplasmic

246 The FITC-dextrans (4 and 20 kDa) were able to migrate in the

247 e second irradiation at 490 nm activated the FITC-labeled TuBB-9, which caused inactivation of the Ki

248 with a static adhesion assay ex vivo and the FITC-lectin perfusion method in vivo.

249 At a higher dose (120 nmol/kg), the FITC-sODN-mmp9 probe revealed significant knockdown of M

250 ross-links and instantaneously liberates the FITC-BSA under 2 cm thick tissue.

251 t photomultiplier tubes for detection of the FITC and Cy5 signal.

252 that internalized POS, the brightness of the FITC signal from the cells, and the surface density of t

253 Most (>90%) of the FITC(+) epidermal cells expressed Langerin, and >95% of

254 -yl (NBD) and N-fluorescein-5-thiocarbamoyl (FITC) labels, respectively.

255 This FITC is conjugated in end-terminal of activatable fluoro

256 This FITC-conjugated BSA acted as a template for the synthesi

257 is study when purified aggrecan was added to FITC-conjugated hyaluronan, no internalization of hyalur

258 The purified TAT-SOD was conjugated to FITC-MSN forming FMSN-TAT-SOD.

259 % for injured and sliced explants exposed to FITC).

260 he draining lymph node following exposure to FITC and in reduced expression of CCR7 and MMP-9 in sple

261 ro HCECs were subjected to immunostaining to FITC-phalloidin and antibodies to different junction com

262 to a significant increase in permeability to FITC dextran.

263 further assessed in terms of permeability to FITC dextran.

264 NO production, and elevating permeability to FITC-dextran 70 in monolayers of cells expressing wild-t

265 PAF failed to increase permeability to FITC-dextran 70 in monolayers of cells transfected with

266 ased paracellular intestinal permeability to FITC-dextran.

267 ier in vivo by percutaneous sensitization to FITC in TGM3/KO (n=64) and C57BL/6 wild-type (WT) mice (

268 arrier function and higher susceptibility to FITC sensitization indicating that TGM3 has a significan

269 As in vivo tracer, FITC penetration from skin surface followed by two-photo

270 Using FITC dextran conjugates, we demonstrate that sea urchin

271 ne exclusively expressing Nox1 (HT-29) using FITC-labeled NoxA1ds.

272 Leukostasis was assessed using FITC-conjugated ConA to label leukocytes.

273 microscopy experiments were conducted using FITC-labeled 5 and confirmed binding of 5 to WM-115 mela

274 s were measured on choroidal flatmount using FITC-dextran.

275 entary distance measurements were made using FITC or 5-iodoacetamidofluorescein (IAF) bound to Cys(67

276 luorescence polarization assay that utilized FITC-labeled peptide ligands.

277 r cell line, as evidenced from the annexin V-FITC/PI assay.

278 Cell cycle analysis and Annexin V-FITC/PI binding assay showed that combination of HA and

279 Annexin V-FITC/PI staining assays confirm that the cell death indu

280 ed by WST-1 cytotoxicity assay and annexin V-FITC/propidium iodide (PI) staining as apoptosis-necrosi

281 for PET imaging, and a fluorescent version, FITC-PEG4-cRGD2, for in vitro work).

282 characterize FMP-SERCA (ATP.E2 state) versus FITC-SERCA in Ca(2+)-free, Ca(2+)-bound, and actively cy

283 e, beginning 1 hour after injection, whereas FITC-D-injected eyes did not show elevated retina/choroi

284 With FITC as the reference signal, the mono- and dual-color e

285 ific H(4)R antagonists before challenge with FITC led to a significant reduction in ear edema, inflam

286 sured by perfusing the anterior chamber with FITC-labeled dextran for 30 minutes at a fixed IOP of ap

287 ional animals, perfluorocarbon combined with FITC (fluorescein isothiocyanate) was administered for p

288 decreased probe accessibility compared with FITC-SERCA, indicating that ATP exhibits enhanced dynami

289 The assay involves derivatization with FITC followed by CE-LIF using 0.5 mM hydroxyl propyl-bet

290 Mice were anaesthetized, gavaged with FITC-dextran for measures of gastrointestinal permeabili

291 mary detection reagents were identified with FITC-labeled probes and analyzed by fluorescence microsc

292 P < 0.01) compared with cells incubated with FITC-AS1411 only.

293 ragments are site-specifically modified with FITC using genetically encoded noncanonical amino acids.

294 as Fu(live), the animals were perfused with FITC-dextran and Fu determined.

295 is in mice was assessed after perfusion with FITC-conjugated concanavalin A.

296 y in vitro cultures were fixed, stained with FITC-phalloidin and hair cells were counted.

297 P-biotin conjugate followed by staining with FITC-avidin.

298 n neuroblastoma (SK-N-SH) cells treated with FITC conjugated Abeta1-40 localized Abeta to the nucleus

299 microvascular networks were visualized with FITC conjugated BSI-lectin labeling and arteriole diamet

300 proteolysis, measured by gelatin zymography, FITC-gelatin conversion, and DQ-gelatin degradation assa