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1 an acetyl H3K9-specific scFv, tethered to a cyan fluorescent protein.
2 escent protein with the chloride-insensitive cyan fluorescent protein.
3 tro assays and cells overexpressing stathmin-cyan fluorescent protein.
4 ergy transfer (FRET) acceptor for the newest cyan fluorescent proteins.
5 tein kinase A (PKA) consisting of fusions of cyan fluorescent protein, a phosphoamino acid binding do
6 nced yellow fluorescent protein and enhanced cyan fluorescent protein, allowing detection of zinc-ind
7 ore, the septin Cdc12p, fused with yellow or cyan fluorescent protein, also colocalized with Myo1p an
9 otransfected with a mitochondrially targeted cyan fluorescent protein and an enhanced yellow fluoresc
10 onstrated by podocyte specific expression of cyan fluorescent protein and by electron microscopy.
11 red the interaction between DDR1 tagged with cyan fluorescent protein and DDR1 tagged with yellow flu
13 ged the TAP1 and TAP2 subunits with enhanced cyan fluorescent protein and enhanced yellow fluorescent
15 our method, we targeted QDs to cell surface cyan fluorescent protein and epidermal growth factor rec
16 human embryonic kidney 293T cells using H1R-cyan fluorescent protein and H2R-yellow fluorescent prot
18 omain of InsP3 receptors (types 1-3) between cyan fluorescent protein and yellow fluorescent protein
19 ding the human CrkII1-236 sandwiched between cyan fluorescent protein and yellow fluorescent protein,
20 ing VP22 and VP13/14 as fusion proteins with cyan fluorescent protein and yellow fluorescent protein,
21 tes inserted into a linker region separating cyan fluorescent protein and yellow fluorescent protein.
22 ubunits were genetically fused with enhanced cyan fluorescent protein and/or enhanced yellow fluoresc
23 f Escherichia coli K12 was flanked with CFP (cyan fluorescent protein) and YFP (yellow fluorescent pr
24 uorescence resonance energy transfer between cyan fluorescent protein- and yellow fluorescent protein
25 nce resonance energy transfer (FRET) between cyan fluorescent protein- and yellow fluorescent protein
26 icistronic mRNAs encoding enhanced green and cyan fluorescent proteins as the first and second cistro
27 he unresolved amino-terminus and cerulean, a cyan fluorescent protein, as a tag at the carboxyl-termi
28 s luciferase, yellow fluorescent protein, or cyan fluorescent protein at the carboxyl terminus of VPA
29 on of calmodulin within Citrine or fusion of cyan fluorescent protein, calmodulin, a calmodulin-bindi
30 e resonance energy transfer between enhanced cyan fluorescent protein-CaM and Na(V)1.5(4X) channels t
31 mouse liver sections after co-expression of cyan fluorescent protein-CCRP and yellow fluorescent pro
32 ts of yellow fluorescent protein (Venus) and cyan fluorescent protein (Cerulean) flank either the ent
33 reticulum Ca2+-ATPase (SERCA) were fused to cyan fluorescent protein (CFP) and coexpressed with PLB
34 maging to detect the proximity between CXCR1-cyan fluorescent protein (CFP) and fluorescence probes t
35 n a pixel-by-pixel basis using EGFR fused to cyan fluorescent protein (CFP) and Grb2 fused to yellow
36 FP-APP-YFP [containing the fluorescent tags, cyan fluorescent protein (CFP) and yellow fluorescent pr
39 r resonance energy transfer (FRET) pair, the cyan fluorescent protein (CFP) and yellow fluorescent pr
40 sfer (FRET) pairs with distinct spectra: (a) cyan fluorescent protein (CFP) and yellow FP (YFP), and
41 nsfer (FRET) of beta1a subunits labeled with cyan fluorescent protein (CFP) and/or yellow fluorescent
44 odel cell system and the standard FRET pair, cyan fluorescent protein (CFP) as the donor and yellow f
45 length Kir6.2 subunits were linked to YFP or cyan fluorescent protein (CFP) at N or C termini, and al
46 nalysis of the subcellular localization of a cyan fluorescent protein (CFP) fusion and a protein-prot
47 ellow fluorescent protein (YFP) and enhanced cyan fluorescent protein (CFP) genes in which recombinat
50 epithelial (LLCPK) cells expressing stathmin-cyan fluorescent protein (CFP) or injected with stathmin
51 of Grb2, Shc, H-Ras, and K-Ras with enhanced cyan fluorescent protein (CFP) or yellow fluorescent pro
52 -length and truncated forms of VacA fused to cyan fluorescent protein (CFP) or yellow fluorescent pro
54 ignalling (RGS4) proteins were each fused to cyan fluorescent protein (CFP) or yellow fluorescent pro
55 by two nonfluorescent fragments (N and C) of cyan fluorescent protein (CFP) or yellow fluorescent pro
56 with various vector combinations to express cyan fluorescent protein (CFP) or YFP fused to either bi
58 otein of 25 kDa (SNAP-25), were used to link cyan fluorescent protein (CFP) to yellow fluorescent pro
59 nal ribosome entry sequence (IRES)-dependent cyan fluorescent protein (CFP) translation were monitore
61 strain was used, containing a construct with cyan fluorescent protein (CFP) under Thy-1 promoter cont
62 otein (YFP) was fused to the N terminus, and cyan fluorescent protein (CFP) was fused to the C termin
64 xtended with a transmembrane (TM) domain and cyan fluorescent protein (CFP) were immobilized in the p
66 variants of green fluorescent protein (GFP), cyan fluorescent protein (CFP), and yellow fluorescent p
67 ROSA(tdTom), tryptophan hydroxylase 1 (Tph1)-cyan fluorescent protein (CFP), c-Kit(wsh/wsh), and Neur
68 ensor is composed of an end-to-end fusion of cyan fluorescent protein (CFP), chicken metallothionein
69 lly confirmed by measurements on mixtures of cyan fluorescent protein (CFP), citrine ((Cit) a yellow
70 icroscopic measurements of fluorescence from cyan fluorescent protein (CFP), citrine, and linked CFP-
72 ter resonance energy transfer (FRET) between cyan fluorescent protein (CFP)- and yellow fluorescent p
73 nance energy transmission (FRET) analysis of cyan fluorescent protein (CFP)-arm-CTD-yellow fluorescen
74 raction between MacMARCKS and dynamitin with cyan fluorescent protein (CFP)-conjugated dynamitin as t
78 Finally, the level and rate of recovery of cyan fluorescent protein (CFP)-M1-5 were lower than thos
82 performed following transient expression of cyan fluorescent protein (CFP)-tagged proteins and incub
86 thesis, cDNA constructs were created to fuse cyan-fluorescent protein (CFP) to the N terminus of SERC
87 us 2 (rAAV2) vectors encoding CIP fused with cyan-fluorescent-protein (CFP), with or without nuclear
88 uced intracellular redistribution of an EGFR-cyan fluorescent protein chimera was markedly reduced by
91 (FRET) between fusion proteins labeled with cyan fluorescent protein (donor) and yellow fluorescent
92 c for XOPS-mCFP, a membrane-targeted form of cyan fluorescent protein driven by the Xenopus rhodopsin
93 in cells expressing the fusion protein CFP (cyan fluorescent protein)-dynamitin or CFP-MB (the MacMA
94 c mice expressing a synaptotagmin 1-enhanced cyan fluorescent protein (ECFP) fusion protein under con
95 llow fluorescent protein (EYFP) and enhanced cyan fluorescent protein (ECFP) variants of green fluore
96 id carrying the gene coding for the enhanced cyan fluorescent protein (ECFP) was also introduced into
97 protein (EYFP), Ht31 was linked to enhanced cyan fluorescent protein (ECFP), and these constructs we
98 rescent protein (GFP), a variant of enhanced cyan fluorescent protein (ECFP), has been determined to
99 yellow fluorescent protein (EYFP) > enhanced cyan fluorescent protein (ECFP), while a GST construct t
100 anced green fluorescent protein- or enhanced cyan fluorescent protein (ECFP)-tagged phospholipase Cde
106 that contained enhanced yellow and enhanced cyan fluorescent protein (EYFP and ECFP, respectively) l
107 and double label (yellow fluorescent protein/cyan fluorescent protein) fluorescence labeling experime
108 e dynamic range and a 10% increase in donor (cyan fluorescent protein) fluorescence upon bleach of ye
109 assays in plants that constitutively express cyan fluorescent protein fused to histone 2B provides en
110 uorescence resonance energy transfer between cyan fluorescent protein-fused and yellow fluorescent pr
111 an be rescued by overexpression of the PEX12-cyan fluorescent protein fusion protein, which targets t
112 oxisomes, as demonstrated for endogenous and cyan fluorescent protein fusion proteins by fluorescence
114 tween Gialpha-yellow fluorescent protein and cyan fluorescent protein-Gbeta chimeras in HeLa cells.
115 al microscopy of coexpressed YFP-hGRbeta and cyan fluorescent protein-hGRalpha in COS-1 cells indicat
116 ed from phagocytic cups earlier than did p85-cyan fluorescent protein, indicating that SHIP-1 inhibit
117 almodulin, and the FRET donor ECFP (enhanced cyan fluorescent protein) into eNOS at a site adjacent t
118 The advantage over previous constructs using cyan fluorescent protein is that our construct can be us
119 ne the stability of complexes formed between cyan fluorescent protein-labeled alpha(2A)-adrenorecepto
120 fluorescent protein (YFP) move along tubulin-cyan fluorescent protein-labeled microtubules in respons
122 nally, chimeric proteins containing enhanced cyan fluorescent protein linked to wild-type CREB or CRE
126 low fluorescent protein (EYFP)- and enhanced cyan fluorescent protein-NHPX fusions, we show here that
128 s were addressed by tagging tapasin with the cyan fluorescent protein or yellow fluorescent protein (
129 ent colocalization of Akt2 fused with either cyan fluorescent protein or yellow fluorescent protein t
130 E12, E47, E12(NLS), or MyoD(NLS) and either cyan fluorescent protein or yellow fluorescent protein,
131 a fluorescently tagged P-glycoprotein (MDR1-cyan fluorescent protein) permitted the drug-resistant p
133 gion was used to introduce green, yellow and cyan fluorescent protein reporters into B. burgdorferi.
134 ciation with SERCA, measured by FRET between cyan fluorescent protein-SERCA and yellow fluorescent pr
136 sonance energy transfer was detected between cyan fluorescent protein-tagged DAT and yellow fluoresce
138 Co-expression of hemagglutinin-tagged and cyan fluorescent protein-tagged UGT1A proteins, followed
141 een genetically attached enhanced yellow and cyan fluorescent protein to the N or C terminus of the c
142 nsgenic mice in which red, green, yellow, or cyan fluorescent proteins (together termed XFPs) were se
143 gitudinal retinal imaging of mice expressing cyan fluorescent protein under control of the Thy-1 prom
145 cts were used to express SNAP-25 tagged with cyan fluorescent protein, VAMP-2 tagged with yellow fluo
146 t the Trp66 position in the chromophore of a cyan fluorescent protein variant (CFP6) to investigate t
148 used to either yellow fluorescent protein or cyan fluorescent protein we can observe tau fusion prote
149 cell lines stably coexpressing PML-enhanced cyan fluorescent protein with other individual marker pr
150 protein-Dictyostelium myosin II motor domain-cyan fluorescent protein (YFP-myosin-CFP) and compared t
151 his upregulation, we incorporated yellow and cyan fluorescent proteins (YFPs and CFPs) into the alpha