ライフサイエンスコーパス: fluorescent

1 using the particles in that region to become fluorescent.

2 The water-soluble and fluorescent [60]fullerene derivative (C60-serPF) was des

3 subunit-selective inhibitors and dual-color fluorescent activity-based probes for studying two of th

4 In vivo tumor labeling with fluorescent agents may assist endoscopic and surgical gu

5 effects of the DAT inhibitor cocaine and its fluorescent analog JHC1-64 on the plasma membrane distri

6 tions, and a pair of mice was imaged using a fluorescent analog of (125)I-iodo-DPA-713, DPA-713-IRDye

7 Specificity tests reveal that BR scrambles fluorescent analogues of common phospholipids but does n

8 The development of simple fluorescent and colorimetric assays that enable point-of

9 different experimental mixtures composed of fluorescent and nonfluorescent endocrine disruptors were

10 Here we used fluorescent and pristine polystyrene microplastics (PS-M

11 Fluorescent and radiolabeled MSCs (1x10(6)) were injecte

12 light to the target, and the other to detect fluorescent and reflected light.

13 his behavior is in stark contrast to that of fluorescent antibody conjugates.

14 O) material and shows a strong near-infrared fluorescent at ambient pressure and room temperature.

15 Infusion of fluorescent beads 3 d before pFUS+MB revealed the infilt

16 ssay was developed that uses THP-1 cells and fluorescent beads covalently-coupled with the malarial a

17 Fluorescent beads were conjugated to the sample surface

18 Labeling with a fluorescent beta2AR ligand shows the receptors are highl

19 sed human breast tumors stained in vivo with fluorescent bevacizumab at microdose levels.

20 mia confirmed that HL-FeNPs could be used as fluorescent biomarker for Al(3+) in live whole organisms

21 th no phototoxicity and no photobleaching of fluorescent biomarkers.

22 Hence, this fluorescent bioprobe can be employed for QA detection in

23 ic methods for visualization and examined by fluorescent, brightfield, and electron microscopy.

24 Antibody fluorescent brightness is one of the key parameters that

25 urements of cytosolic ([Ca(2+) ]i ; with the fluorescent Ca(2+) indicator rhod-2) and intra-SR ([Ca(2

26 al osteocytes by using a genetically encoded fluorescent Ca(2+) indicator.

27 vitro mouse model with a dextran-conjugated fluorescent calcium indicator.

28 ransformed HeLa cell lines were created with fluorescent cargos (mCherry) for the importin alpha/beta

29 h to examine emergent behaviors that couples fluorescent cell tracking with data-driven models.

30 All tdTomato fluorescent cells expressed syntaxin 1A and GABA-immunor

31 TdTomato fluorescent cells in the INL and GCL contained VIP-immun

32 Using the fluorescent cholesterol analogue dehydroergosterol, we e

33 The fluorescent color of the aptamer-labeled EGFR can be swi

34 rived from pairs of co-registered volumetric fluorescent confocal laser scanning microscopy (CLSM) im

35 t either small amounts of particles or other fluorescent contaminants of zein were up taken by the ro

36 include the typically low concentrations of fluorescent contrast agents, and tissue motion.

37 These fluorescent core-shell nanoparticles act as landmarks an

38 ng a chemically-fixed HeLa cell labeled with fluorescent core-shell nanoparticles as a model system,

39 duction of [PSI (+)] shows the appearance of fluorescent cytoplasmic rings when the prion domain is f

40 approach utilizing timed pulses of multiple fluorescent D-amino acids, we illuminate dynamic changes

41 Fluorescent data show that Dorsal accumulates on the ven

42 Here we report fluorescent derivatives of the nonselective agent asenap

43 d plasmonic gold film, enabling quantitative fluorescent detection of anti-HDV antibody in small aliq

44 l barrier function was measured by uptake of fluorescent dextran.

45 ken litter contained a biologically reactive fluorescent DOM component, identified as the nonhumic, b

46 gP/pDNA polyplexes loaded with a hydrophobic fluorescent dye are retained in local neural tissue for

47 Finally, we demonstrate that the fluorescent dye cargo was able to penetrate intra-tumora

48 re generated, half of which were seeded with fluorescent dye for imaging purposes.

49 enhancement of parenchymal labeling with the fluorescent dye Hoechst 33342.

50 Here, we demonstrate a fluorescent dye method suitable for visualization of one

51 t labelling of viral particles with either a fluorescent dye or biotin.

52 ered between small atomic ions (current) and fluorescent dye permeants, indicating that these permean

53 ion of a small molecule-type thermosensitive fluorescent dye, ERthermAC, to monitor thermogenesis in

54 onfocal microscopy using a flavonol-specific fluorescent dye.

55 miluminescent precursor to a nearby emissive fluorescent dye.

56 Using the fluorescent-dye conjugate, [S14R, W50Pra(Bodipy)]Ts1, we

57 Organic fluorescent dyes ( approximately 4 nm), quantum dots, ei

58 an elevate the fluorescence signal of single fluorescent dyes by several orders of magnitude.

59 We find that >90% of AMPARs labeled with fluorescent dyes or sQDs were diffusing in confined nano

60 template using high-resolution melting (HRM) fluorescent dyes that intercalate into the growing duple

61 A large number of fluorescent dyes were loaded into Alb NPs to make Alb NP

62 GPCRs with biophysical probes, particularly fluorescent dyes, and highlight the relevant chemical bi

63 ifunctional smHSSs integrated with proteins, fluorescent dyes, quantum dots, and magnetic nanoparticl

64 ect, site-specific labeling of proteins with fluorescent-dyes in live cells.

65 rmed using reconstituted MscL in a liposomal fluorescent efflux assay.

66 ables the generation of a spatial pattern of fluorescent emission at the intersection of two structur

67 exibility and power of C-DSLM by quantifying fluorescent features in tissue from multiple animal mode

68 ogeochemistry, but its relationship with the fluorescent fraction of DOM (FDOM) remains poorly resolv

69 We expressed fluorescent fusions of FtsZ from diverse photosynthetic

70 l data show that a systemically administered fluorescent GLP-1R agonist accesses the LDTg and is juxt

71 stable astrocytes clones with an integrated fluorescent HIV reporter and Cas9 expression gene were g

72 Use of fluorescent HSV-1 virions demonstrated a pattern of vira

73 in a 96-well plate, from which multichannel fluorescent images are acquired with automated time-laps

74 bled tagging of cellular RNA, in addition to fluorescent imaging as well as enrichment of RNA in cell

75 an be simultaneously assessed through simple fluorescent imaging for each lineage reporter.

76 We used live-cell fluorescent imaging of intravirion fluid phase markers t

77 covalent decoration of intimin for live cell fluorescent imaging of the dynamics of the bacterial out

78 report an integrated channel waveguide-based fluorescent immunosensor with the ability to detect a ma

79 trivalent LAIV-vaccinated children using the fluorescent immunospot assay (FluoroSpot) with heterolog

80 EGFR CNG was determined by fluorescent in situ hybridization (FISH) using prespecif

81 roaches (allele-specific RNAseq, nascent RNA-fluorescent in situ hybridization and immunofluorescence

82 unohistochemistry for MYC and BCL2, and with fluorescent in situ hybridization for MYC, BCL2, and BCL

83 testes than in ovaries was also detected by fluorescent in situ hybridization in G. f.

84 Fluorescent in situ hybridization was performed to deter

85 We used fluorescent in situ hybridization with probes for nascen

86 ween e-liquids, (ii) that e-liquids are most fluorescent in the UV range (between 350 and 405 nm) and

87 canning microscopy of calcium dynamics using fluorescent indicators is a widely used imaging method f

88 Here, we present highly potent and selective fluorescent inhibitors that we show to be useful chemica

89 We constructed fluorescent InsB10-23:DQ8 tetramers, stained peripheral

90 s II, and 14.4% class I and class II at mean fluorescent intensity greater than 1000.

91 Under the optimum condition, the fluorescent intensity of the probe system linearly respo

92 Internally quenched fluorescent (IQF) peptide substrates originating from FR

93 V staining strategy, with the amine-reactive fluorescent label, 5-(and-6)-Carboxyfluorescein Diacetat

94 was probed simultaneously with only a single fluorescent label.

95 eal-time imaging in zebrafish displayed that fluorescent-labeled blood vessels showed enhanced intrat

96 s have created a pressing need for efficient fluorescent labeling procedures to visualize and detect

97 fortunately, this method inherently requires fluorescent labeling which has several drawbacks.

98 Uptake profile of fluorescent-labelled exosomes in epithelial cells was as

99 Such methods, however, usually rely on fluorescent labels for chemical targeting, which could p

100 ttle as 1 h without the use of antibodies or fluorescent labels of any kind.

101 sphate and Ca(2+), or by the identity of the fluorescent labels.

102 h high specificity that correlates well with fluorescent labels.

103 ring index (CRI) of 73 which is similar to a fluorescent light source and correlated color temperatur

104 tail conditions (4+/-0.5 degrees C, with 14h fluorescent light) for 9days.

105 ients with pathogenic mutations in VCP Using fluorescent live cell imaging and respiration analysis w

106 These highly fluorescent M2FA adducts may play important roles in hum

107 OX3097D-Bol olive fly carries a fluorescent marker (DsRed2) for identification and a sel

108 g were confirmed by cell genomic DNA PCR and fluorescent marker expression analysis.

109 sociated virus that drives the expression of fluorescent marker into the VTA of male mice that had Cr

110 Fluorescent marker proteins are expressed at high levels

111 We show that the photoacids can be used as fluorescent markers for following the progression of amy

112 volutionized researchers' ability to perform fluorescent measurements of molecules, cells, and struct

113 onic nanostructures has been demonstrated by fluorescent microarray immunoassay and LSPR measurements

114 n scan at 9 excitation wavelengths common to fluorescent microscopy and found (i) that autofluorescen

115 Here, we used electron and fluorescent microscopy and show that CLas induces the fo

116 trum of glomerular diseases characterized on fluorescent microscopy by C3 accumulation with absent, o

117 A fluorescent microsphere hybridization assay was designed

118 With this instrument format and fluorescent microsphere standards, we obtain analysis ra

119 tivation, followed by specific labeling with fluorescent moieties, we generated a novel class of FRET

120 Here we report the use of fluorescent molecular rotors in combination with Fluores

121 ates can be discriminated by a combinatorial fluorescent molecular sensor.

122 th DNA intercalated with ethidium bromide, a fluorescent molecule.

123 Movies of single fluorescent molecules allowed their movement through the

124 th the apparent diffusion coefficient of the fluorescent molecules.

125 nder well-defined concentrations of AMPs and fluorescent molecules.

126 We developed fluorescent, morphology-based seeding assays that allow

127 , photophysics, and biochemical utility of a fluorescent NAD(+) analogue based on an isothiazolo[4,3-

128 y excite either the monomeric species or the fluorescent nanoaggregates.

129 s study investigates such interactions using fluorescent nanodiamonds (FNDs) coated with vaccinia env

130 ssue clearing and a TAM-targeting injectable fluorescent nanoparticle (NP) to examine three-dimension

131 A biocompatible fluorescent nanoprobe for singlet oxygen ((1) O2 ) detec

132 In this work, we use a nonphotobleaching fluorescent nanosensor array based on single-walled carb

133 ingle-turnover incorporation kinetics of non-fluorescent native nucleotides by DNA polymerases.

134 the FRET-based calcium biosensor Twitch1 and fluorescent NFAT.

135 changes associated with channel gating, the fluorescent non-canonical amino acid coumarin-tyrosine w

136 ch-clamp fluorometry, and incorporation of a fluorescent noncanonical amino acid, we show that there

137 Herein we present a dual fluorescent-nuclear probe based on self-assembly of vanc

138 mtosecond illumination of rsEGFP2 in its non-fluorescent off state and observed their build-up (withi

139 typically a nonfluorescent "off" state and a fluorescent "on" state at well-defined coordinates on su

140 using light-activated DNA to encode either a fluorescent or a pore-forming protein.

141 eptor was synthesized and was processed into fluorescent organic nanoparticles (FONs) for determinati

142 Incorporation of the duplex fluorescent output [green and red fluorescence proteins]

143 substrate, which enabled us to image single fluorescent particles as small as 50 nm in diameter and

144 ly 2010s, the same method was used to define fluorescent patterns on QD films, allowing for further a

145 Trypanosoma brucei When added to cells, this fluorescent peptide is internalized within vesicular str

146 Fluorescent peptides are valuable tools for live-cell im

147 use in live-cell STED nanoscopy.Ratiometric fluorescent pH probes are useful tools to monitor acidif

148 Tagging of SipA with the small fluorescent phiLOV tag, which can pass through the type

149 operated PLCbeta1 activity measured with the fluorescent phosphatidylinositol 4,5-bisphosphate/inosit

150 ed coral systematically exhibited fragmented fluorescent pigments adjacent to the disease front as in

151 A novel and simple fluorescent platform based on (2,2'-((1E,1'E)-((6-bromop

152 (FE) in combination with a fibrosis-targeted fluorescent probe allows to visualize RIPF in real-time

153 ree-dimensional pseudopods we: (i) developed fluorescent probe combinations that distinguish cortical

154 MIP) was synthesized and used as a selective fluorescent probe for Metronidazole detection.

155 atively, our results suggest that this novel fluorescent probe is a powerful tool to understand FA ut

156 hput screening (HTS) was conducted using the fluorescent probe substrate ASP(+) in cells overexpressi

157 +)), a photo-induced electron transfer (PET) fluorescent probe system was developed to determine the

158 ynthesized as a colorimetric and ratiometric fluorescent probe that can be utilized to rapidly, sensi

159 pect to our previously reported indole-based fluorescent probe.

160 However, very few NIR-IIb fluorescent probes exist currently.

161 e transitions and increases the potential of fluorescent probes for applications in analytical chemis

162 th down-converting nanocrystals as promising fluorescent probes for in vivo imaging in this spectral

163 Fluorescent probes for signal generation were designed t

164 To construct more drug-like fluorescent probes suitable for imaging by confocal micr

165 Fluorescent probes that are able to directly measure vis

166 of foreign molecules such as functionalized fluorescent probes, antibodies, or plasmid DNA to living

167 hes involving aptamers, enzymes, DNA probes, fluorescent probes, interacting proteins and antibodies

168 pectral window; when combined with available fluorescent probes, this palette provides 24 resolvable

169 ilizes in situ supramolecular capture of the fluorescent product.

170 some medium by monitoring the development of fluorescent products formed by lipid oxidation.

171 roscopy methods are challenging, because the fluorescent properties of the imaging antibodies are hig

172 Using enhanced green fluorescent protein (EGFP) as a model protein, we carry

173 ns of rabies virus expressing enhanced green fluorescent protein (EGFP) into the dLGN.

174 e expressing the farnesylated enhanced green fluorescent protein (EGFPf) from the transient receptor

175 For instance, green fluorescent protein (GFP) and the cowpea chlorotic mottl

176 d-type and Fos-GFP mice, which express green fluorescent protein (GFP) in activated neurons, after ap

177 reened for the ability to esterify the green fluorescent protein (GFP) in an aqueous environment.

178 embryonic stem cells (ESCs) expressing green fluorescent protein (GFP) into diploid embryos.

179 In-frame fusion of green fluorescent protein (GFP) to the C-terminus of the chann

180 Green fluorescent protein (GFP)-expressing Escherichia coli wa

181 Heterozygous green fluorescent protein (GFP)-knock-in mice revealed rapid i

182 oughput screening based on reversal of green fluorescent protein (GFP)-reported, RNAi-mediated silenc

183 fector Pi04314, expressed as a monomeric red fluorescent protein (mRFP) fusion protein with a signal

184 genic P301L MAPT mutation labeled with green fluorescent protein (T40PL-GFP Tg mouse line) exhibited

185 Yellow fluorescent protein (YFP) is often used as an acceptor b

186 -acid NSs peptide or encoding enhanced green fluorescent protein [eGFP]) or an NSs-eGFP fusion protei

187 Here, we chose enhanced green fluorescent protein as a model system and subjected it t

188 y knocking down the gene expression of green fluorescent protein by 37% over 4 days.

189 erexpressing SLC30A9 fused to enhanced green fluorescent protein demonstrated vesicular cytosolic loc

190 Here Ast et al. describe a dual fluorescent protein design whereby a reference fluoresce

191 The C-terminal in-frame green fluorescent protein fusion may slow down the proteasome-

192 AtHEMN1-green fluorescent protein fusion protein was found targeted to

193 detection and in vivo localization of AtCPT7 fluorescent protein fusions showed that AtCPT7 resides i

194 Fluorescent protein fusions to the amino terminus of sma

195 structured and therefore may better tolerate fluorescent protein fusions.

196 experiments with a combination of promoters, fluorescent protein genes, and piggyBac transposase vect

197 he 335 base-pair gene that encodes the green fluorescent protein iLOV from ten functionalized oligonu

198 layers of biologically produced recombinant fluorescent protein in optical microcavities is demonstr

199 transgenic mice that express enhanced green fluorescent protein in PV+ INs.

200 uorescent protein design whereby a reference fluorescent protein is nested within a reporter fluoresc

201 anslational start codon and a membrane-bound fluorescent protein lacking its start codon.

202 ee different LGR5 isoforms along with unique fluorescent protein lineage reporters in the same mouse.

203 ted populations of E. tenella expressing the fluorescent protein mCherry, linked to endogenous signal

204 mes the challenge of spectral overlap in the fluorescent protein palette.

205 nts were assayed in an HIV-1-inducible green fluorescent protein reporter cell line.

206 IL-10 green fluorescent protein reporter mice revealed that regulato

207 Both (PR)50- and (GR)50-green fluorescent protein tagged dipeptides were present in th

208 orescent protein is nested within a reporter fluorescent protein to control for such artifacts while

209 ombinant reovirus S1 gene that expressed the fluorescent protein UnaG.

210 erns of a transgene construct encoding green fluorescent protein under the Ss-riok-2 promoter in post

211 by showing that folding of an enhanced green fluorescent protein variant designed computationally to

212 scopy showed that a fraction of HCF222-green fluorescent protein was detectable in the endoplasmic re

213 associated viruses encoding a control (green fluorescent protein) or 2 BAG3 (Bcl-2-associated athanog

214 We show using the gfp mRNA (encoding green fluorescent protein) that non-sRNAs can be engineered to

215 was disabled (mut-Ad3GFP, where GFP is green fluorescent protein).

216 which is a synthetic RNA mimic of the Green Fluorescent Protein, from its split segments.

217 rfusion compared with Met81- (n=25) or green fluorescent protein- (n=29) expressing animals.

218 therapeutics, we infected them with a green fluorescent protein-expressing MeV.

219 V-1 Tat into the lateral ventricle of yellow fluorescent protein-expressing transgenic mice produced

220 hy, we adoptively transferred enhanced green fluorescent protein-labeled monocytes into Dysf-deficien

221 In contrast to routine fluorescent-protein-based protein imaging, technology fo

222 The slow maturation time of fluorescent proteins (FPs) limits the temporal accuracy

223 Green-to-red photoconvertible fluorescent proteins (pcFPs) are powerful tools for supe

224 uestion by using transgenic Hydra expressing fluorescent proteins and a multiscale experimental and n

225 Here we develop methods for expression of fluorescent proteins and for gene deletion in a model pl

226 resent strategies to engineer BphP-based NIR fluorescent proteins and review their properties and app

227 vable resolution of optical imaging, but few fluorescent proteins are suitable for super-resolution m

228 However, while fluorescent proteins have been characterized for quantit

229 l systems genetically-targeted expression of fluorescent proteins is the method of choice; however, t

230 Plasmid constructs containing fluorescent proteins or targeted genes of Toxoplasma gon

231 multiple stable transgenic lines expressing fluorescent proteins under several tissue-specific promo

232 lar modeling to strategically place tags and fluorescent proteins within GSDMD that support native py

233 HIV, type 1 (HIV-1), which can generate free fluorescent proteins within the viral particle.

234 of entangled light in biologically produced fluorescent proteins would be promising because of their

235 nce in a set of virally encoded mutant green fluorescent proteins, which allowed us to measure the ra

236 that this approach can be extended to other fluorescent proteins.

237 ally trapped silver nanoparticles and single fluorescent proteins.

238 ical work on photoinduced transformations in fluorescent proteins.

239 aging of transgenic quail embryos expressing fluorescent proteins.

240 and invasion are demonstrated; near-infrared fluorescent psiRGDechi derivative is able to detect alph

241 cataract showed increasing concentration of fluorescent PTM towards the lens centre in accord with t

242 he synthetic creation of molecularly tunable fluorescent quantum defects in semiconducting single-wal

243 veral properties such as catalytic activity, fluorescent quencher and electrochemical, high surface a

244 vity and surface area to oxygen transfer and fluorescent quenching capabilities are also highlighted.

245 A new biocompatible fluorescent receptor 1 was synthesized by conjugating di

246 ment of a novel approach, a variant of FRAP (fluorescent recovery after photo-bleaching) modified to

247 ous murine model of melanoma incorporating a fluorescent reporter allele (tdTomatoLSL).

248 The expression of a protected fluorescent reporter and flux of a high-value metabolite

249 Fluorescent reporter fusions showed that SLI1 is confine

250 These changes were monitored using a novel fluorescent reporter gene, pMitoTimer, that allows asses

251 mber of disulfides were investigated using a fluorescent reporter system in order to optimize linker

252 nes; (3) simple knock-in of epitope tags and fluorescent reporters (e.g. Sox2-V5 and Sox2-mCherry); a

253 ternative (GlycoFRET), where terbium-labeled fluorescent reporters are irreversibly attached to recep

254 eostasis in proliferating human cells, using fluorescent reporters for AMPK activity, Akt activity, a

255 form that enables accurate quantification of fluorescent reporters in complex human iPSC-derived reti

256 Here, we used time-lapse microscopy and fluorescent reporters of DNA replication and chromosome

257 Here, we use behavioral assays and fluorescent reporters to show that axonal fusion enables

258 r simple screening assays with luciferase or fluorescent reporters.

259 ediated oxidation of Amplex Red (AR) to form fluorescent resorufin.

260 In the present study, we used fluorescent retrograde tracing to determine the olivary

261 es and tagged with environmentally sensitive fluorescent rhodamines [e.g., tetramethylrhodamine (TMR)

262 e properties make tC(O) a highly interesting fluorescent RNA base analogue for detailed FRET-based st

263 the ability to switch between plasmonic and fluorescent semiconductor nanocrystals might lead to the

264 t improvements in our abilities to introduce fluorescent sensors into cells, coupled with advances in

265 ed pH oscillations that could be imaged with fluorescent sensors.

266 up to 16 MS2 binding motifs to enable robust fluorescent signal amplification.

267 effects of PIT are monitored using the IR700 fluorescent signal based on macroscopic fluorescence ref

268 that the distribution of the radioactive and fluorescent signal colocalized with CEA-expressing tumor

269 Optical mapping is a technique for capturing fluorescent signal patterns of long DNA molecules (in th

270 mages showed that the intensity of the green fluorescent signal revealed much weaker signal from the

271 Preservation of fluorescent signal was achieved by decreasing clearing t

272 The fluorescent signal was then obtained through fluorescenc

273 e efficiency of excitation and collection of fluorescent signals in the presence of fluorophore photo

274 These two fluorescent SOFs exhibit intriguing and varied photophys

275 ut has been limited to low concentrations of fluorescent species and is only suitable for studying hi

276 namics at up to millimolar concentrations of fluorescent species.

277 ations, and photo-excitable photochromic and fluorescent species.

278 We apply microfluidic and fluorescent spectroscopy techniques to study the coordin

279 ecular complementation assay by assembling a fluorescent Spinach aptamer, which is a synthetic RNA mi

280 sue with subsequent immunohistochemistry and fluorescent staining of histological features.

281 he brains of AD-ANCL patients including auto-fluorescent storage material (AFSM) accumulation, CSPalp

282 oscopy and measuring luminal accumulation of fluorescent substrates, we assessed the transport activi

283 Two kinds of shape-controllable and fluorescent supramolecular organic frameworks (cuboid or

284 d and demonstrated the potential use of this fluorescent tag for in vivo tracking of individual effec

285 face wetting properties and conjugation with fluorescent tags are demonstrated to highlight the poten

286 chieved by labeling their reducing end using fluorescent tags.

287 e broadly applied to direct detection of any fluorescent target, including nucleic acids and proteins

288 ignificantly enhancing the delivery of 60nm fluorescent tracer BPN across the blood-tumor barrier in

289 is led to the development of 4 (TUG-1609), a fluorescent tracer for FFA2 with favorable spectroscopic

290 ome model combined with a promoter-specific, fluorescent translation reporter confirmed clusters are

291 ion calorimetry, and radio-ligand uptake and fluorescent transport assays on ZntB reconstituted into

292 ema pallidum particle agglutination [TP-PA], fluorescent treponemal antibody absorption [FTA-ABS] tes

293 ibe the development of a genetically encoded fluorescent tRNA fusion with the potential for imaging i

294 photolyze these molecules, only sunlight and fluorescent tubes will be important to room-averaged ind

295 Based on WR6, two NIR fluorescent turn-on probes, WSP-NIR and SeSP-NIR, were d

296 Using a fully functional fluorescent version of Arabidopsis thaliana FLA4 we show

297 Recent work has introduced a new fluorescent voltage sensor, ASAP1, which can monitor rap

298 e mice, we examined excitatory plasticity in fluorescent VTA GABA cells.

299 We found that injection of fluorescent wild-type SOD1 (wt SOD1YFP) or monomeric mut

300 The non-fluorescent YFP variant sREACh is an efficient acceptor,