ライフサイエンスコーパス: diacetate

1 chavibetol acetate and 4-allyl-1,2-phenylene diacetate).

2 mino-5-methylamino-2',7'-difluorofluorescein diacetate).

3 using 2',7'-dichloroflorescin diacetate (DCF-diacetate).

4 e determined using 2',7'-dichlorofluorescein diacetate.

5 5-(and -6)-carboxy 2',7'-dichlorofluorescein diacetate.

6 itive fluorescent marker, diaminofluorescein diacetate.

7 5,6-carboxy-2',7'-dihydrodichlorofluorescein diacetate.

8 n the enantiotopic C-O single bonds of a gem-diacetate.

9 s was measured with 2',7'-dichlorofluorescin diacetate.

10 cells with 51Cr or 5-chloromethylfluorescein diacetate.

11 fluorescent probe, 2',7'-dichlorofluorescein diacetate.

12 ation of preloaded 2',7'-dichlorofluorescein diacetate.

13 4-amino-5-methylamino-2',7'-difluororescein diacetate.

14 ith the symplastic tracer carboxyfluorescein diacetate.

15 ere measured using 2',7'-dichlorofluorescein diacetate.

16 er molecule 2',7'-dichlorodihydrofluorescein diacetate.

17 -yl acetates through the intermediacy of gem-diacetates.

18 ing) to test the efficacy of a chlorhexidine diacetate 10% weight per volume (w/v) dental coating (CH

19 or 2,3-diallyl-5,6-dimethyl-1,4-hydroquinone diacetate (16) formed silylated fused bicyclic complexes

20 Acetylation of the diacetate 2 followed by acid-catalyzed elimination and r

21 eta)-3-hydroxycholestane-4,6-diene-1,25-diol diacetate (2) is described.

22 nsfer enzymes leads to an optimized match of diacetate 20 with PPL.

23 enzymatic desymmetrization of advanced meso diacetate 20, through PPL-mediated ester hydrolysis.

24 Racemic diacetate 21 showed a strong activity against KB-3-1 cel

25 C-3 in diltiazem, the 3-monoacetate (8) and diacetate (3) derivatives of 2 were prepared.

26 were also labeled with 6-carboxyfluorescein diacetate (6-CFDA) as an internal standard.

27 e transport kinetics of 6-carboxyfluorescein diacetate (6-CFDA), which is processed in hepatocytes in

28 poxy bisketal 6 or the 5 alpha,6 alpha-epoxy diacetate 7 followed by dehydration of the 6 beta-propar

29 l [(+/-)-7], into enantiomerically pure (+)-diacetate 8 and (-)-monoacetate 9.

30 symmetric allylic alkylation reaction of gem-diacetate 9 with azlactone 10.

31 omo isomers were isolated as the ring closed diacetates 9b and 11 by fractional crystallization.

32 r both FM4-64 and carboxydichlorofluorescein diacetate (a vacuolar luminal vital stain), had a pronou

33 4,5-diaminofluorescein diacetate, a cell-permeable fluorescent molecule, was us

34 Using dichlorofluorescein diacetate, a detector of endogenous oxidative stress, it

35 loromethyl-2',7'-dichlorodihydrofluorescence diacetate acetyl ester (CM-H(2)DCFDA) assay.

36 hloromethyl-2',7'-dichlorodihydrofluorescein diacetate, acetyl ester (CM-H2-DCFDA).

37 chlormethyl-2',7'-dichlorodihydrofluorescein diacetate, acetyl ester (CM-H2DCF-DA), and high levels p

38 loromethyl-2',7'-dichlorodihydrofluorescence diacetate, acetyl ester assay, respectively.

39 hloromethyl-2',7'-dichlorodihydrofluorescein diacetate, acetyl ester in preloaded neutrophils.

40 chloromethyl-2',7'-dichlorodihydrofluorescin diacetate, acetyl ester, in a concentration- and time-de

41 ndividual carotenoid molecules, while lutein diacetate aggregates resemble nematic liquid crystals.

42 sorption and CD spectra of lutein and lutein diacetate aggregates, which have previously been describ

43 In addition, the separated 2,4-diacetates also provide short access to all four anomeri

44 at were loaded with diaminofluorofluorescein diacetate, an intracellular fluorescence probe for NO, e

45 orescence microscopy with diaminofluorescein diacetate, an NO probe, and Fluo-3, a Ca(2+) probe.

46 ifferences in 2'7'dichlorodihydrofluorescein diacetate and 4,5-diaminofluorescein diacetate fluoresce

47 oxidative stress (2',7'-dichlorofluorescein-diacetate and Amplex Red analysis), and phagocytosis (St

48 through ligand exchange between iodobenzene diacetate and arylglyoxylic acid to initiate the cascade

49 fluorescent NO probe 4,5-diaminofluorescein diacetate and by the 2,3-diaminonaphthalene method.

50 determined using dichlorodihydrofluorescence diacetate and cytochrome c, were rapidly and significant

51 Only a few nanograms per liter of ethynodiol diacetate and desogestrel in water would be needed for f

52 mino,4-aminomethyl-2',7'-difluorofluorescein diacetate and diamino-rhodamine-4M, respectively.

53 oxidation of both dichlorodihydrofluorescein diacetate and dihydroethidium.

54 hloromethyl-2',7'-dichlorodihydrofluorescein diacetate and dihydrorhodamine 123, respectively.

55 oth the enantiotopic leaving groups of a gem-diacetate and enantiotopic faces of the enolate of an az

56 l microbiota using 2',7'-dichlorofluorescein diacetate and flow cytometry.

57 fluorescent probe 2',7'-dichlorofluorescein diacetate and flow cytometry.

58 AcT and its two substrates, propylene glycol diacetate and H(2)O(2), sufficient and continuous PAA is

59 e fluorescent probe 2',7'-dichlorofluorescin diacetate and laser-scanning confocal microscopy.

60 e 5, which upon treatment with iodosobenzene diacetate and magnesium oxide in the presence of a rhodi

61 mino-5-methylamino-2',7'-difluorofluorescein diacetate, and this effect was reversed by SR141716A.

62 new microplate assays utilizing fluorescein diacetate as a live cell stain and erythrosine B as a de

63 Using dichlorodihydrofluorescein diacetate as a probe, we found that the NQO1 transfectan

64 (DKR) protocols were developed using geminal diacetate as an acylating agent, resulting in chiral ace

65 bacterial esterase staining with fluorescein diacetate as well as colony-forming unit counts from inf

66 ed by a fluorescent 2',7'-dichlorofluorescin diacetate assay, and >85% reduction in HIF2-alpha mRNA a

67 totoxicity, 2',7'-dichlorodihydrofluorescein diacetate assay, and Western blot were used to investiga

68 duction determined by the dichlorofluorescin diacetate assay.

69 panetricarboxylate), or CDA (1,1-cyclohexane diacetate) at pH values between 7 and 8 yields baroresis

70 ponding N-hydroxy compounds with iodobenzene diacetate, [bis(trifluoroacetoxy)]iodobenzene, and ammon

71 short, scalable syntheses of an L-iduronate diacetate C-4 acceptor, and also L-iduronate C-4 accepto

72 ye, carboxy-H(2)-dichloro-dihydrofluorescein diacetate (carboxy-H(2)-DCFDA), to determine whether ROS

73 Cellulose diacetate (CDA), a biobased material widely used in cons

74 l degradation of fabrics made from cellulose diacetate (CDA), a biobased polymer used commonly in con

75 5-(and 6)-carboxy-2',7'-dichlorofluorescein diacetate (CDCFDA).

76 ime-dependent decrease in carboxyfluorescein diacetate (CFDA) fluorescence was then quantitatively an

77 The fluorescent probes, carboxyfluorescein diacetate (CFDA) for cytoplasmic esterase activity and d

78 hloromethyl-2',7'-dichlorodihydrofluorescein diacetate (CM-H(2)DCFDA), spin-trap electron paramagneti

79 TC-GC) and carboxy-4',5'-dimethylfluorescein diacetate (CMFD), which are fluorescent substrates for t

80 the organic anion 5-chloromethylfluorescein diacetate (CMFDA) was reduced in KO hepatocytes, as well

81 stoichiometric neptunyl(VI) and plutonyl(VI) diacetate compounds that can serve as starting materials

82 effectively controlled by the chlorhexidine diacetate content and pH.

83 terium tuberculosis labeled with fluorescein diacetate could be accomplished rapidly by using flow cy

84 (6-amidoethyl)triphenylphosphonium Zinpyr-1 diacetate (DA-ZP1-TPP), is essentially nonfluorescent in

85 mino-5-methylamino-2',7'-difluorofluorescein diacetate (DAF) as a fluorescent NO-sensor that locates

86 fluorescent indicator 4,5-diaminofluorescein diacetate (DAF-2 DA) during stimulation of the cervical

87 cific fluorescent dye 4,5-diaminofluorescein diacetate (DAF-2 DA) were treated with lysophosphatidic

88 membrane-permeable dye diaminofluorescein-2/diacetate (DAF-2/DA) that, once intracellular, bound NO

89 NO detection system, 4,5-Diaminofluorescein diacetate (DAF-2/DA), for the direct detection of NO pro

90 itric oxide indicator 4,5-diaminofluorescein diacetate (DAF-2DA) specifically labels the bulbus arter

91 use of fura 2-AM and 4,5-diaminofluorescein diacetate (DAF-2DA), respectively, in microtissue strips

92 luorescence probe diaminodifluorofluorescein diacetate (DAF-FM DA), and the subsequent fluorescent DA

93 luorescence probe diaminodifluorofluorescein diacetate (DAF-FM DA), and the subsequent NO production

94 mino-5-methylamino-2',7'-difluorofluorescein diacetate (DAF-FM DA).

95 mino-5-methylamino-2',7'-difluorofluorescein diacetate (DAF-FM DA).

96 mino-5-methylamino-2',7'-difluorofluorescein diacetate (DAF-FM), we visualized NO production in indiv

97 assessed by 2',7'-dichlorodihydrofluorescein diacetate (DCF) oxidation.

98 ating SS-RBC with 2', 7'-Dichloro-fluroescin Diacetate (DCF)-labeled PMN.

99 cence microscopy of 2',7'-dichlorofluorescin diacetate (DCF)-loaded cells showed that IL-1alpha incre

100 epG2) were quantified by dichlorofluorescein diacetate (DCF-DA) dye assay, whereas changes in express

101 metry analysis using 2',7'-dichloroflorescin diacetate (DCF-diacetate).

102 es (ROS) with the use of dichlorofluorescein diacetate (DCFDA), dihydroethidium, and cerium chloride.

103 loromethyl-2',7'-dichlorodihydro-fluorescein diacetate (DCFdA).

104 on of intracellular 2',7'-dichlorofluorescin diacetate (DCFH) dye increased under 2% O(2), indicating

105 cal microscopy with 2',7'-dichlorofluorescin diacetate (DCFH) or using electron microscopy with ceriu

106 ing microscopy, using 2,7-dichlorofluorescin diacetate (DCFH-DA) as a probe.

107 dative stress using 2',7'-dichlorofluorescin diacetate (DCFH-DA) fluorescence.

108 cein AM assay, and 2',7'-dichlorofluorescein diacetate (DCFH-DA) was used to determine intracellular

109 ment procedures with compound 37 yielded the diacetate derivative 39.

110 Uranyl diacetate dihydrate is a useful reagent for the preparat

111 uorescent probes (dichlorodihydrofluorescein diacetate, dihydroethidium, and MitoSOX Red) in conjunct

112 g the fluorescent probes dichlorofluorescein diacetate, dihydrorhodamine 123, and 2,3-diaminonapthale

113 acrocycle 1,4,7,10-tetraazacyclododecane-1,7-diacetate (DO2A) to the corresponding lanthanide aquo io

114 isting of 1,4,7,10-tetraazacyclododecane-1,7-diacetate (DO2A) was constructed with the goal of improv

115 sured with 2',7'-dicholorodihydrofluorescein diacetate dye assay.

116 was assayed using 2',7'-dichlorofluorescein diacetate dye, inducible nitric oxide synthase levels de

117 asured with 2',7'-dichlorodihydrofluorescein diacetate dye.

118 aldehydes in the presence of ethylenediamine diacetate (EDDA) is reported.

119 were measured with 2', 7'-dichlorofluorescin diacetate; emissions of the oxidized product were detect

120 ad Candida in the coculture with fluorescein diacetate (FDA) and propidium iodide (PI), respectively,

121 increase in the fluorescence of fluorescein diacetate (FDA) by 30 and 42%, suggesting a decrease in

122 The fluorescein diacetate (FDA) stained onion adaxial epidermis showed d

123 antituberculosis agents by using fluorescein diacetate (FDA) staining and flow cytometry.

124 assessed sputum microscopy with fluorescein diacetate (FDA, evaluating M. tuberculosis metabolic act

125 easured as an increase in dichlorofluorescin diacetate fluores-cence) and that similar changes were n

126 OI)-induced 2',7'-dichlorodihydrofluorescein diacetate fluorescence and Northern blot analysis of hem

127 rescein diacetate and 4,5-diaminofluorescein diacetate fluorescence levels.

128 mino-5-methylamino-2',7'-difluorofluorescein diacetate fluorescence mainly determined NO production,

129 mino,4-aminomethyl-2',7'-difluorofluorescein diacetate fluorescence originated from mitochondria.

130 The 2,7-dichlorodihydrofluorescein diacetate fluorescence test demonstrated that the fracti

131 R-stimulated increase in dichlorofluorescein diacetate fluorescence was abolished with catalase but r

132 increase in 2',7'-dichlorodihydrofluorescein diacetate fluorescence, whereas TGO500 and TGO800 induce

133 ation, assessed from 2,7-dichlorofluorescein diacetate fluorescence.

134 ecies were measured with dichlorofluorescein diacetate fluorescence.

135 cells was labeled with tetra-methylrhodamine diacetate followed by the formation of tumor cell-neutro

136 mino-5-methylamino-2',7'-difluorofluorescein diacetate for NO activity in isolated mesenteric resista

137 ime ester (23d) with a polymer-bound iodosyl diacetate gave the spiroisoxazoline (24) and represents

138 assay and 2',7'-dicholorodihydrofluorescein diacetate (H(2)DCFDA) dye assay, respectively.

139 hloromethyl-2',7'-dichlorodihydrofluorescein diacetate (H(2)DCFDA) probe and flow cytometry.

140 etry using 2', 7'-dichlorodihydrofluorescein diacetate (H(2)DCFDA) showed an increase in oxidative st

141 xidation of 2',7'-dichlorodihydrofluorescein diacetate (H2DCFDA) by human 5-LOX.

142 e assay and 2',7'-dichlorodihydrofluorescein diacetate (H2DCFDA) dye assay, respectively.

143 Geminal diacetates have been used as sustainable acyl donors for

144 se, arylsulfatase activities and fluorescein diacetate hydrolysis-FDA).

145 ecies (ROS) probe dichlorodihydrofluorescein diacetate (i.e. H(2) DCFDA-staining) coupled with flow c

146 -4H-pyrans was accomplished with iodobenzene diacetate (IBD) and N-chlorosuccinimide (NCS) reagents i

147 3), DDQ, CAN, [Cp(2)Fe][PF(6)], phenyliodine diacetate, IBX).

148 orescence of 2',7'-dihydrodichlorofluorescin diacetate in HAEC, an indicator of ROS production.

149 dant sensitive dye 2',7'-dichlorofluorescein diacetate in murine macrophage J774.1 cells.

150 ng difluoroacetic acid and phenyliodine(III) diacetate in tetrahydrofuran under visible-light activat

151 nes from styrenes mediated by phenyliodonium diacetate in the presence of molecular oxygen and N-hydr

152 xidation-sensitive probe, dihydrofluorescein diacetate, indicating a shift in the intracellular redox

153 ellular activation of PKC with phorbol 12,13-diacetate induced a pharmacological potentiation of the

154 the fluorescent tracer 5-carboxyfluorescein diacetate into the cytoplasm, and quantified its interce

155 ocytes to metabolize and excrete fluorescein diacetate into visible bile canaliculi.

156 escence NO indicator (4,5-diaminofluorescein diacetate), intracellular NO was measured in the endothe

157 (-)-cryptocaryolone and (-)-cryptocaryolone diacetate is presented herein.

158 DCFH2-DA (2',7'-dichlorodihydrofluorescein diacetate) is the most widely used fluorogenic probe for

159 A fructose-derived diacetate ketone has been shown to be an effective catal

160 l-Glutamate-N,N-diacetate (L-GLDA) was recently introduced in the United

161 CellTracker Green 5-chloromethylfluorescein diacetate-labeled cytosol to ascertain whether cytosol w

162 d chemiluminescence) and elevated NO (DAF-FM diacetate) levels in NOS1(-/-) myocytes.

163 Phenyliodine(III) diacetate -mediated 1,2-ipso-migration of an imidazo[1,2

164 quantitated by the 2',7'-dichlorofluorescein diacetate method.

165 S; mitosox red and 2',7'-dichlorofluorescein diacetate), NADPH, NADP(+) and ATP contents (spectrophot

166 doxybenzoate can be further converted to the diacetate or a bis(trifluoroacetate) derivative by treat

167 ns of a palladium catalyst and iodosobenzene diacetate or copper(II) salts, respectively, represent t

168 of hypervalent iodine reagents (phenyliodine diacetate or Dess-Martin periodinane) allows the rapid a

169 5-carboxyl group from 5-carboxy-fluorescein diacetate or from Oregon green diacetate or from Oregon

170 y-fluorescein diacetate or from Oregon green diacetate or from Oregon green diacetoxymethylester are

171 rwent oxidative cyclization with iodobenzene diacetate or iodosobenzene in the presence of Rh2(OAc)4,

172 rogen (OR, 2.7; 95% CI, 1.1-6.2), ethynodiol diacetate (OR, 2.6; 95% CI, 1.4-4.7), or triphasic dosin

173 cein diacetate, Oregon green carboxylic acid diacetate, or Calcein AM.

174 on using hydroethidine, dicarboxyfluorescein diacetate, or MitoSOX.

175 th the fluorogenic dyes - carboxyfluorescein diacetate, Oregon green carboxylic acid diacetate, or Ca

176 (1S,2S)-, or cis-1,2-diaminocyclohexane; X = diacetate, oxalate, malonate, methylmalonate, cyclobutan

177 nitric oxide [NO] via 4,5-diaminofluorescein diacetate oxidation).

178 sured by the rates of 2,7-dichlorofluorescin diacetate oxidation.

179 mixture dibutyryl cAMP (Bt(2)cAMP) + phorbol diacetate (PDA) stimulated the p38, c-jun NH(2)-terminal

180 al mixture (dibutyryl (Bt2)cAMP plus phorbol diacetate (PDA)) induces promoters I.3/II.

181 In control slices, Mg(2+) and phorbol 12,13-diacetate (PDAc), a protein kinase C activator, strongly

182 ines has been developed using phenyliodonium diacetate (PIDA) and ammonia.

183 ions between anilide 1 and phenyliodine(III) diacetate (PIDA) through hypervalent iodine mediated C(s

184 For the initiator phenyliodine(III) diacetate (PIDA), voltammetric data demonstrate that the

185 nveniently constructed via phenyliodine(III) diacetate (PIDA)-mediated intramolecular oxidative annul

186 A phenyliodine(III) diacetate (PIDA)-mediated, highly efficient and tandem a

187 ene (PhIO) or the combination of iodobenzene diacetate (PIDA)/molecular iodine (I2), under mild react

188 xcitotoxicity was measured using fluorescein diacetate/propidium iodide (FDA/PI) cell viability assay

189 not affect islet viability (>90% fluorescein diacetate/propidium iodide) or the insulin secretion pro

190 Islet equivalents viability (fluorescein diacetate/propidium iodide), morphology, and dynamic glu

191 tative viability microscopy with fluorescein diacetate, quantitative culture, and acid-fast auramine

192 olving the stable and recyclable iodobenzene diacetate reagent are compatible with a range of NH-free

193 Phorbol 12,13-diacetate reduced VEGF mRNA levels while down-regulating

194 nd 4-amino-5-methylamino-2',7'-difluorescein diacetate, respectively, using fluorescence microscopy.

195 s hydroethidine and 2',7'-dichlorofluorescin diacetate, respectively, were used to monitor the intrac

196 r, it was shown that acylation using geminal diacetates resulted in remarkable regioselectivity by di

197 th the NO-imaging probe diaminofluorescein 2 diacetate revealed that UVA-induced NO release occurs in

198 Especially, it was revealed that geminal diacetates showed higher reactivity than vinyl acetate f

199 attributed to the increase of chlorhexidine diacetate solubility at lower pH.

200 es the formation of mobile clusters of metal diacetate species that drive extensive metal nanoparticl

201 ative burst activity with dichlorofluorescin diacetate staining) and adhesion (integrin cell surface

202 Yet the reagent, carboxyfluorescein diacetate, still possesses a free carboxyl group whose i

203 se-catalyzed enzymatic desymmetrization of a diacetate substrate, 10, was employed as a key component

204 orbent spot (ELISpot) and carboxyfluorescein diacetate succinimide ester (CFSE) proliferation assays

205 Injection of carboxyfluorescein diacetate succinimide ester-labeled CTL demonstrated mar

206 donors were labeled with carboxy-fluorescein diacetate succinimidyl diester dye to enable high-resolu

207 cells were stained with carboxy-fluorescein diacetate succinimidyl ester (CFDA SE), after which imag

208 lecules such as 5-(and-6)-carboxyfluorescein diacetate succinimidyl ester (CFDA-SE, hereinafter CFSE)

209 Platelets labeled with carboxyfluorescein diacetate succinimidyl ester (CFDASE) and leukocytes lab

210 n, and the generation of carboxy-fluorescein diacetate succinimidyl ester (CFSE) labeled CD4CD25FOXP3

211 strain, as determined by carboxyfluorescein diacetate succinimidyl ester (CFSE) labeling of the cell

212 lation was determined by carboxy-fluorescein diacetate succinimidyl ester (CFSE) staining and ELISA a

213 divided, as evaluated by carboxyfluoresccin diacetate succinimidyl ester (CFSE) staining.

214 e labeled with 5-(and 6-)-carboxyfluorescein diacetate succinimidyl ester (CFSE) to track cell divisi

215 uclear cells stained with carboxyfluorescein diacetate succinimidyl ester (CFSE) were cultured with B

216 metry after labeling with carboxyfluorescein diacetate succinimidyl ester (CFSE), dioctadecyl-tetrame

217 , or the fluorescent dye carboxy-fluorescein diacetate succinimidyl ester (CFSE), their division hist

218 ned migratory profiles of carboxyfluorescein diacetate succinimidyl ester (CFSE)-labeled T lymphocyte

219 Carboxyfluorescein diacetate succinimidyl ester (CFSE)-stained splenocytes

220 f alum adjuvant including carboxyfluorescein diacetate succinimidyl ester (CFSE).

221 the fluorescent molecule, carboxyfluorescein diacetate succinimidyl ester (CFSE).

222 fluorescent dye 5- and 6-carboxyfluorescein diacetate succinimidyl ester and bromodeoxyuridine incor

223 ll suppression assays and carboxyfluorescein diacetate succinimidyl ester assays were used to assess

224 r agonists were tested in carboxyfluorescein diacetate succinimidyl ester assays.

225 D4(+) T-cell responses by carboxyfluorescein diacetate succinimidyl ester dilution assays.

226 by flow cytometry using carboxy-fluorescein diacetate succinimidyl ester dye and cytometric bead arr

227 ured as proliferation by carboxy-fluorescein diacetate succinimidyl ester dye dilution and cytokine s

228 ration (thymidine uptake, carboxyfluorescein diacetate succinimidyl ester dye dilution) and cytotoxic

229 using the fluorescent dye carboxyfluorescein diacetate succinimidyl ester indicated that imatinib mes

230 ewis(BN) lymphocytes were carboxyfluorescein diacetate succinimidyl ester labeled and adoptively tran

231 iferation, as defined by 5-carboxyfluoresein diacetate succinimidyl ester labeling, or an increase in

232 n B was determined by the carboxyfluorescein diacetate succinimidyl ester measurement of division.

233 died by thymidine uptake, carboxyfluorescein diacetate succinimidyl ester staining, and Luminex techn

234 tion, the fluorescein dye carboxyfluorescein diacetate succinimidyl ester was used.

235 were dyed with CFDA-SE (carboxy fluorescein diacetate succinimidyl ester) and labeled with (131)I-io

236 nt marker CFSE (5-(and-6)-carboxyfluorescein diacetate succinimidyl ester) to track the mitotic recor

237 of the membrane-permeable dye, Oregon Green diacetate succinimidyl ester, and a membrane-permeable b

238 orescent label, 5-(and-6)-Carboxyfluorescein Diacetate Succinimidyl Ester, and size exclusion chromat

239 e-binding dye, 5-(and -6)-carboxyfluorescein diacetate succinimidyl ester, to allow a quantitative me

240 T cells were 5-(and-6-)-carboxyfluorescein diacetate succinimidyl ester- (CFSE) labeled to allow de

241 der cells was assessed in carboxyfluorescein diacetate succinimidyl ester-based assays.

242 plex class I typing, and carboxy-fluorescein diacetate succinimidyl ester-based mixed lymphocyte resp

243 ow cytometric analysis of carboxyfluorescein diacetate succinimidyl ester-labeled B cells costained f

244 of adoptively transferred carboxyfluorescein diacetate succinimidyl ester-labeled beta-cell antigen-s

245 Carboxyfluorescein-diacetate succinimidyl ester-labeled CBA/Ca strain CD8+

246 We generated carboxy-fluorescein diacetate succinimidyl ester-labeled CD4+CD25 high FOXP3

247 Transfer of 5,6-carboxyfluorescein diacetate succinimidyl ester-labeled donor cells showed

248 T-cells in recipients of carboxyfluorescein diacetate succinimidyl ester-labeled donor T-cell infusi

249 e experiments, 5- (and 6)-carboxyfluorescein diacetate succinimidyl ester-labeled human CD4+ T cells

250 Carboxyfluorescein diacetate succinimidyl ester-labeled human platelets wer

251 6 weeks postinfection), carboxy-fluorescein diacetate succinimidyl ester-labeled naive ovalbumin-spe

252 Phagocytosis of human carboxyfluorescein diacetate succinimidyl ester-labeled platelets by PAEC/P

253 d by adoptive transfer of carboxyfluorescein diacetate succinimidyl ester-labeled T cells across a pa

254 nt host mice by injecting carboxyfluorescein diacetate succinimidyl ester-labeled T cells into mice d

255 red by the retention of 5-carboxyfluorescein diacetate succinimidyl ester-labeled T cells on FLS mono

256 y transferred 5- (and -6)-carboxyfluorescein diacetate succinimidyl ester-labeled T cells.

257 oliferation capacities of carboxyfluorescein diacetate succinimidyl ester-positive lymphocytes from t

258 ine)- and CFSE [5-(and 6)-carboxyfluorescein diacetate succinimidyl ester]-labeled lymphocytes showed

259 on and labeled using 5(6)-carboxyfluorescein diacetate succinimidyl-ester (CMFSE).

260 5-(and-6)-carboxy-2',7'-dichlorofluorescein diacetate, succinimidyl ester "mixed isomers" (CCFSE) dy

261 hymidine (3H-TdR) uptake, carboxyfluorescein diacetate, succinimidyl ester (CFDA-SE) assays; the regu

262 ls labeled with 5-(and-6)-carboxyfluorescein diacetate, succinimidyl ester (CFSE) were adoptively tra

263 Adoptive transfer of carboxyfluorescein diacetate, succinimidyl ester (CFSE)-labeled naive CD4(+

264 d by adoptive transfer of carboxyfluorescein diacetate, succinimidyl ester-labeled TEa T cell recepto

265 Carboxyfluorescein diacetate, succinimidyl ester-labeled Tg361 cells were a

266 mononuclear cells using a carboxyfluorescein-diacetate-succinimidylester (CFSE) dilution assay.

267 d CFSE(bright) (5-(and-6)-carboxyfluorescein diacetate succinmidyl ester) (nondivided) and activation

268 hloromethyl-2',7'-dichlorodihydrofluorescein diacetate that arsenite induces, within 5 min after trea

269 n the synthesis blocked the N-acetate as a N-diacetate, the N-sulfonates as azido groups, and the ami

270 The esterase converted the diacetate to chloramphenicol, thus inhibiting spirochete

271 d by oxidation of dichlorodihydrofluorescein diacetate to dichlorofluorescein and hydroethidium to et

272 f cyclohexa-2,4-diene-1,2-diylbis(methylene) diacetate to various carbasugars is described.

273 stent to demonstrate delivery of fluorescein diacetate, using applied tension, to an ex vivo esophagu

274 The former diacetate was converted to the conformationally locked (

275 e fluorochrome probe 2'7'-dichlorofluorescin diacetate was used to measure cytosolic oxidant activity

276 ve fluorescent dye, 2',7'-dichlorofluorescin diacetate, was significantly elevated in TGF-alpha/c-myc

277 OS-sensitive probe 2',7'-dichlorofluorescein diacetate, we found that antisense suppression of AOX re

278 ratios of calcium fluoride to chlorhexidine diacetate were 8/2, 5/5, and 2/8.

279 and carboxylated dichlorodihydrofluorescein diacetate were used as probes to measure mitochondrial m

280 ared by an enzymatic asymmetrization of meso-diacetate with acetyl cholinesterase, radical cyclizatio