ライフサイエンスコーパス: carboxyfluorescein

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

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

3 These heterotypic channels were permeable to carboxyfluorescein.

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

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

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

7 cohol) layer contains the self-quenching dye 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 TP filter was used to enhance detection of 6-carboxyfluorescein 4-fold over fluorescein, even though

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

37 Confocal analysis with carboxyfluorescein-alendronate confirmed the microcalcif

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

87 5' labeled with fluorescent probes such as 6-carboxyfluorescein can be rapidly separated and quantifi

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

115 Injection of carboxyfluorescein diacetate succinimide ester-labeled C

116 Platelets labeled with carboxyfluorescein diacetate succinimidyl ester (CFDASE)

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

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

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

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

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

122 Carboxyfluorescein diacetate succinimidyl ester (CFSE)-s

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

139 Flow cytometric analysis of carboxyfluorescein diacetate succinimidyl ester-labeled

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

141 Phagocytosis of human carboxyfluorescein diacetate succinimidyl ester-labeled

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

143 Carboxyfluorescein diacetate succinimidyl ester-labeled

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

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

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

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

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

149 The proliferation capacities of carboxyfluorescein diacetate succinimidyl ester-positive

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

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

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

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

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

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

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

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

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

159 Carboxyfluorescein diacetate, succinimidyl ester-labeled

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

161 Carboxyfluorescein-diacetate succinimidyl ester-labeled

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

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

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

165 Carboxyfluorescein efflux and lipid flip-flop occur with

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

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

168 The kinetics of carboxyfluorescein efflux induced by the amphipathic pep

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

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

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

172 1,3-dipolar cycloaddition between alkynyl 6-carboxyfluorescein (FAM) and azido-labeled single-strand

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

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

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

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

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

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

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

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

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

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

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

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

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

186 The release of carboxyfluorescein from large unilamellar vesicles compo

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

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

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

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

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

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

193 Injection of carboxyfluorescein into muscles of the posterior pharynx

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

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

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

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

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

199 Carboxyfluorescein-labeled brain tubulin has been microi

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

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

202 Carboxyfluorescein-labeled peptides were used to determi

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

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

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

206 s, was administered intravenously along with carboxyfluorescein liposomes.

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

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

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

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

211 The carboxyfluorescein permeability of Cys-less hemichannels

212 thiol modification of the Cys abolishes the carboxyfluorescein permeability.

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

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

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

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

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

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

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

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

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

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

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

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

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

226 We showed by the carboxyfluorescein succinimidyl ester dilution method th

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

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

229 6A induces cell division, as measured by 5,6-carboxyfluorescein succinimidyl ester dye and flow cytom

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

245 was assessed by fluorometric measurement of carboxyfluorescein uptake.

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

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

248 Carboxyfluorescein was encapsulated in heat-sensitive li

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

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

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

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

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