ライフサイエンスコーパス: fluorescent protein

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

2 infected with M. bovis BCG expressing green fluorescent protein.

3 canonical amino acids into superfolder green fluorescent protein.

4 equences or the entire Ras proteins to Venus fluorescent protein.

5 first herpesvirus proteins to be fused to a fluorescent protein.

6 DCV-associated neuropeptide Y tagged with a fluorescent protein.

7 s of membrane proteins tagged with the mEos2 fluorescent protein.

8 of the OR-IRES-marker design coexpressing a fluorescent protein.

9 duct-specific lineage tracing marker yellow fluorescent protein.

10 ical work on photoinduced transformations in fluorescent proteins.

11 rtible labels, including genetically encoded fluorescent proteins.

12 issue containing transgenic or immunolabeled fluorescent proteins.

13 in the same cell by fusing them to different fluorescent proteins.

14 aging of transgenic quail embryos expressing fluorescent proteins.

15 uide RNA (sgRNA) scaffolds that bind sets of fluorescent proteins.

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

17 ally trapped silver nanoparticles and single fluorescent proteins.

18 redictions of maturation mechanisms in other fluorescent proteins.

19 ontaneous four-wave mixing in enhanced green fluorescent proteins.

20 ased on the use of the redox-sensitive green fluorescent protein 2, coupled to the glutaredoxin 1 (Gr

21 rol compared with the control enhanced green fluorescent protein AAV-DJ/8.

22 cells, with a concomitant decrease in green fluorescent protein abundance, and blocks primer extensi

23 d that an influenza virus encoding the Venus fluorescent protein acquired two mutations in its PB2 an

24 By inserting binding sites for fluorescent proteins adjacent to the rRNA operons and th

25 VP39 fused with three copies of the mCherry fluorescent protein also colocalized with microtubules.

26 The DII domain was fused to a yellow fluorescent protein and a nuclear localization sequence

27 (AHA2) that is translationally fused with a fluorescent protein and examined its cellular localizati

28 Green fluorescent protein and green fluorescent protein tagged

29 More particularly, using a series of novel fluorescent protein and lux operon reporter systems to d

30 e quantified translation initiation of green fluorescent protein and nanoluciferase in E. coli from a

31 sed imaging of constructs composed of only a fluorescent protein and the TM helices of Tar to demonst

32 on of dopamine through the generation of red fluorescent proteins and 6-decarboxylated betaxanthin pi

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

34 When combined with organelle-targeted fluorescent proteins and biosensors, we uncover previous

35 stabilized nanobodies can be used to deliver fluorescent proteins and enzymes to specific targets ins

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

37 opy (2PPM) to Galphai1 subunits labeled with fluorescent proteins and four GPCRs: the alpha2A-adrener

38 sparent and reliably preserves emission from fluorescent proteins and lipophilic dyes in membrane int

39 tags available, including both intrinsically fluorescent proteins and proteins that derive their fluo

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

41 teins (antibiotic resistance genes and Green Fluorescent Protein), and can be used to elucidate early

42 photo-highlighting using a photoconvertible fluorescent protein, and in combination with stimulated

43 Cyt b6f, and ATP synthase individually with fluorescent proteins, and revealed the heterogeneous dis

44 Many fluorescent proteins are currently available for biologi

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

46 Fluorescent proteins are used extensively for biological

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

48 docytic tracer atrial natriuretic factor-red fluorescent protein at early stages and nephrocyte loss

49 r AAV5-neutralizing antibodies using a green-fluorescent protein-based assay, and all 10 were enrolle

50 Fluorescent protein-based differentiation of isogenic st

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

52 Single-fluorescent protein biosensors (SFPBs) are an important

53 ors and expanded in vivo applications.Single fluorescent protein biosensors are susceptible to expres

54 enic fluorescent imaging, reported to reduce fluorescent protein bleaching rates, thereby increasing

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

56 ment of cells expressing nucleases linked to fluorescent proteins can be used to maximize knockout or

57 ion, we established a virus-free split-green fluorescent protein cell-cell fusion assay that enables

58 The methodology uses the cyan fluorescent protein (CFP) as a biomass indicator and the

59 various vector combinations to express cyan fluorescent protein (CFP) or YFP fused to either biologi

60 By targeting various dyes and fluorescent-protein chimeras to vesicles, the plasma mem

61 ered adeno-associated virus 9 carrying green fluorescent protein-CIP (AAV9-GFP-CIP) to brain cells vi

62 Interleukin 17A (IL-17A)-green fluorescent protein, cluster of differentiation 11c (CD1

63 or i-motif structures upstream of the green fluorescent protein-coding sequence markedly reduces the

64 In response to light, SFPS-RFP (red fluorescent protein) colocalizes with phyB-GFP in photob

65 ransgenic mice expressing a G85R SOD1-yellow fluorescent protein construct.

66 Here, we established a green to blue fluorescent protein conversion system to systematically

67 Green fluorescent protein costaining with alpha-smooth muscle

68 lin with C-peptide-bearing Superfolder Green Fluorescent Protein (CpepSfGFP) has been expressed in tr

69 ed by inserting a circularly permuted yellow fluorescent protein (cpYFP) into a region of the bacteri

70 oped by inserting circularly permuted yellow fluorescent protein (cpYFP) into the NADH-binding domain

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

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

73 nthetic Renilla luciferase and monomeric red fluorescent protein domains, as well as a truncated form

74 activity in living cells using destabilized fluorescent proteins (dsFPs).

75 orescent protein (GFP) and Discosoma sp. red fluorescent protein (DsRed) reporter genes driven by eit

76 293 cells overexpressing Discosoma spp. red fluorescent protein (DsRed)-tagged alpha1B-ARs and enhan

77 ations of in vitro mixtures of Enhanced Blue Fluorescent Protein (EBFP) and Enhanced Cyan Fluorescent

78 Fluorescent Protein (EBFP) and Enhanced Cyan Fluorescent Protein (ECFP).

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

80 -1-induced recruitment of DCC-enhanced green fluorescent protein (EGFP) from intracellular vesicles t

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

82 duce clustering of N-cadherin-enhanced green fluorescent protein (EGFP) on the plasma membrane of iso

83 sive clustering of N-cadherin-enhanced green fluorescent protein (EGFP) on the VSMC surface.

84 12 rAAV serotypes carrying an enhanced green fluorescent protein (EGFP) reporter gene in a panel of 1

85 sgenic mouse pre-labeled with enhanced green fluorescent protein (EGFP), whereas CN neurons were from

86 ge cells when inoculated with enhanced green fluorescent protein (EGFP)-expressing E. coli.

87 We used a strain with an enhanced green fluorescent protein (EGFP)-tagged transgene inserted nea

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

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

90 ing clearing capability, the preservation of fluorescent protein emission and membrane integrity and

91 functional vascular proteins, such as green fluorescent protein, enables expression in individual ce

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

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

94 level of expression that enables imaging of fluorescent-protein-expressing Bacteroides stably coloni

95 Combinatorial fluorescent protein expression in germline cells has pro

96 Here, we visualize telodendria via fluorescent protein expression in photoreceptor subtypes

97 r the first time on a protein from the green fluorescent protein family, showed a distribution of hyd

98 copy to demonstrate that these intrinsically fluorescent protein fibrils are permissive to proton tra

99 nuclear export signal (NES), as well as to a fluorescent protein for microscopy-based detection of it

100 system to screen reversibly photoswitchable fluorescent proteins for contrast and stability of rever

101 Genetically encoded fluorescent protein (FP)-based biosensor probes are usef

102 l for the quantitation of data obtained with fluorescent protein (FP)-based biosensors in vivo.

103 We used surface-modified fluorescent proteins (FPs) and determined their translat

104 Fluorescent proteins (FPs) engineered from bacterial phy

105 Self-complementing split fluorescent proteins (FPs) have been widely used for pro

106 isolation of native protein complexes.Split fluorescent proteins (FPs) have been widely used to visu

107 the visualization of individual cytoplasmic fluorescent proteins (FPs) in E. coli, allowing low-abun

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

109 Each tFT, composed of two fluorescent proteins (FPs) that differ in maturation kin

110 Several series of near-infrared (NIR) fluorescent proteins (FPs) were recently engineered from

111 play an important role in the photocycle of fluorescent proteins from the green fluorescent protein

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

113 Localization experiments using green fluorescent protein fusion constructs showed that, while

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

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

116 Microscopic analysis of a Mnx::yellow fluorescent protein fusion showed that the protein resid

117 In addition to the popular method of fluorescent protein fusion, live cell protein imaging ha

118 ression, transformation of P. infestans with fluorescent protein fusions and confocal microscopy to i

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

120 Fluorescent protein fusions to herpesvirus capsids have

121 Fluorescent protein fusions to the amino terminus of sma

122 Using fluorescent protein fusions, we have found that NAP1 [4]

123 structured and therefore may better tolerate fluorescent protein fusions.

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

125 ing beta-glucuronidase plus (GUSplus), green fluorescent protein (GFP) and Discosoma sp. red fluoresc

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

127 nock-in mice in which the pH-sensitive green fluorescent protein (GFP) and the Myc epitope were intro

128 M72 olfactory sensory neurons with the green fluorescent protein (GFP) as sensing components and obta

129 ribution and fluorescence intensity of green fluorescent protein (GFP) at different tumor depths duri

130 charged conjugated polymers (CPs) and green fluorescent protein (GFP) create a fluorescence resonanc

131 th type I pro-collagen promoter-driven green fluorescent protein (GFP) expression to identify fibrobl

132 cycle of fluorescent proteins from the green fluorescent protein (GFP) family.

133 nant pseudorabies viruses that encoded green fluorescent protein (GFP) fused in frame to the internal

134 is, by expressing the mutant form as a green fluorescent protein (GFP) fusion protein (VP1L138P-GFP)

135 Chromatin binding of p12-green fluorescent protein (GFP) fusion protein and functional

136 Green fluorescent protein (GFP) fusions are pervasively used t

137 Lv-BMP/GFP, containing human BMP-2 and green fluorescent protein (GFP) gene (BMP group); or (2) Lv-GF

138 boratory that had a single copy of the green fluorescent protein (GFP) gene integrated into its genom

139 g and EXT in Fos-GFP mice that express green fluorescent protein (GFP) in activated neurons (GFP+).

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

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

142 on of NR2B outside of LMAN or with the green fluorescent protein (GFP) in LMAN.

143 both an oncogene (ErbB2) and a floxed green fluorescent protein (GFP) in PR(Cre/+)mice, whose Cre ge

144 type and concentration dependence for green fluorescent protein (GFP) induction and both spatial and

145 Specifically, the rational design of green fluorescent protein (GFP) insertion into a ligand-bindin

146 We packaged an AAV genome encoding green fluorescent protein (GFP) into conventional AAV2 and exo

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

148 enty weeks after in vivo transduction, green fluorescent protein (GFP) marking in BM HSPCs (Lin(-)Sca

149 By generating synonymously variant green fluorescent protein (GFP) mRNAs with different potential

150 Using quantitative assays relying on green fluorescent protein (GFP) reporter genes, we found that

151 virus particles (RVPs) that package a green fluorescent protein (GFP) reporter-expressing West Nile

152 rated by site-directed mutagenesis and green fluorescent protein (GFP) tagging.

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

154 Green fluorescent protein (GFP) variants are widely used as ge

155 In line with these conclusions, even green fluorescent protein (GFP) was able to drive fission effi

156 Using an orthogonal Click reaction, Green Fluorescent Protein (GFP) was engineered to contain a ge

157 with different levels of expression of green fluorescent protein (GFP) were first mixed in a buffer s

158 mbine the fluorescence emission of the Green Fluorescent Protein (GFP) with the adhesion ability of t

159 tructures of two variants of truncated green fluorescent protein (GFP), i.e., split GFP with a beta-s

160 he 5-HT3a subunit drives expression of green fluorescent protein (GFP), we assessed the expression of

161 /TNFRSF6) 2Bck/J mice express enhanced green fluorescent protein (GFP), which enables in vivo correla

162 , which were engineered to express the green fluorescent protein (GFP)-based family of GECIs, GCaMP,

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

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

165 e performed high-throughput imaging of green fluorescent protein (GFP)-labeled proteasomes in the yea

166 gh throughput of 1 mL/min by capturing green fluorescent protein (GFP)-positive cells from blood.

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

168 aliana) differentially localize, using green fluorescent protein (GFP)-tagged proteins, to multiple a

169 ow that HEK293 cells stably expressing green fluorescent protein (GFP)-tagged wild-type La (GFP-La(WT

170 beta-arrestin-2, and internalized the Green Fluorescent Protein (GFP)-taggedbeta2 adrenoceptor at a

171 We found that BMP4/green fluorescent protein (GFP)-transduced MDSCs formed signif

172 ith bryophyte tissue and expression of green fluorescent protein (GFP)-UVR8 fusions in Nicotiana leav

173 and arabinose) into the production of green fluorescent protein (GFP).

174 lting in chromophore maturation in the green fluorescent protein (GFP).

175 with bone marrow from FVB/N-TgN [Tie2/green fluorescent protein (GFP)] 287 Sato mice.

176 S products, the commonly used standard green fluorescent protein (GFP, 27 kDa) and the polyketide syn

177 y of P. gingivalis-co-cultured GECs or green-fluorescent-protein (GFP)-P. gingivalis-NDK transfected

178 pression of a Gs-coupled DREADD (rM3Ds-green fluorescent protein [GFP], or "GsD").

179 Green fluorescent protein, GFP, has revolutionized biology, du

180 The availability of fluorescent proteins has facilitated the direct and real

181 However, while fluorescent proteins have been characterized for quantit

182 o provide an overview of the photophysics of fluorescent proteins, highlighting the interplay between

183 f cellulose synthase complexes tagged with a fluorescent protein; however, this approach has been use

184 was significantly impeded as shown by green fluorescent protein (ie, infected) cell quantification a

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

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

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

188 perturbation of hydration water around green fluorescent protein in solution.

189 c C57BL/6N(su9-DsRed2) mice that express red fluorescent protein in their mitochondria.

190 the properties of a diverse set of acceptor fluorescent proteins in combination with the optimized C

191 stochastically photoactivating and observing fluorescent proteins individually, there are no limitati

192 In cultured neurons, PDN1 fused to a fluorescent protein inhibited neurite outgrowth, an effe

193 ers for luciferase and a near-infrared (NIR) fluorescent protein (iRFP670), with the latter fused to

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

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

196 table inside the cells and when fused with a fluorescent protein label, the constitutively active G12

197 Scx green fluorescent protein-labeled (ScxGFP) reporter and Scx-kn

198 Live cell imaging of green fluorescent protein-labeled actin and talin shows that P

199 Using FRET between cerulean fluorescent protein-labeled Gbetagamma and the Alexa Flu

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

201 mouse model with cecal implantation of green fluorescent protein-labeled syngeneic colorectal cancer

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

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

204 gitudinally using transgenic mice expressing fluorescent proteins localized either in cytosol or in m

205 n this work we show that the widely used red fluorescent protein mCherry can be brought to a purely c

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

207 Among the orange and red fluorescent proteins, mCherry and mScarlet-I are the bes

208 recent development of transgenic mGLU-yellow fluorescent protein mice that express a genetic reporter

209 hermore, WT bone marrow (from enhanced green fluorescent protein mice) transplantation in bone marrow

210 ned large arteries in live CX3CR1-GFP (green fluorescent protein) mice, we show that nonclassical mon

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

212 Fluorescence imaging of a red fluorescent protein (mStrawberry), co-expressed with UT-

213 mouse model that expresses the pH-dependent fluorescent protein mt-Keima in order to more readily as

214 ondrial exchanges of matrix-targeted soluble fluorescent proteins, mtDsRed and photoactivable mtPA-GF

215 ced fluorescence intensity seen in the green fluorescent protein mutant, BFPms1, which results from t

216 ) (n=9), but not BAG3(Met81) (n=10) or green fluorescent protein (n=5), improved ischemic limb blood

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

218 cruitment of neutrophils labeled with Ds-Red fluorescent protein of Tg(lysC:DsRed) zebrafish upon TDC

219 mpartments in synthetic tissues by turning a fluorescent protein on-and-off.

220 anscription factor that drives expression of fluorescent proteins, opsins, and other genetically enco

221 The fluorescent proteins optically identified the PR constru

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

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

224 tions; photoactivatable and photoconvertible fluorescent proteins (PAFPs) are used widely in superres

225 ge by NE results in dissociation of the FRET fluorescent protein pair and alteration of the fluoresce

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

227 enous copy of Pol IV to the photoactivatable fluorescent protein PAmCherry.

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

229 Using a pH-sensitive green fluorescent protein, pHluorin, tagged to the extracellul

230 Depending on the task at hand, fluorescent protein photochemistry is regarded either as

231 nsgenic tomato PS gene tagged with the green fluorescent protein (PS-GFP) using a shoot- or root-spec

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

233 Green fluorescent protein reporter cell lines driven by functi

234 A Wnt-green fluorescent protein reporter demonstrated dynamic change

235 phenol (pNP) and measured the response via a fluorescent protein reporter expressed from a PobR promo

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

237 pulp cultures derived from a series of green fluorescent protein reporter transgenic mice that displa

238 r cardiac fibroblasts, the Collagen1a1-green fluorescent protein reporter.

239 Histone H2B-green fluorescent protein retention revealed that superficial

240 ted states in the reversibly photoswitchable fluorescent protein rsEGFP2.

241 s performance has not been duplicated in red fluorescent protein scaffolds.

242 Here, we adapted split green fluorescent protein (split-GFP) to systematically locali

243 ses, fluorescent labeling with visible light fluorescent proteins such as GFP and RFP suffers from po

244 tepwise photobleaching of SpoIVFB fused to a fluorescent protein supported the notion that the enzyme

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

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

247 Green fluorescent protein and green fluorescent protein tagged mutant EIF2A were expressed f

248 logy beta-arrestin 2 assay, imaging of green fluorescent protein-tagged beta-arrestin 2, and PathHunt

249 Using total internal reflection microscopy, fluorescent protein-tagged PKCs, and signaling biosensor

250 cells.Primary VSMCs were infected with green fluorescent protein-tagged wild type or US28-deficient H

251 DsRed)-tagged alpha1B-ARs and enhanced green fluorescent protein--tagged Rab proteins, pharmacologica

252 A fluorescent protein-tagging study pointed to a peroxisom

253 the utility of linear donors by introducing fluorescent protein tags in human cells and mouse embryo

254 multiple hiPSC lines with monoallelic green fluorescent protein tags labeling 10 proteins representi

255 ery of replicating reoviruses carrying large fluorescent protein tags, researchers have been unable t

256 Full-length TAN1 fused to yellow fluorescent protein, TAN1-YFP, and several deletion cons

257 a pH-sensitive, dual-excitation ratiometric fluorescent protein that also exhibits resistance to lys

258 Here, we report a chemically controllable fluorescent protein that enables us to rapidly produce s

259 inspired by the red shift seen in the yellow fluorescent protein that results from pi-pi stacking and

260 Fluorescent proteins that also bind DNA molecules are us

261 are dependent on the characteristics of the fluorescent proteins that are employed.

262 that hERG1a and hERG1b subunits tagged with fluorescent proteins that are FRET pairs exhibit robust

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

264 was evolved from the extremely thermostable fluorescent proteins thermal green protein (TGP) and eCG

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

266 In PLQ, the substrate is fused with a fluorescent protein to facilitate quantitative detection

267 porter virus that stably expresses the Venus fluorescent protein to identify antigen-bearing cells ov

268 the light-triggered proton wire of the green fluorescent protein to study its ground-electronic-state

269 To tackle this problem, the fusions of fluorescent proteins to alpha-synuclein C-terminus are o

270 Here we use membrane-targeted fluorescent proteins to reveal the fine structure of mou

271 We discovered that adding fluorescent proteins to the C-terminus resulted in const

272 To this end, we engineered red or green fluorescent proteins to the N- or C-terminus of PR, resp

273 S2 or PP7 coat proteins fused with different fluorescent proteins to the target genomic loci.

274 rms, utilizing either small-molecule dyes or fluorescent proteins, to monitor proteins, RNA, DNA, sma

275 However, a recombinant EBOV expressing a fluorescent protein tolerated swapping of GP with counte

276 l3-mutant zebrafish (box) with Tg(rag2:green fluorescent protein) transgenic zebrafish revealed defec

277 ernary (1 x 2) Bcl-2 PPI analyses by imaging fluorescent protein translation from mRNA outputs.

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

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

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

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

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

283 Green fluorescent protein was used to stably label 2.5 x 10(5)

284 axis protein (HIM-3) with a photoconvertible fluorescent protein, we established a spatial reference

285 Using titin kinase and green fluorescent protein, we show that monovalent Strep-Tacti

286 rial-surface associated BTPC-enhanced yellow fluorescent protein when both fusion proteins were coexp

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

288 nscriptome of the host show no difference in fluorescent proteins while the metatranscriptome of the

289 We synthesized 1.6 mg of green fluorescent protein with an isotope-labeled tyrosine fro

290 s and encodes the expression of GFPuv (green fluorescent protein with maximal fluorescence when excit

291 or quantitatively characterizing mixtures of fluorescent proteins with a large spectral overlap.

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

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

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

295 ient superinfection by WSMV expressing green fluorescent protein (WSMV-GFP).

296 imeric mice were created with enhanced green fluorescent protein WT mice marrow to the IL10KO mice.

297 righter and more photostable variants of the fluorescent protein YFAST among 60,000 variants.

298 ow that a hybrid reaction centre (RC)/yellow fluorescent protein (YFP) complex accelerates photosynth

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

300 Yellow fluorescent protein (YFP) was present in >96% of hepatoc