ライフサイエンスコーパス: cyan

1 nced GFP (EGFP) spectral variants yellow and cyan.

2 ed, suggesting that these cells might be red-cyan.

3 bunit was tagged with yellow (alpha1-YFP) or cyan (alpha1-CFP) fluorescent protein.

4 .5] for mesopic, 4.93 dB [4.59, 5.27] for DA cyan and 4.02 dB [3.63, 4.42] for DA red testing.

5 coral Montipora capitata consistently emits cyan and red fluorescence across a depth gradient in ree

6 e been responsible for the generation of new cyan and red phenotypes from the ancestral green were fi

7 Mesopic, dark-adapted (DA) cyan and red sensitivities were assessed by using fundus

8 he phenyl analogue exhibits a dual emission (cyan and red) that can be used for ultrasensitive ratiom

9 nce resonance energy transfer (FRET) between cyan and yellow fluorescent (CFP/YFP) fusion proteins of

10 HSP-FRET consists of the cyan and yellow fluorescent protein fluorophores linked

11 Using cyan and yellow fluorescent protein fusion constructs, w

12 of mutant and wild-type (WT) M2 regions, of cyan and yellow fluorescent protein, and of fluorescent

13 at either the N or C termini, and a pair of cyan and yellow fluorescent protein-tagged tau were co-t

14 one another, we have constructed a tandem of cyan and yellow fluorescent proteins (CFP and YFP, respe

15 ce energy transfer (FRET) between the linked cyan and yellow fluorescent proteins (CFP and YFP, respe

16 ance energy transfer (FRET) between enhanced cyan and yellow fluorescent proteins (ECFP, EYFP) in liv

17 While pairs of cyan and yellow fluorescent proteins (FPs) are most comm

18 ains, each of which coexpresses the enhanced cyan and yellow fluorescent proteins as fusions to disti

19 luorescent resonance energy transfer between cyan and yellow fluorescent proteins conjugated at its N

20 e sensor, termed CAY, is a fusion protein of cyan and yellow fluorescent proteins flanking the peptid

21 ive variant of recombinant WNV NS2B-NS3, and cyan and yellow fluorescent proteins fused by a dodecame

22 The cyan and yellow fluorescent proteins were attached to fu

23 orescent proteins (IFPs), such as the green, cyan and yellow fluorescent proteins, have revolutionize

24 r (FRET) glutamine sensors based on improved cyan and yellow fluorescent proteins, monomeric Teal Flu

25 nce resonance energy transfer (FRET) between cyan and yellow fluorescent proteins.

26 ) between alpha- and beta- subunits fused to cyan and yellow fluorescent proteins.

27 ntaining acidic amino acid residues, between cyan and yellow mutants of GFP.

28 by sandwiching the full-length Epac1 between cyan and yellow mutants of GFP.

29 kinase (cGPK), minus residues 1-77, between cyan and yellow mutants of green fluorescent protein.

30 e resonance energy transfer (FRET) between a cyan and yellow variant of GFP fused to the termini of t

31 Next, we create cyan and yellow variants, achieving activity-dependent,

32 sfer between those two proteins labeled with cyan and yellow-green variants of green fluorescent prot

33 ies (PWS) within the central 24 with 505 nm (cyan) and 625 nm (red) stimuli were evaluated in 50 indi

34 ities of coexpressed CFP-C-beta1CFP-N-gamma (cyan) and CFP-C-beta1YFP-N-gamma2 (yellow) complexes wer

35 a MAE of 4.64 dB for mesopic, 4.89 dB for DA cyan, and 4.40 dB for DA red testing in the absence of p

36 ing index has been achieved with red, green, cyan, and blue quantum dot light-emitting diodes as prim

37 orescent proteins to generate green, yellow, cyan, and red reporters, paving the way for multiplex pr

38 orrelation allowed prediction of mesopic, DA cyan, and red sensitivity with high accuracy (cross-vali

39 Cyan- and blue-elicited fluorescence have different sens

40 let], [green/yellow], [blue], [orange], and [cyan], appearing in this order, is recovered, featuring

41 binding between N@C-dots and IC resulted in cyan blue and quenching of N@C-dots fluorescence.

42 stability of this previously uncharacterized cyan blue anthocyanin-based colorant.

43 Finding a natural cyan blue dye equivalent to FD&C Blue No.

44 colors in nature's food palette-especially a cyan blue-giving scientists few sources for natural blue

45 In summary, red-green (or red-cyan) cells, along with blue-yellow and black-white cell

46 orter, NKCC1, we tagged the transporter with cyan (CFP) and yellow (YFP) fluorescent proteins and mea

47 ion of NKCC1, we tagged the transporter with cyan (CFP) and yellow (YFP) fluorescent proteins at two

48 Cyan (CFP) and yellow (YFP) fluorescent proteins were us

49 iving cells, these proteins were tagged with cyan (CFP) and yellow (YFP) mutants of the green fluores

50 Yellow (YFP) and cyan (CFP) fluorescent proteins were linked to the NH(2)

51 This protein is a member of the cyan class of Anthozoa FPs and exhibits broad, double-hu

52 rise to green fluorescence as opposed to the cyan color of emission that is characteristic for the ne

53 transfer (FRET) acceptor protein, emitting a cyan-colored fluorescence with an unusually long excited

54 se reflectance circular dichroism (DRCD) and cyan CPL signals, showing an intrinsic luminescence asym

55 s expressing 5-HT(2C) receptors labeled with cyan (donor) and yellow (acceptor) fluorescent proteins.

56 of spectrally distinct GFPs such as blue or cyan donors in combination with green or yellow acceptor

57 e transcription and the indirect coupling of Cyan dyes.

58 The four-state (orange, pear, green, and cyan) electrochromism demonstrated by the TAPA-PDA (ec)C

59 The second property is the bright cyan emission from the macromolecular product in its agg

60 s with a 15 to 30% increase in the yellow-to-cyan emission ratio because of a phosphorylation-depende

61 e fluorescent proteins, increasing yellow to cyan emission ratios by 10-30%.

62 o gain insight into the structural basis for cyan emission, the crystal structure of amFP486 (lambda(

63 es 20-35% changes in the ratios of yellow to cyan emissions because of phosphorylation-induced change

64 se 25-50% changes in the ratios of yellow to cyan emissions in live cells caused by phosphorylation-i

65 G-protein subunit beta 1 (YFP-beta 1) and a cyan-emitting GFP mutant fused to the N-terminus of the

66 e to decay to 90% of its initial value) of a cyan-emitting Ir-complex device is achieved compared wit

67 eon' (Ycam2) - comprising a fusion between a cyan-emitting mutant of the green fluorescent protein (G

68 They consist of tandem fusions of a blue- or cyan-emitting mutant of the green fluorescent protein (G

69 izes a newly developed FRET donor, monomeric cyan-excitable red fluorescent protein (mCyRFP1), which

70 ed combinatorial multi-site mutagenesis on a cyan-excitable red fluorescent protein to create the bri

71 re acquired including mesopic, DA red and DA cyan FCP, spectral-domain optical coherence tomography a

72 ssion with green fluorescence (cis-keto) and cyan fluorescence (excimer), an exceptional phenomenon t

73 In solution, the receptor shows cyan fluorescence (lambda(max)(em) = 485 nm, Phi(F) = 33

74 shows an increase in the ratio of yellow to cyan fluorescence emission by OST1/SnRK2.6-mediated phos

75 in locus control region driving the enhanced cyan fluorescence protein (ECFP) gene.

76 three positive control constructs in which a cyan fluorescence protein and a yellow fluorescence prot

77 cence protein-tagged RGS7.Gbeta5 complex and cyan fluorescence protein-tagged Galphaq, indicating a d

78 inetics of one representative of this class (cyan fluorescence protein/yellow fluorescent protein-flu

79 izes the Franck-Condon state, resulting in a cyan fluorescence, while the zwitterionic tautomer fluor

80 protein (GFP) towards the novel phenotype of cyan fluorescence.

81 GFP expression facilitates the evolution of cyan fluorescence.

82 energy transfer suggests that GAT1-YFP8 and cyan fluorescent (CFP) tagged ezrin (ezrin-CFP) exist wi

83 These mice exhibit cyan fluorescent cells specifically in the erythroid com

84 Finally, C-terminal yellow and cyan fluorescent fusion proteins, AT1R-YFP and BK-CFP, d

85 ts of yellow fluorescent protein (Venus) and cyan fluorescent protein (Cerulean) flank either the ent

86 reticulum Ca2+-ATPase (SERCA) were fused to cyan fluorescent protein (CFP) and coexpressed with PLB

87 maging to detect the proximity between CXCR1-cyan fluorescent protein (CFP) and fluorescence probes t

88 n a pixel-by-pixel basis using EGFR fused to cyan fluorescent protein (CFP) and Grb2 fused to yellow

89 To study this interaction, cyan fluorescent protein (CFP) and yellow fluorescent pr

90 r resonance energy transfer (FRET) pair, the cyan fluorescent protein (CFP) and yellow fluorescent pr

91 FP-APP-YFP [containing the fluorescent tags, cyan fluorescent protein (CFP) and yellow fluorescent pr

92 The MetN was sandwiched between cyan fluorescent protein (CFP) and yellow fluorescent pr

93 sfer (FRET) pairs with distinct spectra: (a) cyan fluorescent protein (CFP) and yellow FP (YFP), and

94 nsfer (FRET) of beta1a subunits labeled with cyan fluorescent protein (CFP) and/or yellow fluorescent

95 The methodology uses the cyan fluorescent protein (CFP) as a biomass indicator an

96 When tPA was imaged simultaneously with cyan fluorescent protein (CFP) as a cytosolic marker, th

97 odel cell system and the standard FRET pair, cyan fluorescent protein (CFP) as the donor and yellow f

98 length Kir6.2 subunits were linked to YFP or cyan fluorescent protein (CFP) at N or C termini, and al

99 nalysis of the subcellular localization of a cyan fluorescent protein (CFP) fusion and a protein-prot

100 ellow fluorescent protein (YFP) and enhanced cyan fluorescent protein (CFP) genes in which recombinat

101 Co-expression of Wld protein and cyan fluorescent protein (CFP) in axons and neuromuscula

102 alphas-CFP, with cyan fluorescent protein (CFP) inserted into an internal

103 epithelial (LLCPK) cells expressing stathmin-cyan fluorescent protein (CFP) or injected with stathmin

104 Mice that expressed cyan fluorescent protein (CFP) or yellow fluorescent pro

105 ignalling (RGS4) proteins were each fused to cyan fluorescent protein (CFP) or yellow fluorescent pro

106 by two nonfluorescent fragments (N and C) of cyan fluorescent protein (CFP) or yellow fluorescent pro

107 of Grb2, Shc, H-Ras, and K-Ras with enhanced cyan fluorescent protein (CFP) or yellow fluorescent pro

108 -length and truncated forms of VacA fused to cyan fluorescent protein (CFP) or yellow fluorescent pro

109 with various vector combinations to express cyan fluorescent protein (CFP) or YFP fused to either bi

110 Fusions of cyan fluorescent protein (CFP) to MldA, MldB, and MldC r

111 otein of 25 kDa (SNAP-25), were used to link cyan fluorescent protein (CFP) to yellow fluorescent pro

112 nal ribosome entry sequence (IRES)-dependent cyan fluorescent protein (CFP) translation were monitore

113 Mice expressing cyan fluorescent protein (CFP) under control of the Thy-

114 strain was used, containing a construct with cyan fluorescent protein (CFP) under Thy-1 promoter cont

115 otein (YFP) was fused to the N terminus, and cyan fluorescent protein (CFP) was fused to the C termin

116 Similarly, in the SLN-CFP reporter, Cyan Fluorescent Protein (CFP) was integrated downstream

117 xtended with a transmembrane (TM) domain and cyan fluorescent protein (CFP) were immobilized in the p

118 The reporters consist of fusions of cyan fluorescent protein (CFP), a phosphotyrosine bindin

119 variants of green fluorescent protein (GFP), cyan fluorescent protein (CFP), and yellow fluorescent p

120 ROSA(tdTom), tryptophan hydroxylase 1 (Tph1)-cyan fluorescent protein (CFP), c-Kit(wsh/wsh), and Neur

121 ensor is composed of an end-to-end fusion of cyan fluorescent protein (CFP), chicken metallothionein

122 lly confirmed by measurements on mixtures of cyan fluorescent protein (CFP), citrine ((Cit) a yellow

123 icroscopic measurements of fluorescence from cyan fluorescent protein (CFP), citrine, and linked CFP-

124 Upon excitation of the cyan fluorescent protein (CFP), emission intensities of

125 ter resonance energy transfer (FRET) between cyan fluorescent protein (CFP)- and yellow fluorescent p

126 nance energy transmission (FRET) analysis of cyan fluorescent protein (CFP)-arm-CTD-yellow fluorescen

127 raction between MacMARCKS and dynamitin with cyan fluorescent protein (CFP)-conjugated dynamitin as t

128 RBPMS immunoreactivity is localized to cyan fluorescent protein (CFP)-fluorescent RGCs in the B

129 3)-AChR-yellow fluorescent protein (YFP) and cyan fluorescent protein (CFP)-Ggamma(2).

130 Transfection of C8PA cells with cyan fluorescent protein (CFP)-HSL, yellow fluorescent p

131 Finally, the level and rate of recovery of cyan fluorescent protein (CFP)-M1-5 were lower than thos

132 Here, using cyan fluorescent protein (CFP)-tagged Fpn in conjunction

133 A functional cyan fluorescent protein (CFP)-tagged lac repressor-ER c

134 Cyan fluorescent protein (CFP)-tagged McpA, a stationary

135 performed following transient expression of cyan fluorescent protein (CFP)-tagged proteins and incub

136 ells, human DAT was fused to yellow (YFP) or cyan fluorescent protein (CFP).

137 -yellow fluorescent protein (YFP) and calnuc-cyan fluorescent protein (CFP).

138 tabilized by insertion into a loop in a host cyan fluorescent protein (CFP).

139 (FRET) between fusion proteins labeled with cyan fluorescent protein (donor) and yellow fluorescent

140 c mice expressing a synaptotagmin 1-enhanced cyan fluorescent protein (ECFP) fusion protein under con

141 llow fluorescent protein (EYFP) and enhanced cyan fluorescent protein (ECFP) variants of green fluore

142 id carrying the gene coding for the enhanced cyan fluorescent protein (ECFP) was also introduced into

143 protein (EYFP), Ht31 was linked to enhanced cyan fluorescent protein (ECFP), and these constructs we

144 rescent protein (GFP), a variant of enhanced cyan fluorescent protein (ECFP), has been determined to

145 yellow fluorescent protein (EYFP) > enhanced cyan fluorescent protein (ECFP), while a GST construct t

146 anced green fluorescent protein- or enhanced cyan fluorescent protein (ECFP)-tagged phospholipase Cde

147 ession of keratocan promoter-driven enhanced cyan fluorescent protein (ECFP).

148 Blue Fluorescent Protein (EBFP) and Enhanced Cyan Fluorescent Protein (ECFP).

149 Two PM markers, the enhanced cyan fluorescent protein (ECFP-Mem) and 3'-dioctadecylox

150 that contained enhanced yellow and enhanced cyan fluorescent protein (EYFP and ECFP, respectively) l

151 ion of tetanus toxin light chain tagged with cyan fluorescent protein (TNTCFP).

152 A recently engineered mutant of cyan fluorescent protein (WasCFP) that exhibits pH-depen

153 protein-Dictyostelium myosin II motor domain-cyan fluorescent protein (YFP-myosin-CFP) and compared t

154 otransfected with a mitochondrially targeted cyan fluorescent protein and an enhanced yellow fluoresc

155 onstrated by podocyte specific expression of cyan fluorescent protein and by electron microscopy.

156 red the interaction between DDR1 tagged with cyan fluorescent protein and DDR1 tagged with yellow flu

157 Fluorescent proteins enhanced cyan fluorescent protein and enhanced yellow fluorescent

158 ged the TAP1 and TAP2 subunits with enhanced cyan fluorescent protein and enhanced yellow fluorescent

159 Enhanced cyan fluorescent protein and enhanced yellow fluorescent

160 our method, we targeted QDs to cell surface cyan fluorescent protein and epidermal growth factor rec

161 human embryonic kidney 293T cells using H1R-cyan fluorescent protein and H2R-yellow fluorescent prot

162 Dual expression of SNAP-25 tagged with cyan fluorescent protein and VAMP-2 tagged with yellow f

163 omain of InsP3 receptors (types 1-3) between cyan fluorescent protein and yellow fluorescent protein

164 ing VP22 and VP13/14 as fusion proteins with cyan fluorescent protein and yellow fluorescent protein,

165 ding the human CrkII1-236 sandwiched between cyan fluorescent protein and yellow fluorescent protein,

166 tes inserted into a linker region separating cyan fluorescent protein and yellow fluorescent protein.

167 ubunits were genetically fused with enhanced cyan fluorescent protein and/or enhanced yellow fluoresc

168 s luciferase, yellow fluorescent protein, or cyan fluorescent protein at the carboxyl terminus of VPA

169 uced intracellular redistribution of an EGFR-cyan fluorescent protein chimera was markedly reduced by

170 Using ACE-fused cyan fluorescent protein donor and B2-fused yellow fluor

171 c for XOPS-mCFP, a membrane-targeted form of cyan fluorescent protein driven by the Xenopus rhodopsin

172 assays in plants that constitutively express cyan fluorescent protein fused to histone 2B provides en

173 an be rescued by overexpression of the PEX12-cyan fluorescent protein fusion protein, which targets t

174 oxisomes, as demonstrated for endogenous and cyan fluorescent protein fusion proteins by fluorescence

175 idate processing enzymes, which localized as cyan fluorescent protein fusions to mucocysts.

176 The advantage over previous constructs using cyan fluorescent protein is that our construct can be us

177 nally, chimeric proteins containing enhanced cyan fluorescent protein linked to wild-type CREB or CRE

178 fluorescent protein (YFP) and CD44 fused to cyan fluorescent protein on K562 cells.

179 s were addressed by tagging tapasin with the cyan fluorescent protein or yellow fluorescent protein (

180 ent colocalization of Akt2 fused with either cyan fluorescent protein or yellow fluorescent protein t

181 E12, E47, E12(NLS), or MyoD(NLS) and either cyan fluorescent protein or yellow fluorescent protein,

182 gion was used to introduce green, yellow and cyan fluorescent protein reporters into B. burgdorferi.

183 Using RD114-MFGS encoding cyan fluorescent protein to allow similar studies of nor

184 een genetically attached enhanced yellow and cyan fluorescent protein to the N or C terminus of the c

185 gitudinal retinal imaging of mice expressing cyan fluorescent protein under control of the Thy-1 prom

186 The retina of mice expressing cyan fluorescent protein under control of the Thy-1 prom

187 t the Trp66 position in the chromophore of a cyan fluorescent protein variant (CFP6) to investigate t

188 used to either yellow fluorescent protein or cyan fluorescent protein we can observe tau fusion prote

189 cell lines stably coexpressing PML-enhanced cyan fluorescent protein with other individual marker pr

190 f Escherichia coli K12 was flanked with CFP (cyan fluorescent protein) and YFP (yellow fluorescent pr

191 and double label (yellow fluorescent protein/cyan fluorescent protein) fluorescence labeling experime

192 e dynamic range and a 10% increase in donor (cyan fluorescent protein) fluorescence upon bleach of ye

193 almodulin, and the FRET donor ECFP (enhanced cyan fluorescent protein) into eNOS at a site adjacent t

194 a fluorescently tagged P-glycoprotein (MDR1-cyan fluorescent protein) permitted the drug-resistant p

195 in cells expressing the fusion protein CFP (cyan fluorescent protein)-dynamitin or CFP-MB (the MacMA

196 tein kinase A (PKA) consisting of fusions of cyan fluorescent protein, a phosphoamino acid binding do

197 nced yellow fluorescent protein and enhanced cyan fluorescent protein, allowing detection of zinc-ind

198 ore, the septin Cdc12p, fused with yellow or cyan fluorescent protein, also colocalized with Myo1p an

199 he unresolved amino-terminus and cerulean, a cyan fluorescent protein, as a tag at the carboxyl-termi

200 on of calmodulin within Citrine or fusion of cyan fluorescent protein, calmodulin, a calmodulin-bindi

201 ed from phagocytic cups earlier than did p85-cyan fluorescent protein, indicating that SHIP-1 inhibit

202 cts were used to express SNAP-25 tagged with cyan fluorescent protein, VAMP-2 tagged with yellow fluo

203 uorescence resonance energy transfer between cyan fluorescent protein- and yellow fluorescent protein

204 nce resonance energy transfer (FRET) between cyan fluorescent protein- and yellow fluorescent protein

205 e resonance energy transfer between enhanced cyan fluorescent protein-CaM and Na(V)1.5(4X) channels t

206 mouse liver sections after co-expression of cyan fluorescent protein-CCRP and yellow fluorescent pro

207 Selective immobilization of cyan fluorescent protein-D2 receptors (C-D2Rs) in the pl

208 refrontal cortex (PFC) neurons from enhanced cyan fluorescent protein-expressing mice.

209 uorescence resonance energy transfer between cyan fluorescent protein-fused and yellow fluorescent pr

210 tween Gialpha-yellow fluorescent protein and cyan fluorescent protein-Gbeta chimeras in HeLa cells.

211 al microscopy of coexpressed YFP-hGRbeta and cyan fluorescent protein-hGRalpha in COS-1 cells indicat

212 ne the stability of complexes formed between cyan fluorescent protein-labeled alpha(2A)-adrenorecepto

213 fluorescent protein (YFP) move along tubulin-cyan fluorescent protein-labeled microtubules in respons

214 The targeting of these enhanced cyan fluorescent protein-lac repressor-tagged RARalpha-c

215 We show that an enhanced cyan fluorescent protein-M. tuberculosis CrgA (ECFP-CrgA

216 Enhanced cyan fluorescent protein-Munc18-1 and a citrine variant

217 In addition, enhanced cyan fluorescent protein-Munc18-1 and a citrine variant

218 low fluorescent protein (EYFP)- and enhanced cyan fluorescent protein-NHPX fusions, we show here that

219 FRET between cyan fluorescent protein-PLB and yellow fluorescent prot

220 ciation with SERCA, measured by FRET between cyan fluorescent protein-SERCA and yellow fluorescent pr

221 escent protein-tagged (EYFP) GluCl alpha and cyan fluorescent protein-tagged (ECFP) GluCl beta.

222 sonance energy transfer was detected between cyan fluorescent protein-tagged DAT and yellow fluoresce

223 The cyan fluorescent protein-tagged Galpha and yellow fluore

224 Co-expression of hemagglutinin-tagged and cyan fluorescent protein-tagged UGT1A proteins, followed

225 an acetyl H3K9-specific scFv, tethered to a cyan fluorescent protein.

226 escent protein with the chloride-insensitive cyan fluorescent protein.

227 tro assays and cells overexpressing stathmin-cyan fluorescent protein.

228 nsgenic mice in which red, green, yellow, or cyan fluorescent proteins (together termed XFPs) were se

229 his upregulation, we incorporated yellow and cyan fluorescent proteins (YFPs and CFPs) into the alpha

230 icistronic mRNAs encoding enhanced green and cyan fluorescent proteins as the first and second cistro

231 ergy transfer (FRET) acceptor for the newest cyan fluorescent proteins.

232 was generated in transgenic mice carrying a cyan fluorescent reporter protein (CFP) gene linked to t

233 The crystal structure of the cyan-fluorescent Cerulean green fluorescent protein (GFP

234 thesis, cDNA constructs were created to fuse cyan-fluorescent protein (CFP) to the N terminus of SERC

235 outer membrane protein A (OmpA) fused to the cyan-fluorescent protein AmCyan.

236 us 2 (rAAV2) vectors encoding CIP fused with cyan-fluorescent-protein (CFP), with or without nuclear

237 Transplantation of cyan-fluorescent-protein-expressing haematopoietic stem

238 ration, the spectra featured broad emission (cyan for Ce(3+)) or sharp 4f-4f emission peaks (red for

239 ); cyan-green and red for Pr(3+); yellow and cyan for Dy(3+)) which can be fine-tuned to a wider gamu

240 the reversible intermolecular association of cyan-GFP-labelled calmodulin with yellow-GFP-labelled M1

241 The blue or cyan GFPs have the disadvantages of less brightness and

242 Thus, the afterglow emission (blue, cyan, green, and orange) of various CDAMs can be activat

243 lines expressing the B-glucuronidase (GUS), cyan, green, and yellow fluorescent proteins under contr

244 responsive to excitation light used to image cyan, green, or red fluorescent protein variants, allowi

245 ted by endogenous biomolecules compared with cyan, green, yellow, and orange FPs.

246 ur spectrally distinct fluorescent proteins (cyan, green, yellow, and red) that are fused to a transc

247 grouped into four color classes by emission, cyan, green, yellow, and red.

248 of GECIs in multiple colour channels (blue, cyan, green, yellow, red, far-red) and highlight areas f

249 ion peaks (red for Ho(3+); green for Tb(3+); cyan-green and red for Pr(3+); yellow and cyan for Dy(3+

250 a sharp detection border was present in the cyan/green spectral region.

251 o these technologies collectively as Dynamic Cyan Induction by Functional Integrated Receptors, or DC

252 P538-K66M suggest that natural selection for cyan is an exquisitely fine-tuned and highly cooperative

253 ission, with fluorescence colors tuning from cyan (lambda(em) = 470 nm) to red (lambda(em) = 652 nm)

254 are red shifted to 455 and 460 nm, emitting cyan light and green light, respectively.

255 meric protein, pdDronpa, that dissociates in cyan light and reassociates in violet light.

256 gineered, orange-red FP that is excitable by cyan light.

257 properties, we develop a highly dynamic CMY (cyan-magenta-yellow) palette ideal for entity encryption

258 lution for automated scoring of affinity and cyan-magenta-yellow-key (CMYK) color-coding for scoring

259 o express and compare six FPs (blue mTagBFP, cyan mCerulean, green CrGFP, yellow Venus, orange tdToma

260 nutes [3.22; 5.36], P < .001), and marked DA cyan mean sensitivity loss (-11.80 dB [-3.47; -19.85]),

261 Fluorescence was excited with cyan or blue LEDs on alternating camera frames, thus pro

262 cells as chimeric proteins fused to enhanced cyan or yellow fluorescent protein (CFP or YFP, respecti

263 FtsZ, FtsA, FtsQ, FtsL and FtsI to enhanced cyan or yellow fluorescent protein (ECFP or EYFP respect

264 f functional Ctr1 monomers fused with either cyan or yellow fluorescent protein resulted in fluoresce

265 receptors and G protein subunits tagged with cyan or yellow fluorescent protein showed that receptors

266 uorescence resonance energy transfer between cyan or yellow fluorescent protein-labeled G protein sub

267 Coexpression of receptors tagged with the cyan or yellow fluorescent proteins (CFP or YFP) resulte

268 HEK293 cells coexpressing IL-17RA fused to cyan or yellow fluorescent proteins (CFP or YFP) were us

269 genes corresponding to the N termini of the cyan or yellow fluorescent proteins were fused to the en

270 alpha(1C)- and beta-subunits were fused with cyan or yellow fluorescent proteins, and functionally co

271 eceptor constructs tagged with luciferase or cyan or yellow fluorescent proteins.

272 AL do not exhibit fluorescence in the green, cyan, or yellow emission channels, allowing the transgen

273 nds, including those that humans perceive as cyan, orange, and red.

274 opsin1 and found that it absorbs in the blue-cyan range of the light spectrum.

275 olouration efficiency at the band edge (blue-cyan region) are 4.8x10(6) m(-1) and 190 cm(2) C(-1), re

276 from the genome and expression of yellow or cyan reporters is enabled.

277 with differential degrees of mesopic and DA cyan sensitivity loss outside of the GA lesions.

278 mera of native PKCdelta fused to yellow- and cyan-shifted green fluorescent protein, which can be exp

279 and test various fluorescent dyes, spanning cyan to far-red wavelengths, for labeling performance in

280 bsorption bands at the 250-450 nm region and cyan to green emission properties.

281 nescence and wider color palettes within the cyan to green regions (Ce(3+)-Tb(3+)) and cool to warm w

282 broad range of emission maxima spanning from cyan to red.

283 y transfer (FRET) and increased the ratio of cyan to yellow emissions by up to 1.5-fold with apparent

284 f PSmOrange enable its simultaneous use with cyan-to-green photoswitchable proteins to study four int

285 MP decreased FRET and increased the ratio of cyan-to-yellow emissions by 10-30% in living mammalian c

286 The open fractures (vug) are colored cyan whereas the calcite-filled fractures (high density

287 sses between the fluorescent labels, such as cyan, yellow and monomeric red fluorescent proteins.

288 xed imaging of live human cells coexpressing cyan, yellow and red ATOM sensors detected biosensor tar

289 different fluorescent proteins (FP) (green, cyan, yellow or red FPs) in two different binary plasmid

290 final colors of the method (white, magenta, cyan, yellow, red, green, blue, colorless/gray, and blac

291 es, and arrival at the plasma membrane using cyan/yellow fluorescent protein-tagged glycosylphosphati

292 PRV-263 genome and conditional expression of cyan/yellow reporters.