ライフサイエンスコーパス: carboxyfluorescein

1 cohol) layer contains the self-quenching dye carboxyfluorescein.

2 g cells with Oregon Green and two isomers of carboxyfluorescein.

3 ose formed by Cx43 in terms of permeation to carboxyfluorescein.

4 These heterotypic channels were permeable to carboxyfluorescein.

5 py using 2',7'-bis(2-carboxyethyl)-5-(and -6)carboxyfluorescein.

6 RhB in intralipid and to measure pH using 6-carboxyfluorescein.

7 d rabbit sclera to water, dexamethasone, and carboxyfluorescein.

8 us, monitored by the simultaneous release of carboxyfluorescein.

9 sensitive dye 2',7'-bis(2-carboxyethyl)-5(6)-carboxyfluorescein.

10 ow fluorimetry in SM vesicles with entrapped carboxyfluorescein.

11 asured by leakage of the encapsulated marker carboxyfluorescein.

12 ocated anion conductive channel permeable to carboxyfluorescein.

13 fluorescent dye 2'7'-bis(carboxyethyl)5-(6)-carboxyfluorescein.

14 emain relatively unaltered from the parent 3-carboxyfluorescein.

15 ovement in cellular brightness compared to 3-carboxyfluorescein.

16 TP filter was used to enhance detection of 6-carboxyfluorescein 4-fold over fluorescein, even though

17 The leakage rate of trapped 5, 6-carboxyfluorescein (5(6)CF) and the proton permeability

18 optimal conditions for two model analytes, 5-carboxyfluorescein (5-FAM) and sodium fluorescein (FL),

19 organ culture systems was developed using 6-carboxyfluorescein, 5-carboxyfluorescein, and fluorescei

20 on coefficient of four different dyes, 5-(6)-carboxyfluorescein, 5-chloromethylfluorescein, Oregon gr

21 epatocytes into its fluorescent derivative 6-carboxyfluorescein (6-CF) and secreted into the canalicu

22 s axon in the living leech was filled with 6-carboxyfluorescein (6-CF) dye and cut with an argon lase

23 The assay uses highly specific 6-carboxyfluorescein (6-FAM) and biotin labeled antisense

24 Guanines of G-quadruplex TBA-conjugated carboxyfluorescein (6-FAM) bound with thrombin do not re

25 ng guanine (G)-rich DNA aptamer-conjugated 6-carboxyfluorescein (6-FAM) capable of rapidly capturing

26 laying optimal performance was composed of 6-carboxyfluorescein (6-FAM) on the peptide N-terminus, an

27 Similar results were obtained with 5-(and-6)-carboxyfluorescein-6-aminohexyl ouabain as acceptor.

28 azol-4-yl]-6-aminohexyl ouabain or 5-(and-6)-carboxyfluorescein-6-aminohexyl ouabain bound to the res

29 ing donor/acceptor pairs were synthesized: 6-carboxyfluorescein/6-carboxy-X-rhodamine (FAM-ROX), 3-(e

30 e oligonucleotides with a 5' reporter dye (6-carboxyfluorescein), a quencher dye (6-carboxy-tetrameth

31 ased on the inhibition of the transport of 6-carboxyfluorescein, a high-affinity hOAT1 substrate (Km

32 rnal volume of each vesicle, we encapsulated carboxyfluorescein, a pH-sensitive dye whose fluorescenc

33 asured with 2',7'-bis(carboxyethyl)-S-(and 6)carboxyfluorescein acetoxy methylester/fluorometry.

34 oaded with BCECF (2',7'-bis(2-carboxyl)-5(6)-carboxyfluorescein-acetoxyethyl ester).

35 probe, 2',7'-bis-(2-carboxyethyl)-5-(and-6)-carboxyfluorescein acetoxymethyl ester (BCECF-AM), that

36 orescent probe 2',7'-bis(2-carboxyethyl)-5,6-carboxyfluorescein-acetoxymethyl ester was used to quant

37 dicator 2',7'-bis-(2-carboxyethyl)-5-(and-6)-carboxyfluorescein-acetoxymethyl ester, the initial rate

38 nd loaded with 2',7'-bis(2-carboxyethyl)-5(6)carboxyfluorescein-acetoxymethyl ester.

39 the small solute 2',7'-bis-2-carboxyethyl-5-carboxyfluorescein-acetoxymethyl-ester (BCECF).

40 ransport large hydrophilic molecules such as carboxyfluorescein across lipid bilayers.

41 Confocal analysis with carboxyfluorescein-alendronate confirmed the microcalcif

42 cumber (Cucumis sativus L.) was mapped using carboxyfluorescein and (14) C as mobile tracers.

43 AT-selective fluorescent tracer substrates 5-carboxyfluorescein and 6-carboxyfluorescein were used.

44 sensing was demonstrated using mixtures of 6-carboxyfluorescein and [Ru 2,2'-(bipyridyl)3]2+ as a pH

45 Passive fluorescent markers such as carboxyfluorescein and a 10-kDa dextran polymer crossed

46 citation ratio of 2,7-bis(carboxyethyl)-5(6)-carboxyfluorescein and calibrated with nigericin and ele

47 measured using 2',7'-bis-(2-carboxyethyl)-5-carboxyfluorescein and compared to that observed with ex

48 -thrombin binding aptamer was labeled with 6-carboxyfluorescein and exploited as a selective fluoresc

49 ased sensing was demonstrated for pH using 6-carboxyfluorescein and for protein affinity or immunoass

50 th the pH probe 2',7'-bis(carboxyethyl)-5(6)-carboxyfluorescein and mounted in a bilateral perfusion

51 show enhanced water solubility compared to 3-carboxyfluorescein and persist in an open, visible light

52 nd Halobacterium salinarum, retain entrapped carboxyfluorescein and resist aggregation in the whole r

53 was developed using 6-carboxyfluorescein, 5-carboxyfluorescein, and fluorescein.

54 tive indicator 2',7'-bis(carboxyethyl)-5-(6)-carboxyfluorescein, and Na+ transport was measured under

55 idin-modified labels-horseradish peroxidase, carboxyfluorescein, and photon-upconversion nanoparticle

56 ty of the complex of wild-type RNase A and 6-carboxyfluorescein approximately d(AUAA) at varying pHs

57 ecreases the stability of the complex with 6-carboxyfluorescein approximately d(AUAA) by 2.3 kcal/mol

58 determined with the fluorogenic substrate: 6-carboxyfluorescein approximately dArXdAdA approximately

59 ke were correlated with molecular size: 5(6)-carboxyfluorescein (approximately 32%), 7-hydroxycoumari

60 hesized by their click reaction with propyne carboxyfluorescein are seen to accumulate around the nuc

61 ntaining calcium, adenosine triphosphate, or carboxyfluorescein are tethered to plasmon-resonant holl

62 iggered the release of liposome-encapsulated carboxyfluorescein at both neutral and acidic pH.

63 e presence and absence of pH-sensitive dyes (carboxyfluorescein at pH 6.5, phenol red at pH 7.5, and

64 these substrates, we developed an improved 5-carboxyfluorescein-based FRET substrate, which is better

65 nown hOAT1 substrates determined using the 6-carboxyfluorescein-based inhibition assay correlated wel

66 orescent probes, 2',7'-bis(carboxyethyl)-5,6-carboxyfluorescein (BCECF) and fura-2, respectively.

67 using 2',7'-bis-(2-carboxyethyl)-5-(and -6)-carboxyfluorescein (BCECF) as a cytoplasmic pH indicator

68 (estimated by 2',7'-bis(2-carboxyethyl)-5(6)-carboxyfluorescein (BCECF) fluorescence).

69 (2)/HCO(3)(-) by 2',7'-bis(carboxyethyl)-5,6-carboxyfluorescein (BCECF) fluorometry of stably slc4a10

70 itive dye 2',7'-bis-(carboxyethyl)-5-(and-6)-carboxyfluorescein (BCECF) indicated that previous K(m)

71 or dye 2', 7'-bis-(2-carboxyethyl)-5-(and -6)carboxyfluorescein (BCECF) is routinely used to measure

72 minal aorta, using 2',7'-biscarboxyethyl-5(6)carboxyfluorescein (BCECF) on a microscope-based fluorim

73 tio imaging with 2',7'-bis(carboxyethyl)-5,6-carboxyfluorescein (BCECF) or sodium-binding benzofuran

74 ve fluoroprobe 2'7'-bis(2-carboxyethyl)-5(6)-carboxyfluorescein (BCECF) or the sodium-binding benzofu

75 fluorescent dye 2',7'-bis(carboxyethyl)-5,6-carboxyfluorescein (BCECF) to study the regulation of in

76 cein derivative 2,7-bis(2-carboxyethyl)-5(6)-carboxyfluorescein (BCECF) was monitored by high-through

77 nt dyes fura-2 and 2',7'-bis(carboxyethyl)-5-carboxyfluorescein (BCECF) were used to measure [Ca2+]i

78 ated by 2',7'-Bis-(2-Carboxyethyl)-5-(and-6)-carboxyfluorescein (BCECF), a pH sensitive fluorescent d

79 thyl of 2',7'-bis-(2-carboxyethyl)-5-(and 6)-carboxyfluorescein (BCECF), BCECF conjugated to 70-kDa d

80 essed by 2',7'-bis(2-carboxyethyl)-5-(and-6)-carboxyfluorescein (BCECF), Fura-2 and differential inte

81 ium performed with 2',7-biscarboxyethyl-5(6)-carboxyfluorescein (BCECF), the selective V-ATPase inhib

82 c monitoring of 2',7'-bis(carboxyethyl)-5, 6-carboxyfluorescein (BCECF), to assess changes in pHi or

83 ive dye, 2',7'-bis(2-carboxyethyl)-5-(and-6)-carboxyfluorescein (BCECF), were coated onto the probe s

84 used is 2',7'-bis-(2-carboxyethyl)-5-(and-6)-carboxyfluorescein (BCECF), whose lifetime tau (pH 4.5,

85 y with 1',7'- bis-(2-carboxyethyl)-5-(and-6)-carboxyfluorescein (BCECF)-dextran demonstrated that gra

86 surements with 2',7'-bis-(carboxyethyl)-5(6)-carboxyfluorescein (BCECF).

87 ent dye 2',7'-bis-(2-carboxyethyl)-5-(and-6)-carboxyfluorescein (BCECF).

88 ent dye 2',7'-bis-(2-carboxyethyl)-5-(and-6)-carboxyfluorescein (BCECF).

89 sensitive dye 2', 7'-bis-(carboxyethyl)-5(6)-carboxyfluorescein (BCECF).

90 uorescent dye 2',7'-bis(2-carboxyethyl)-5(6)-carboxyfluorescein (BCECF).

91 fluorochrome, 2',7'-bis(carboxyethyl)-5-(6)-carboxyfluorescein (BCECF).

92 fluoroprobe 2', 7'-bis(2-carboxyethyl)-5(6)-carboxyfluorescein (BCECF).

93 luorescent probe 2',7'-bis(carboxyethyl)-5,6-carboxyfluorescein (BCECF).

94 n conjugate of 2'7'-bis(2-carboxyethyl)-5(6)-carboxyfluorescein (BCECF-dextran).

95 (pyranin or [2',7'-bis (2-carboxyethyl)-5(6)-carboxyfluorescein] [BCECF]) was trapped in egg phosphat

96 tive membrane permeability, releasing 376-Da carboxyfluorescein but not 4-kDa fluorescein isothiocyan

97 5' labeled with fluorescent probes such as 6-carboxyfluorescein can be rapidly separated and quantifi

98 er glutamate treatment was determined with a carboxyfluorescein caspase-3 detection kit.

99 Transformation of the carboxyfluorescein (CCFSE)-labeled epithelial seam is de

100 CPe liposomes release encapsulated anionic carboxyfluorescein (CF) 20 times faster than PC liposome

101 We assessed heat cycle-triggered release of carboxyfluorescein (CF) and doxorubicin (DXR) from TSLs.

102 labeled with N-hydroxysuccinimidyl esters of carboxyfluorescein (CF) and rhodamine (Rho) to enable me

103 asuring the efflux into the superfusate of 5-carboxyfluorescein (CF) applied to the stroma of deepith

104 uring the early stages of tuberization using carboxyfluorescein (CF) as a phloem-mobile tracer, and t

105 ], were compared in their ability to release carboxyfluorescein (CF) from 100-nm large unilamellar ve

106 ng of the fluorescent polyanionic probe 5(6)-carboxyfluorescein (CF) to various generations of dendri

107 course of transbilayer AOFA flip-flop using carboxyfluorescein (CF) trapped within the lipid vesicle

108 oteins spectrin and protein 4.1 labeled with carboxyfluorescein (CF), at two different compositions o

109 e unilamellar vesicles (LUVs) preloaded with carboxyfluorescein (CF).

110 es by monitoring self-quenching of entrapped carboxyfluorescein (CF).

111 Carboxyfluorescein (CFL) was used as a fluorescent dye w

112 d by flow cytometric analysis for binding of carboxyfluorescein conjugated VAD-fmk peptide to activat

113 n by utilizing a pH sensitive dye, 5-(and-6)-carboxyfluorescein, conjugated to free lysine residues o

114 erized, each containing a fluorescent dye (6-carboxyfluorescein) connected to the 5' end via a photoc

115 indicator 2,7-bis-(2-carboxyethyl)-5-(and-6)-carboxyfluorescein corroborated these changes in pH(cyto

116 e phenomenon that high-density deposition of carboxyfluorescein covalently coupled to silica microsph

117 ancomycin from Streptomyces orientalis and 5-carboxyfluorescein-D-Ala-D-Ala-D-Ala (5-FAM-(DA)(3)) is

118 a 4-(4-dimethylaminophenylazo)benzoyl and 5-carboxyfluorescein (Dabcyl/Fam) pair and are based on kn

119 The calibration curves for fluorescein and 5-carboxyfluorescein demonstrated good linearity in the co

120 Fluorescence intensity of the pH-sensitive carboxyfluorescein derivative 2,7-bis(2-carboxyethyl)-5(

121 ion of the pH-sensitive dye bis-carboxyethyl carboxyfluorescein dextran, show oscillating pH changes

122 The cells were also labeled with 6-carboxyfluorescein diacetate (6-CFDA) as an internal sta

123 copy to quantify the transport kinetics of 6-carboxyfluorescein diacetate (6-CFDA), which is processe

124 This time-dependent decrease in carboxyfluorescein diacetate (CFDA) fluorescence was the

125 The fluorescent probes, carboxyfluorescein diacetate (CFDA) for cytoplasmic este

126 nication, we loaded the fluorescent tracer 5-carboxyfluorescein diacetate into the cytoplasm, and qua

127 zyme-linked immunosorbent spot (ELISpot) and carboxyfluorescein diacetate succinimide ester (CFSE) pr

128 Injection of carboxyfluorescein diacetate succinimide ester-labeled C

129 inal binding dye molecules such as 5-(and-6)-carboxyfluorescein diacetate succinimidyl ester (CFDA-SE

130 Platelets labeled with carboxyfluorescein diacetate succinimidyl ester (CFDASE)

131 than the wild type strain, as determined by carboxyfluorescein diacetate succinimidyl ester (CFSE) l

132 l CD34(+) cells were labeled with 5-(and 6-)-carboxyfluorescein diacetate succinimidyl ester (CFSE) t

133 Blood mononuclear cells stained with carboxyfluorescein diacetate succinimidyl ester (CFSE) w

134 tected by flow cytometry after labeling with carboxyfluorescein diacetate succinimidyl ester (CFSE),

135 hogenesis, we examined migratory profiles of carboxyfluorescein diacetate succinimidyl ester (CFSE)-l

136 Carboxyfluorescein diacetate succinimidyl ester (CFSE)-s

137 taneous injection of alum adjuvant including carboxyfluorescein diacetate succinimidyl ester (CFSE).

138 pulations by using the fluorescent molecule, carboxyfluorescein diacetate succinimidyl ester (CFSE).

139 le intracytoplasmic fluorescent dye 5- and 6-carboxyfluorescein diacetate succinimidyl ester and brom

140 lood mononuclear cell suppression assays and carboxyfluorescein diacetate succinimidyl ester assays w

141 ADOR antagonists or agonists were tested in carboxyfluorescein diacetate succinimidyl ester assays.

142 il activation and CD4(+) T-cell responses by carboxyfluorescein diacetate succinimidyl ester dilution

143 assessed by proliferation (thymidine uptake, carboxyfluorescein diacetate succinimidyl ester dye dilu

144 s of cell division using the fluorescent dye carboxyfluorescein diacetate succinimidyl ester indicate

145 The pretreated Lewis(BN) lymphocytes were carboxyfluorescein diacetate succinimidyl ester labeled

146 lococcus enterotoxin B was determined by the carboxyfluorescein diacetate succinimidyl ester measurem

147 responses were studied by thymidine uptake, carboxyfluorescein diacetate succinimidyl ester staining

148 CD4-cell proliferation, the fluorescein dye carboxyfluorescein diacetate succinimidyl ester was used

149 acellular fluorescent marker CFSE (5-(and-6)-carboxyfluorescein diacetate succinimidyl ester) to trac

150 amine-reactive fluorescent label, 5-(and-6)-Carboxyfluorescein Diacetate Succinimidyl Ester, and siz

151 FITC-based membrane-binding dye, 5-(and -6)-carboxyfluorescein diacetate succinimidyl ester, to allo

152 T cells were 5-(and-6-)-carboxyfluorescein diacetate succinimidyl ester- (CFSE)

153 roliferating responder cells was assessed in carboxyfluorescein diacetate succinimidyl ester-based as

154 adhesion was measured by the retention of 5-carboxyfluorescein diacetate succinimidyl ester-labeled

155 Flow cytometric analysis of carboxyfluorescein diacetate succinimidyl ester-labeled

156 ation of donor CD8+ T-cells in recipients of carboxyfluorescein diacetate succinimidyl ester-labeled

157 o recruit adoptively transferred 5- (and -6)-carboxyfluorescein diacetate succinimidyl ester-labeled

158 Transfer of 5,6-carboxyfluorescein diacetate succinimidyl ester-labeled

159 r to T cell-deficient host mice by injecting carboxyfluorescein diacetate succinimidyl ester-labeled

160 Phagocytosis of human carboxyfluorescein diacetate succinimidyl ester-labeled

161 Carboxyfluorescein diacetate succinimidyl ester-labeled

162 n vivo were assessed by adoptive transfer of carboxyfluorescein diacetate succinimidyl ester-labeled

163 In separate experiments, 5- (and 6)-carboxyfluorescein diacetate succinimidyl ester-labeled

164 the proliferation of adoptively transferred carboxyfluorescein diacetate succinimidyl ester-labeled

165 The proliferation capacities of carboxyfluorescein diacetate succinimidyl ester-positive

166 -bromo-2'-deoxyuridine)- and CFSE [5-(and 6)-carboxyfluorescein diacetate succinimidyl ester]-labeled

167 collagenase perfusion and labeled using 5(6)-carboxyfluorescein diacetate succinimidyl-ester (CMFSE).

168 ve found that sorted CFSE(bright) (5-(and-6)-carboxyfluorescein diacetate succinmidyl ester) (nondivi

169 that were loaded with the fluorogenic dyes - carboxyfluorescein diacetate, Oregon green carboxylic ac

170 Yet the reagent, carboxyfluorescein diacetate, still possesses a free car

171 valuated using 3H-thymidine (3H-TdR) uptake, carboxyfluorescein diacetate, succinimidyl ester (CFDA-S

172 hly isolated NK cells labeled with 5-(and-6)-carboxyfluorescein diacetate, succinimidyl ester (CFSE)

173 Adoptive transfer of carboxyfluorescein diacetate, succinimidyl ester (CFSE)-

174 Carboxyfluorescein diacetate, succinimidyl ester-labeled

175 ation was visualized by adoptive transfer of carboxyfluorescein diacetate, succinimidyl ester-labeled

176 loem-export assay with the symplastic tracer carboxyfluorescein diacetate.

177 Carboxyfluorescein-diacetate succinimidyl ester-labeled

178 n peripheral blood mononuclear cells using a carboxyfluorescein-diacetate-succinimidylester (CFSE) di

179 (GO) as quencher, where an amino and FAM (6-carboxyfluorescein) dual labeled DNA was covalently atta

180 ne) bilayer vesicles encapsulating 5-(and-6)-carboxyfluorescein dye showed that apoE4 remodeled and d

181 Carboxyfluorescein efflux and lipid flip-flop occur with

182 In BSM/Chol/POPC vesicles the rate of carboxyfluorescein efflux induced by delta-lysin increas

183 The kinetics of carboxyfluorescein efflux induced by the amphipathic pep

184 ylcholine (POPC) on the basis of kinetics of carboxyfluorescein efflux induced by the amphipathic pep

185 In view of this finding, carboxyfluorescein efflux kinetics were re-examined.

186 The rate of 6-carboxyfluorescein elimination from the aqueous humor of

187 s), and (iv) the dyes chosen as the donor (6-carboxyfluorescein, F; or 3-(epsilon-carboxypentyl)-3'-e

188 1,3-dipolar cycloaddition between alkynyl 6-carboxyfluorescein (FAM) and azido-labeled single-strand

189 Thus, a primer that carries 6-carboxyfluorescein (FAM) at the 5'-end and 6-carboxy-4',

190 Similar results were obtained with 6-carboxyfluorescein (FAM)-conjugated peptides and western

191 The synthetic 5-(and-6)-carboxyfluorescein(FAM)-RGRSWpTY-COOH peptide, when boun

192 tto488 (emitting at the same wavelength as 6-carboxyfluorescein, FAM) and Atto467N (emitting at the s

193 Anti-TAR 3'-carboxyfluorescein- (FAM-) labeled OMe and OMe/LNA chime

194 owed by monitoring the fluorescence from a 6-carboxyfluorescein (FAM6) fluorophore covalently linked

195 The reporter probes are tagged with carboxyfluorescein-filled liposomes.

196 cells and by 2'-7'-bis[2-carboxymethyl]-5(6)-carboxyfluorescein fluorescence measuring the accelerate

197 -derived mesenchymal cells are identified by carboxyfluorescein fluorescence with confocal microscopy

198 , and pH was measured with bis(carboxyethyl)-carboxyfluorescein fluorescence-conjugated dextran.

199 and the release of contents was followed by carboxyfluorescein fluorescence.

200 indicator of caspase-1 activity (FAM-FLICA [carboxyfluorescein-fluorochrome-labeled inhibitors of ca

201 or West Nile virus (WNV) detection using a 6-carboxyfluorescein fluorophore and TaqMan for internal c

202 e labeled with different fluorescent dyes (6-carboxyfluorescein for gG2 and 6-hexachlorofluorescein f

203 haracterized the encapsulation efficiency of carboxyfluorescein for vesicles prepared by rotary evapo

204 The release of carboxyfluorescein from large unilamellar vesicles compo

205 g whether the ceramides induced leakage of 6-carboxyfluorescein from lipid vesicles.

206 demonstrated by the cellular uptake of 5(6)-carboxyfluorescein from the culture medium when extracel

207 han 100,000-fold improvement in detection of carboxyfluorescein in 8 min.

208 They contained carboxyfluorescein in the aqueous core and fluorescein-l

209 ndicator of live bacteria is a caged form of carboxyfluorescein in which 3' and 6' hydroxyl groups ar

210 ye BCECF [2',7'-bis-(carboxyethyl)-5-(and-6)-carboxyfluorescein] in wide-field and confocal microscop

211 Injection of carboxyfluorescein into muscles of the posterior pharynx

212 -sensitive dye 2', 7'-bis(carboxyethyl)-5(6)-carboxyfluorescein; intracellular pH (pHi) was measured

213 th confocal microscopy and by membrane-bound carboxyfluorescein isolation bodies with electron micros

214 cent dye 4',5'-dichloro-2',7'-dimethoxy-5(6)-carboxyfluorescein (JOE) is reported; the overall yield

215 l substrate is a tetranucleotide with a 5',6-carboxyfluorescein label (6-FAM) and a 3',6-carboxy-tetr

216 emonstrated that DDT1 MF2 cells internalized carboxyfluorescein-labeled (FAM) AO within 30 min.

217 Carboxyfluorescein-labeled brain tubulin has been microi

218 The 6-carboxyfluorescein-labeled DNA fragments were detected w

219 Results of a fluorescence assay of LF on carboxyfluorescein-labeled liposomes composed of phospha

220 Carboxyfluorescein-labeled peptides were used to determi

221 single multiplex PCR while incorporating a 6-carboxyfluorescein-labeled universal primer to fluoresce

222 ASBA-ECL assay) and a real-time assay with 6-carboxyfluorescein-labeled virus-specific molecular beac

223 larization (CNV) by injecting heat-sensitive carboxyfluorescein liposomes intravenously, locally rele

224 s, was administered intravenously along with carboxyfluorescein liposomes.

225 e protein from SMs and reconstituted it into carboxyfluorescein-loaded liposomes for transport studie

226 P = 0.0039), dexamethasone (P = 0.0001), and carboxyfluorescein (P = 0.0016).

227 (P = 0.0004), dexamethasone (P<0.0001), and carboxyfluorescein (P = 0.0064) at elevated intraocular

228 After labeling medial edge epithelia with carboxyfluorescein, palatal shelves (E8-9) with or witho

229 The carboxyfluorescein permeability of Cys-less hemichannels

230 thiol modification of the Cys abolishes the carboxyfluorescein permeability.

231 al stimulation increased open probability of carboxyfluorescein-permeable membrane channels.

232 Bcl-2, in contrast, triggered carboxyfluorescein release at acidic pH only.

233 orescence with two types of experiments: (a) carboxyfluorescein release from the vesicles upon peptid

234 ynamic (incorporation isotherm) and kinetic (carboxyfluorescein release) studies.

235 -isothiocyanate, fluorescein disodium, and 5-carboxyfluorescein, respectively, relative to a traditio

236 fluorescence of Trp, or vesicle-encapsulated carboxyfluorescein, respectively.

237 fluorescent dye 2'-7'-bis(carboxyethyl)-5,6-carboxyfluorescein so that changes in intracellular pH (

238 ule (CD31), pan-leukocyte protein (CD45), or carboxyfluorescein succiminidyl ester (CFSE) fluorescenc

239 using tritiated thymidine incorporation and carboxyfluorescein succinimidyl ester (CFSE) dilution ex

240 d assay Jkt cell division was evaluated with carboxyfluorescein succinimidyl ester (CFSE) fluorescent

241 The infected cells could be divided into 2 carboxyfluorescein succinimidyl ester (CFSE) groups, CFS

242 s measured by dilution of the intravital dye carboxyfluorescein succinimidyl ester (CFSE) in 3- to 4-

243 CD107(a/b) degranulation, and CD4(+) T cell carboxyfluorescein succinimidyl ester (CFSE) proliferati

244 We assessed CAR-T cell cytotoxicity using a carboxyfluorescein succinimidyl ester (CFSE) release ass

245 We developed a carboxyfluorescein succinimidyl ester (CFSE)-based flow-

246 Additional flow cytometry studies measuring carboxyfluorescein succinimidyl ester dilution and intra

247 ed by (3)H thymidine incorporation assay and carboxyfluorescein succinimidyl ester dilution assay.

248 We showed by the carboxyfluorescein succinimidyl ester dilution method th

249 assays (based on thymidine incorporation and carboxyfluorescein succinimidyl ester dilution).

250 measured by thymidine incorporation and 5,6-carboxyfluorescein succinimidyl ester dilution.

251 6A induces cell division, as measured by 5,6-carboxyfluorescein succinimidyl ester dye and flow cytom

252 sured by intracellular cytokine staining and carboxyfluorescein succinimidyl ester dye dilution.

253 ntigen-stimulated cultures as ascertained by carboxyfluorescein succinimidyl ester loading.

254 islets were surrounded by MSCs labeled with carboxyfluorescein succinimidyl ester or Qdot nanocrysta

255 sed assessment of autoantibody formation and carboxyfluorescein succinimidyl ester proliferation stud

256 iferation was quantified by cytometry, using carboxyfluorescein succinimidyl ester staining or micros

257 rmined by enzyme-linked immunosorbent assay, carboxyfluorescein succinimidyl ester staining, and cyto

258 o peripheral lymphoid organs was verified by carboxyfluorescein succinimidyl ester staining, and HA-s

259 uorophores, fluorescein isothiocyanate and 5-carboxyfluorescein succinimidyl ester, to effectively la

260 rize the T cells reactive to HIPs, we used a carboxyfluorescein succinimidyl ester-based assay to clo

261 Flow cytometry of HCV-infected carboxyfluorescein succinimidyl ester-labeled hepatoma c

262 ly generated CD4+ CD25(high) FOXP3+ Tregs in carboxyfluorescein succinimidyl ester-labeled MLR respon

263 Finally, experiments using carboxyfluorescein succinimidyl ester-labeled T cells ad

264 )H-thymidine incorporation as well as by the carboxyfluorescein-succinimidyl ester method of cell div

265 Using transfer of carboxyfluorescein succinyl ester (CFSE)-labeled T-cell

266 t low pH and in low dielectric media while 3-carboxyfluoresceins tend to lactonize.

267 ining a membrane-impermeant fluorescent dye (carboxyfluorescein), the peptide permeabilizes the outer

268 response of 2', 7'-bis(2-carboxyethyl)-5(6)-carboxyfluorescein to H+ were the same in all cell lines

269 ated that the proximity of the chromophore 6-carboxyfluorescein to the 2-nitrobenzyl linker did not h

270 y, a similar fraction of germline injected 5-carboxyfluorescein transfers to the intestine, demonstra

271 membrane-impermeable fluorescent molecule, 5-carboxyfluorescein, transfers to the germline after its

272 Significantly increased corneal carboxyfluorescein uptake was noted in the scop patch gr

273 was assessed by fluorometric measurement of carboxyfluorescein uptake.

274 ] at the 5' end with 4,7,2',7'-tetrachloro-6-carboxyfluorescein) using HaeIII and BstEII and of a 475

275 (labeled [both strands] at the 5' end with 6-carboxyfluorescein) using HaeIII and CfoI.

276 Carboxyfluorescein was encapsulated in heat-sensitive li

277 ECF (1,2',7'-bis(2-carboxyethyl)-5-(and -6-)-carboxyfluorescein) was included in microinjectate, and

278 Fluorescein sodium and carboxyfluorescein were then used as low molecular weigh

279 tracer substrates 5-carboxyfluorescein and 6-carboxyfluorescein were used.

280 by emission intensity changes of amphiphilic carboxyfluorescein, which is coembedded into the fluid D

281 apsulating high concentration, self-quenched carboxyfluorescein, which is released by the lysis of th

282 Parallel separations of fluorescein and carboxyfluorescein yielded less than 3% relative standar