ライフサイエンスコーパス: RFP

1 RFP expression was also shown by flow cytometry and repl

2 RFP expression was analyzed by flow cytometry and viral

3 RFP insertion marked putative pax8-lineage cells with fl

4 RFP is expressed in the dorsal spinal cord.

5 RFP sites are polar, stalling replication forks only whe

6 RFP was able to repress transcriptional activation by E4

7 RFP-FimXDeltaREC, unlike RFP-FimX, is no longer localize

8 RFP-GRalpha receptor behaves similarly to the wild-type

9 RFP-GRalpha translocation was temperature sensitive, occ

10 RFP-Luc-Sk-Hep-1 were implanted into NOD-scid mice liver

11 including PC-3-RFP prostate cancer, HCT-116-RFP colon cancer, MDA-MB-435-RFP breast cancer, and HT10

12 Using IL-17F-RFP together with a Foxp3 reporter, we found that the de

13 The AtSRC2.2-RFP fusion also colocalized with two proteins previously

14 MIA-PaCa-2-RFP pancreatic cancer cells were transduced with the Dis

15 g signal 1 and peroxisome targeting signal 2-RFP in transgenic Arabidopsis.

16 sing human cancer cell lines, including PC-3-RFP prostate cancer, HCT-116-RFP colon cancer, MDA-MB-43

17 cancer, HCT-116-RFP colon cancer, MDA-MB-435-RFP breast cancer, and HT1080-RFP fibrosarcoma were tran

18 ells and M2 cells transfected with filamin A-RFP), caveolin-1-GFP was concentrated in intracellular v

19 Sla1-GFP and Abp1-RFP lifetimes were accelerated in arp2-7 mutants, which

20 imaging of Sla1-GFP, a coat marker, and Abp1-RFP, which marks the later actin phase of endocytosis.

21 larization process in vitro by using an ActA-RFP (red fluorescent protein) fusion.

22 autophagy, neurons were infected with adeno-RFP-LC3 and subjected to trophic factor withdrawal, and

23 ferent patterns of gene expression: alphaSMA-RFP positive cells, collagen-EGFP positive cells, and ce

24 The alphaSMA-RFP mice were crossed with collagen-EGFP mice to generat

25 Emu-ret mice carrying an RFP/RET fusion gene under the transcriptional control of

26 h rabbit myocardium and in mice harboring an RFP-GFP-LC3 transgene.

27 reB, co-visualization of GFP-tagged DnaA and RFP-tagged MreB demonstrates that DnaA and MreB adopt di

28 is, histochemical GUS staining, and eGFP and RFP fluorescent microscopy.

29 conditions, nephrons expressed few EGFP and RFP puncta, but ischemia-reperfusion injury (IRI) led to

30 ete release of constituent proteins, GFP and RFP (mCherry), from a polyprotein precursor, in bacteria

31 el fluorescent proteins derived from GFP and RFP in an in vitro system that allows direct analysis of

32 cellular measurements, as shown for GFP and RFP in mammalian cells.

33 By revealing how GFP and RFP protein environments steer chemistry to favor fluoro

34 e light fluorescent proteins such as GFP and RFP suffers from poor tissue penetration and high backgr

35 d was produced in recombinant form (His- and RFP-tagged).

36 t recruitment of RFP approximately KLCR1 and RFP approximately CaM2 to microtubules.

37 The potential bias in RSN and RFP estimates were <5 and <20%, respectively.

38 and evaluated the potential bias of RSN and RFP estimates.

39 Interestingly, while GFP-Wdr68 and RFP-Dyrk1a co-localized to the cell nucleus as expected

40 actions and localization of Apc2-GFP and Apc-RFP to branch points suggests that these proteins work t

41 Transient overexpression of ARK1-RFP (red fluorescent protein) increased microtubule cata

42 ute [mRNA] concentration and the associated [RFP] expressed from an inducible plasmid.

43 an cells, and it outperforms other available RFPs with regard to photostability and phototoxicity.

44 h one of the following constructs: RCASBP(B)-RFP, RCASBP(B)-RFP-scrambled RNAi, or RCASBP(B)-RFP-GluA

45 , RCASBP(B)-RFP-scrambled RNAi, or RCASBP(B)-RFP-GluA2 RNAi.

46 llowing constructs: RCASBP(B)-RFP, RCASBP(B)-RFP-scrambled RNAi, or RCASBP(B)-RFP-GluA2 RNAi.

47 in the ND-GFP mice transplanted with B16F10-RFP.

48 ronment of the autolysosomes, whereas bright RFP signals remained.

49 that some Rim20-GFP foci correspond to Bro1-RFP foci, whereas others do not.

50 s having both Ure2p-GFP aggregates and Btn2p-RFP dots display striking colocalization.

51 ation of rKSHV.219 occurred, as evidenced by RFP expression, the expression of the late virion protei

52 Transcriptional repression by RFP was trichostatin A sensitive and did not involve an

53 nt protein (EGFP; pKa 5.9), we generated CAG-RFP-EGFP-LC3 mice to distinguish early autophagic vacuol

54 t deprivation, renal epithelial cells in CAG-RFP-EGFP-LC3 mice produce autophagic vacuoles expressing

55 C57BL/6J, Ccr2(RFP/+)Cx3cr1(GFP/+), Ikk(F/F) mice and LysM-Cre/Ikk(F/F)

56 Using CX3CR1(GFP/+)CCR2(RFP/+) reporter mice, we show that TBI initiated a tempo

57 roglia before tMCAO in P9 Cx3cr1(GFP/+)/Ccr2(RFP/+) mice exacerbated injury and induced hemorrhages a

58 cts were independent of infiltration of Ccr2(RFP/+) monocytes into injured regions.

59 dels in combination with CX3CR1(GFP/WT);CCR2(RFP/WT) double knock-in mice.

60 ption unit activation in Cx3cr1(+/GFP)CCR2(+/RFP) knockin fluorescent protein reporter mice.

61 in myeloid cells exist, among them the CCR2-RFP and the CX3CR1GFP mouse.

62 In plant cells, CHX20-RFP co-localized with an endoplasmic reticulum marker, w

63 LdSar1 in Ldgp63 trafficking, we coexpressed RFP-Ldgp63 along with LdSar1:WT-GFP or LdSar1:T34N-GFP a

64 six transmembrane domains with the conserved RFP domain playing an integral part in ionic selectivity

65 ing dendritic cells were observed contacting RFP-expressing tumor cells with their dendrites.

66 proliferation decreased in cells containing RFP puncta, suggesting that autophagic cells are less li

67 rtment (IGC), with more glomeruli containing RFP(+)CoRL and, within these glomeruli, more RFP(+)CoRL.

68 ng approaches are discussed for conventional RFPs, far-red FPs, RFPs with a large Stokes shift, fluor

69 scence signals of all jellyfish GFP or coral RFP derivatives, respectively.

70 nant rMERS-CoV, rMERS-CoV*ORF5, and MERS-CoV-RFP replicated to high titers, whereas MERS-DeltaORF3-5

71 CXCR7 caused abnormal accumulation of CXCL12-RFP at CXCR4-positive sites in the nasal area of CXCL12-

72 4-positive sites in the nasal area of CXCL12-RFP-transgenic mice and excessive CXCL12-dependent intra

73 tural features in other maturation-deficient RFPs may result in RFPs with faster and more complete ma

74 red chromophore maturation in DsRed-derived RFPs.

75 econd group, VSV-CT1, VSV-dG-GFP, and VSV-dG-RFP, had significantly diminished toxicity toward normal

76 The vectors express either RFP or GFP markers, allowing simple in vivo tracking of

77 w fluorescent mPlum mutant to a red-emitting RFP without reverting any of the mutations causing the m

78 pressing macrophages were observed engulfing RFP-expressing cancer cells.

79 These enhanced RFPs provide new possibilities to study biological proce

80 For most imaging experiments, RFPs that mature quickly to the red chromophore and prod

81 ascending (CiA) interneurons do not express RFP.

82 ls in each randomly selected clone expressed RFP strongly.

83 ed movement and fusion than cells expressing RFP-Htt protein with 28 polyglutamine repeats.

84 Stable transgenic cell clones expressing RFP were selected with G418 sulfate and individual clone

85 one expressing GFP and the other expressing RFP, were simultaneously injected in the inguinal lymph

86 mice produce autophagic vacuoles expressing RFP and EGFP puncta.

87 uggesting that transcription is required for RFP activity.

88 iscussed for conventional RFPs, far-red FPs, RFPs with a large Stokes shift, fluorescent timers, irre

89 ations of red chromophores allows the future RFP phenotypes and their respective novel imaging applic

90 zation, whereas ST1-YFP (85 kDa) and GalNAcT-RFP (115 kDa) are broadly distributed in ER and Golgi.

91 rs (agroinfection) to express functional GBP:RFP fusion (chromobody) in the model plant Nicotiana ben

92 Most interestingly, GBP:RFP can be applied to interfere with the function of GFP

93 eated with cyclophosphamide, the HCT-116-GFP-RFP cells also survived and formed colonies in the liver

94 ost cellular system attacked the HCT-116-GFP-RFP cells but could not effectively kill the MMT-GFP-RFP

95 The data suggest rapid death of HCT-116-GFP-RFP cells in the portal vein.

96 ruction of the cytoplasm) of the HCT-116-GFP-RFP cells occurred within 6 hours.

97 Most HCT-116-GFP-RFP cells remained in sinusoids near peripheral portal v

98 Human HCT-116-GFP-RFP colon cancer and mouse mammary tumor (MMT) cells wer

99 e mammary tumor (MMT) cells were HCT-116-GFP-RFP in the portal vein of nude mice.

100 protein (RFP) in the cytoplasm (HCT-116-GFP-RFP) were injected in either the PV or spleen of nude mi

101 In contrast, dual-color MMT-GFP-RFP cells injected into the portal vein mostly survived

102 Many surviving MMT-GFP-RFP cells showed invasive figures with cytoplasmic protr

103 s but could not effectively kill the MMT-GFP-RFP cells.

104 SV-CT1/CT9), G protein deletions (VSV-dG-GFP/RFP), and combinations thereof (VSV-CT9-M51).

105 as partially restored in the presence of GFP/RFP packaging constructs.

106 enuations included gene shifting (VSV-p1-GFP/RFP), M protein mutation (VSV-M51), G protein cytoplasmi

107 upon transient transfection with GalNAcT-HA-RFP and by GFP-to-RFP FRET signals that are confined to

108 A total of 42 of 69 had RFP at rest, which reverted to non-RFP at stress in 24 (

109 er, MDA-MB-435-RFP breast cancer, and HT1080-RFP fibrosarcoma were transplanted to the transgenic GFP

110 e quest for further red-shifted and improved RFPs continues.

111 eased by 60%, 40%, and 49%, respectively, in RFP-positive Sk-Hep-1 recovered by fluorescence-activate

112 ther maturation-deficient RFPs may result in RFPs with faster and more complete maturation to the red

113 over, RAAS inhibition in FSGS mice increased RFP(+)CoRL transdifferentiation in the IGC to phenotypes

114 ersely, inhibition of mTOR complex 1 induced RFP and EGFP expression and decreased cell proliferation

115 cation; however, 17AAG prevented DEX-induced RFP-GRalpha nuclear translocation.

116 oth nuclear import and export of DEX-induced RFP-GRalpha were faster than RU-486-induced nuclear shut

117 chicine blocked DEX-induced or RU486-induced RFP-GRalpha nuclear translocation; however, 17AAG preven

118 Instead, RFP(+) cells exhibited axons descending ipsilaterally, a

119 GnRH neurons expressing actin-GFP or Lifeact-RFP, calcium release was found to stimulate leading proc

120 Comparisons with mKeima LSS RFP suggest that similar proton relays could be engineer

121 t proteins is to label whole cells, but many RFPs are cytotoxic when used with standard high-level ex

122 nt protein (RFP)-labeled peroxisomal markers RFP-peroxisome targeting signal 1 and peroxisome targeti

123 ravital multiphoton microscopy of DC(GFP)/MC(RFP) reporter mice, we herein provide in vivo evidence t

124 he dominant negative effect of the monomeric RFP-ORF23 (mRFP23) fusion protein.

125 RFP(+)CoRL and, within these glomeruli, more RFP(+)CoRL.

126 ast, mCherry fused to an internal loop (MreB-RFP(SW)) does not induce helices.

127 tate, "patchy" localization patterns of MreB-RFP(SW), even by standard light microscopy.

128 resent feasibility of an in vivo assay (NFAT-RFP) that reports transcriptional activity of NFAT via e

129 Furthermore, NFAT-RFP can be used simultaneously with NFAT-GFP fusion prot

130 TOR), which prevents autophagy, contained no RFP puncta.

131 , but persisted in 18 (EE); 27 of 69 had non-RFP at rest and peak stress (AA).

132 of 69 had RFP at rest, which reverted to non-RFP at stress in 24 (EA), but persisted in 18 (EE); 27 o

133 lutamate receptors, the intensity of the NPY-RFP-labeled puncta declined in a step-like manner indica

134 ysosome fusion measured by colocalization of RFP-LC3 and LysoSensor Green was accelerated by IGF-I.

135 37 patients with an established diagnosis of RFP (the diagnosis was proven by biopsy in 31 patients),

136 Nuclear export of RFP-GRalpha was studied using confocal microscopy follow

137 Expression of RFP accounted for viral transduction efficiency and long

138 s at E2 resulted in widespread expression of RFP throughout the spinal cord with >/=60% of Islet1/2-p

139 Imaging of RFP-tagged end binding protein 1 (EB1) and YFP-tagged al

140 till maintained a strong expression level of RFP, indicating that these transgenic cell clones were s

141 3 days after IRI, whereas the high levels of RFP puncta persisted, indicating autophagy initiation at

142 Nuclear localization of RFP-GRalpha in NTM5 cells treated with vehicle (ethanol)

143 proximal tubules, with increased numbers of RFP and EGFP puncta that peaked at 1 day after IRI.

144 Time-lapse recordings of RFP-labeled stable synaptic sites demonstrate that Dkk1

145 approximately IQD1-dependent recruitment of RFP approximately KLCR1 and RFP approximately CaM2 to mi

146 ed the B-box and first coiled-coil region of RFP together with the bHLH domain of SCL.

147 hoton Ca(2+) imaging to map the responses of RFP-positive and neighboring L2/3 neurons to whisker def

148 rossing to Rosa26:tdRFP mice, and sorting of RFP(+): glucagon(+) cells from KO mice, revealed recombi

149 retion of Ldgp63, whereas the trafficking of RFP-Ldgp63 in GFP-LdRab1:WT-expressing cells is unaltere

150 on had no effect on nuclear translocation of RFP-GRalpha.

151 cells showed robust nuclear translocation of RFP-STAT3 or STAT1-GFP, respectively.

152 The prognostic value of RFP at peak stress in ICM is unknown.

153 DNA coding for a non-fluorescent variant of RFP.

154 ch to red-shift the fluorescence emission of RFPs.

155 . maximus populations grown monoxenically on RFP labeled Escherichia coli in a soil slurry.

156 reproductive isolation, we expressed GFP or RFP in sperm heads of recently diverged sister species,

157 n (RFP) in the cytoplasm or with GFP only or RFP only were injected into the inguinal lymph node of n

158 cell-specific expression of CFP, GFP, YFP or RFP revealed the simultaneous migration of multiple podo

159 ow, or red fluorescent protein (GFP, YFP, or RFP) in F-11A cells.

160 om embryonic day 12.5 (E12.5) and E13.5 Osr2(RFP/+) and Osr2(RFP/-) mutant mouse embryos and performe

161 12.5 (E12.5) and E13.5 Osr2(RFP/+) and Osr2(RFP/-) mutant mouse embryos and performed whole transcri

162 1.5-fold at both E12.5 and E13.5 in the Osr2(RFP/-) palatal mesenchyme cells, in comparison with Osr2

163 al mesenchyme cells, in comparison with Osr2(RFP/+) littermates.

164 VSV-M51, VSV-CT9-M51, VSV-p1-GFP, and VSV-p1-RFP.

165 Furthermore, P6-RFP coimmunoprecipitated with PDLP1-GFP.

166 We examined the colocalization of P6-RFP I-LBs with PDLP1-green fluorescent protein (GFP) and

167 observed at plasmodesmata) and found that P6-RFP I-LBs were associated with each of these markers.

168 termine whether restrictive filling pattern (RFP) at peak stress has prognostic value.

169 Replication fork pause (RFP) sites transiently arresting replication fork moveme

170 We first identified a circularly permuted RFP (cpRFP) scaffold, which maintained its autocatalytic

171 toactivatable and reversibly photoswitchable RFPs.

172 d human TE85 osteosarcoma cells with the pPC-RFP expression vector using Effectene.

173 ed with shorter recurrence-free probability (RFP; P = .043), the relative proportion of stromal FoxP3

174 for the first time that Ret finger protein (RFP), a member of the TRIM family of proteins initially

175 In the other, the red fluorescence protein (RFP) gene is flanked by the native FRTs.

176 carrying the marker red fluorescent protein (RFP) and a GluA2 RNAi construct to downregulate GluA2 ex

177 017 with N-terminal red fluorescent protein (RFP) and C-terminal green fluorescent protein (GFP) reve

178 with the Discosoma red fluorescent protein (RFP) and orthotopically implanted onto the pancreas of n

179 PV(+) neurons with red fluorescent protein (RFP) and targeted them for cell-attached electrophysiolo

180 the Discomsoma sp. red fluorescent protein (RFP) and the enhanced green fluorescent protein (EGFP) r

181 in (GFP) and Myo3/5-red fluorescent protein (RFP) at nascent endocytic sites was revealed by two-colo

182 ha promoter and the red fluorescent protein (RFP) during lytic replication from the viral early PAN p

183 Indeed, red fluorescent protein (RFP) expression from mutated T-strand can be restored by

184 TH) promoter-driven red fluorescent protein (RFP) fluorescent reporter.

185 overy of functional red fluorescent protein (RFP) from DNA coding for a non-fluorescent variant of RF

186 luding an exon, and red fluorescent protein (RFP) from the mRNA lacking the exon; the other switches

187 ssion of ORF23 as a red fluorescent protein (RFP) fusion protein appeared to have a dominant negative

188 genetically fuse a red fluorescent protein (RFP) gene and two binding sites for an RNA-binding prote

189 vector, we cloned a red fluorescent protein (RFP) gene into the pPC vector at the MCS and transfected

190 T via expression of red fluorescent protein (RFP) in individual cells.

191 in the nucleus and red fluorescent protein (RFP) in the cytoplasm (HCT-116-GFP-RFP) were injected in

192 in the nucleus and red fluorescent protein (RFP) in the cytoplasm or with GFP only or RFP only were

193 in the nucleus and red fluorescent protein (RFP) in the cytoplasm.

194 leus and retroviral red fluorescent protein (RFP) in the cytoplasm.

195 was inserted into a red fluorescent protein (RFP) mCherry and a human Src tyrosine kinase to create i

196 porter mouse with a red fluorescent protein (RFP) sequence inserted into the interleukin-17F (IL-17F)

197 of exogenous Ealpha-red fluorescent protein (RFP) to the Ealpha-mCh yeast boosted the number of cytok

198 ) were labeled with red fluorescent protein (RFP) using retrograde viral infection.

199 onal RTE1 fusion to red fluorescent protein (RFP) was expressed under the control of the native RTE1

200 rafish in which the red fluorescent protein (RFP) was inserted into the pax8 gene.

201 .2 protein fused to red fluorescent protein (RFP) was localized to the plasma membrane and specifical

202 g a gene encoding a red fluorescent protein (RFP) whose expression correlates with the timing and lev

203 nt protein (GFP) or red fluorescent protein (RFP) with HA packaging regions (45 3' and 80 5' nucleoti

204 A GBP fusion to the red fluorescent protein (RFP), a molecule termed a chromobody, was previously use

205 of PV-Cre mice with red fluorescent protein (RFP), followed by targeted loose-patch recordings and tw

206 Red fluorescent protein (RFP)-expressing human cancer cell lines, including PC-3-

207 Using a red fluorescent protein (RFP)-expressing recombinant RRV (RRV-RFP), we show that

208 s effected by using red fluorescent protein (RFP)-expressing tumors growing in GFP-expressing transge

209 Stably transfected red fluorescent protein (RFP)-GRalpha NTM5 cell lines were developed.

210 ructures as well as red fluorescent protein (RFP)-labeled neurons within the mouse hippocampus are im

211 olocalizes with the red fluorescent protein (RFP)-labeled peroxisomal markers RFP-peroxisome targetin

212 olocalized with the red fluorescent protein (RFP)-tagged EV marker, CD63, after LPC treatment of cotr

213 at cells expressing red fluorescent protein (RFP)-tagged Htt protein containing 74 polyglutamine repe

214 pressing MIST1 with red fluorescent protein (RFP)-tagged pepsinogen C, a key secretory product of ZCs

215 ytes expressing NPY-red fluorescent protein (RFP).

216 AV vectors carrying red fluorescent protein (RFP).

217 c factor (BDNF) and red fluorescent protein (RFP).

218 nant RSV expressing red fluorescent protein (RFP).

219 , both small [i.e., red fluorescent protein (RFP)] and large (i.e., peroxisomes) substrates are effic

220 pH sensitivities of red fluorescent protein (RFP; pKa 4.5) and enhanced green fluorescent protein (EG

221 of spectrally distinct fluorescent proteins (RFP, YFP and CFP) in neighboring cells, creating a 'Brai

222 Red fluorescent proteins (RFPs) derived from organisms in the class Anthozoa have

223 e advanced red-shifted fluorescent proteins (RFPs) has been developed.

224 ndicators based on red fluorescent proteins (RFPs) has created new opportunities for multicolour visu

225 ion wavelengths of red fluorescent proteins (RFPs) make them attractive for whole-animal imaging beca

226 ing kinetics in 13 red fluorescent proteins (RFPs) with different chromophore environment and show th

227 ate2 are monomeric red fluorescent proteins (RFPs) with large Stokes shifts (LSSs), which allows for

228 type I elements diminish pausing at proximal RFPs.

229 vity (RSN) and relative false-positive rate (RFP) for PCR and LCR versus cell culture among 1,138 asy

230 sistent with its attenuated activities, RecA-RFP nucleates onto double-stranded DNA approximately 3-f

231 As a consequence, RecA-RFP is proficient for DNA strand exchange with dATP or a

232 he wild-type protein, the activities of RecA-RFP are further enhanced by shifting the pH to 6.2.

233 mRFP1) to produce a functional protein (RecA-RFP) that is suitable for in vivo and in vitro analysis.

234 In vitro, the purified RecA-RFP protein forms a nucleoprotein filament whose k(cat)

235 rotein is also a dATPase; dATP supports RecA-RFP nucleoprotein filament formation in the presence of

236 In vivo, the RecA-RFP partially restores UV resistance, conjugational reco

237 Thus, RecA-RFP reveals that its attenuated biological functions cor

238 y, using single molecule visualization, RecA-RFP was seen to assemble into a continuous filament on d

239 nd that the GFPNESWdr68 fusion redistributed RFP-Dyrk1a to the cell cytoplasm potentially disconnecti

240 tein levels and accumulation of LC3 reporter RFP+ GFP+ (yellow) puncta, suggesting that HIV-1 infecti

241 f GFP-LdRab1:Q67L or GFP-LdRab1:S22N retains RFP-Ldgp63 in Golgi and blocks the secretion of Ldgp63,

242 t with tomato red fluorescent protein (rMERS-RFP) or deleted the entire ORF3, 4, and 5 accessory clus

243 rotein (RFP)-expressing recombinant RRV (RRV-RFP), we show that RRV particles are colocalized with ma

244 Selective RFP tumor fluorescence enabled noninvasive real-time com

245 oci with fluorescent protein (FP) sequences (RFP and GFP respectively) by targeted integration via zi

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

247 hortcoming, we developed a long Stokes shift RFP-based Ca(2+) indicator, REX-GECO1, with optimal two-

248 ee prominent replication fork pausing sites (RFPs) located in or immediately adjacent to nucleosome-f

249 endosomes, because they colocalize with Snf7-RFP and because they correspond to a perivacuolar compar

250 Advantages and limitations of specific RFPs for each technique are presented.

251 Doppler echocardiography at rest and stress; RFP was defined as transmitral E:A ratio > or =1.0, isov

252 termined binding of GFP-tagged CaMKII to tag-RFP-labeled actin cytoskeleton within live cells using t

253 t protein (GFP) revealed that the N-terminal RFP domain migrated into the nucleus, while the C-termin

254 -clamp recordings of DA amacrine cells in TH-RFP mice and M1 ipRGCs in OPN4-EGFP mice.

255 brain dopaminergic neurons obtained from TH::RFP mice, immortalized DA neurons, and a heterologous sy

256 cal recordings of fluorescent neurons in TH::RFP (tyrosine hydroxylase gene promoter::red fluorescent

257 ses, and sequence analysis demonstrated that RFP was expressed from the appropriate consensus sequenc

258 ination of the axon morphology revealed that RFP(+) neurons include commissural bifurcating longitudi

259 When GFP spleen cells and the RFP cancer cells were coinjected in the PV, liver metast

260 In contrast, the RFP(+) cells of pax2a/pax8 double mutants displayed alte

261 eek-old Emu-ret mice, which also express the RFP/RET transgene, differentiate in IL-7 similarly to th

262 In pax8 homozygous fish, the RFP(+) cells underwent differentiation similar to that o

263 The luciferase insertion was made in the RFP-STAT3/STAT1-GFP cell line to have all three reporter

264 ing protein, whose translated product is the RFP protein alone.

265 ffects in the conformational dynamics of the RFP chromophore.

266 ortional to the associated expression of the RFP protein.

267 mphocytes were seen surrounding cells of the RFP tumor, which eventually regressed.

268 e results suggest that the expression of the RFP/RET transgene initially prevents the normal eliminat

269 e readily distinguished interacting with the RFP-expressing tumor cells.

270 e relationship between the properties of the RFPs of different phenotypes and their applications to v

271 ansfection with GalNAcT-HA-RFP and by GFP-to-RFP FRET signals that are confined to the Golgi.

272 Tumor RFP fluorescence facilitated real-time, sequential imagi

273 RNA oligonucleotides with partial wild-type RFP sequence, implying the involvement of plant DNA repa

274 lls expressing red fluorescent protein (U251-RFP) in zebrafish embryos.

275 After injection into the embryos, the U251-RFP cells proliferated and the resultant tumors, and eve

276 RFP-FimXDeltaREC, unlike RFP-FimX, is no longer localized to the bacterial pole,

277 Although several useful RFPs have been developed using directed evolution, the q

278 ors differentially tagged with GFP variants (RFP and YFP) provided evidence for the close proximity o

279 ith an endoplasmic reticulum marker, whereas RFP-tagged CHX17-CHX19 co-localized with prevacuolar com

280 To address this, we generated a fly in which RFP-Moesin and GFP-Moesin are expressed in mutually excl

281 ivo we find that EHBP-1-GFP colocalizes with RFP-RAB-10 on endosomal structures of the intestine and

282 by a previously undescribed interaction with RFP, which functions to recruit HDAC and/or Polycomb pro

283 vector is used for cytoplasmic labeling with RFP.

284 icol acetyltransferase, and thioredoxin with RFP, respectively, further substantiates the general app

285 NTM5 cells transfected with RFP-GRalpha showed a clear cytosolic localization of rec

286 7R was associated with worse outcome (5-year RFP, 76% for high v 86% for low expression; P = .001).

287 s a stronger predictor of recurrence (5-year RFP, 85% for high v 77% for low ratio; P = .004).

288 ) was associated with better outcome (5-year RFP, 90% for high v 80% for low expression; P = .026), w

289 ronments can be rationally modified to yield RFPs with novel photochemical properties.