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1 f the PMCA by CaM fluorescently labeled with tetramethylrhodamine.
2 a dextran conjugated to Oregon Green 488 and tetramethylrhodamine.
3 side GM1 was tagged with the fluorescent dye tetramethylrhodamine.
4 zymosan conjugate containing fluorescein and tetramethylrhodamine.
5 conjugate containing Oregon Green(R) 488 and tetramethylrhodamine.
6 do carbocyanine perchlorate, or chloromethyl tetramethylrhodamine.
7 oltage indicators based on isomerically pure tetramethylrhodamines.
8                       Linear dichroism of 5'-tetramethylrhodamine (5'ATR)-labeled cardiac troponin C
9 res tetramethylrhodamine (TMR) and 5-carboxy-tetramethylrhodamine (5-TAMRA) with nanomolar affinity.
10                   The binding and bending of tetramethylrhodamine-5'-(GGGCTATAAAAGGG) duplex-3'-fluor
11 rescein-5-isothiocyanate (FITC) as donor and tetramethylrhodamine-5- (and 6-) isothiocyanate (TRITC)
12 ed cardiac TnC mutant labeled at Cys-84 with tetramethylrhodamine-5-iodoacetamide dihydroiodide was p
13 ith 8-anilino-1-naphthalenesulfonic acid and tetramethylrhodamine-5-iodoacetamide.
14 rome c through its single free cysteine with tetramethylrhodamine-5-maleimide (TMR), a fluorophore wi
15         With the Tb chelate as the donor and tetramethylrhodamine-5-maleimide as the acceptor, both b
16 e been derivatized with a fluorescent probe, tetramethylrhodamine-5-maleimide, for biophysical studie
17    A comparison of this structure to that of tetramethylrhodamine-5-maleimide-actin with bound ADP, d
18               The x-ray crystal structure of tetramethylrhodamine-5-maleimide-actin with bound AMPPNP
19 fluorescein label (6-FAM) and a 3',6-carboxy-tetramethylrhodamine (6-TAMRA) label: 6-FAM-dArUdAdA-6-T
20 yl-lysine residue, with a fluorescent group (tetramethylrhodamine-6-carboxylic acid, 6-TAMRA) near th
21 ed in Xenopus laevis oocytes and tagged with tetramethylrhodamine-6-maleimide (TMR6M).
22 dent fluorescence changes upon labeling with tetramethylrhodamine-6-maleimide (TMRM), which were due
23  environmentally sensitive fluorescent probe tetramethylrhodamine-6-maleimide (TMRM).
24  laevis oocytes, cysteines were labeled with tetramethylrhodamine-6-maleimide, and voltage-dependent
25 methanethiosulfonate but was inaccessible to tetramethylrhodamine-6-maleimide.
26 ed with fluorescein (a pH-sensitive dye) and tetramethylrhodamine (a pH-insensitive dye), which serve
27 led with either fluorescein (donor probe) or tetramethylrhodamine (acceptor probe) and then used to m
28 ) conjugation of F239C in the large lobe and tetramethylrhodamine (acceptor) conjugation of C343 in t
29  separate pools with fluorescein (donor) and tetramethylrhodamine (acceptor).
30 ubunit tetramethylrhodamine dimers form when tetramethylrhodamine acetamide is attached to two differ
31 f the yeast Bni1p FH2 domain in complex with tetramethylrhodamine-actin.
32 ing of DNA with some fluorescent dyes, e.g., tetramethylrhodamine, alters DNA density on AuNP.
33 nt experiment, dextran (10K) conjugated with tetramethylrhodamine and biotin was injected into the no
34 e N-terminus of mutant LC1, was labeled with tetramethylrhodamine and exchanged into skeletal subfrag
35 f amplified DNA labeled with the fluorophore tetramethylrhodamine and the AP-1 consensus nucleotide s
36 ugated prestin to a photostable fluorophore (tetramethylrhodamine) and performed single-molecule fluo
37 a complementary oligonucleotide labeled with tetramethylrhodamine, and monitored over time for quench
38  was generated, labeled with the fluorophore tetramethylrhodamine, and subjected to various anisotrop
39 inergic M(3) receptor ligands to fluorescent tetramethylrhodamine- and cyanine-5-type dyes, two novel
40 able conjugates with biotin, digoxigenin and tetramethylrhodamine are described.
41 luorescein as a pH-dependent fluorophore and tetramethylrhodamine as a pH-independent fluorophore.
42        In this method, Abeta is labeled with tetramethylrhodamine at a lysine residue on the N-termin
43 pen binding pocket harboring the xanthene of tetramethylrhodamine at the tip, while the dinitroanilin
44 ulfonic acid at Cys-190 of Tm and phalloidin-tetramethylrhodamine B isothiocyanate bound to F-actin.
45 e peptides that has been labeled with BODIPY-tetramethylrhodamine (BODIPY(TMR)).
46 maleimide and a membrane-impermeant 2-((5(6)-tetramethylrhodamine)carboxylamino) ethyl methanethiosul
47 is of TM1 with biotin maleimide and 2-((5(6)-tetramethylrhodamine)carboxylamino) ethyl methanethiosul
48 tin maleimide (BM)) and impermeant (2-((5(6)-tetramethylrhodamine)carboxylamino)ethyl methanethiosulf
49 s, anterogradely labeled with biotin dextran tetramethylrhodamine, caudal to the lesion.
50 analog of CGP 12177 [bordifluoropyrromethane-tetramethylrhodamine-(+/-)CGP 12177 (BODIPY-TMR-CGP)] at
51 agglutinin-horseradish peroxidase or dextran-tetramethylrhodamine conjugated to biotin.
52 ached to a single cysteine on the serpin and tetramethylrhodamine conjugated to the proteinase.
53                            Binding of L7/L12:tetramethylrhodamine cysteine 33 or cysteine 12 dimers e
54                                            A tetramethylrhodamine derivative of I(A) was prepared and
55 ated cardiac myocytes via photoactivation of tetramethylrhodamine derivatives, which also served to r
56 cells were allowed to endocytose fluorescein tetramethylrhodamine dextran (FRD), a ratiometric probe
57 erent ages received injections of the tracer tetramethylrhodamine dextran (TMR-D) into the nodose gan
58 ganglion cell layer using Nissl staining and tetramethylrhodamine dextran amine backfilling.
59 lus vulgaris leucoagglutinin, Fluoro-Gold or tetramethylrhodamine dextran amine into either the vesti
60  were identified by retrograde labeling with tetramethylrhodamine dextran amine.
61                                              Tetramethylrhodamine dextran and cholera toxin B uptake
62 ion of a 1.5-microL solution of 0.25% 70-kDa tetramethylrhodamine-dextran (TMR-D).
63            Transscleral permeation by 10-kDa tetramethylrhodamine-dextran also was determined, for co
64 IT-type neurons were retrogradely labeled by tetramethylrhodamine-dextran amine (RDA)3k injection int
65            Transscleral permeation by 10-kDa tetramethylrhodamine-dextran was 1.04 +/- 0.39 x 10(-6)
66                             The formation of tetramethylrhodamine dimers caused the appearance of a n
67                                          The tetramethylrhodamine dimers disappear rapidly (within 5
68                                          The tetramethylrhodamine dimers do form at sites in the C-te
69                                 Ground-state tetramethylrhodamine dimers form between the two subunit
70                                 Intersubunit tetramethylrhodamine dimers form when tetramethylrhodami
71 uencher conformation for both free and bound tetramethylrhodamine-dinitroaniline being predominant.
72 tetramethylrhodamine to unquench the RhoBAST-tetramethylrhodamine-dinitroaniline complex.
73 crystal structure of RhoBAST in complex with tetramethylrhodamine-dinitroaniline to elucidate the mol
74 activates the fluorophore-quencher conjugate tetramethylrhodamine-dinitroaniline with high affinity,
75 conformation significantly decreases in free tetramethylrhodamine-dinitroaniline.
76              A fast cleaving non-nucleosidic tetramethylrhodamine dye-labeled support has been develo
77                   In hepatocytes loaded with tetramethylrhodamine ethyl ester (10 nM) to quantify mit
78                                              Tetramethylrhodamine ethyl ester (TMRE) and 2',7'-dichlo
79 ificantly decreased cellular accumulation of tetramethylrhodamine ethyl ester (TMRE) and daunorubicin
80  employing the fluorescent lipophilic cation tetramethylrhodamine ethyl ester (TMRE) as a noninvasive
81 etramethylrhodamine methyl ester (TMRM), and tetramethylrhodamine ethyl ester (TMRE) as fluorescent p
82 ucose (2-NBDG) reports on glucose uptake and Tetramethylrhodamine ethyl ester (TMRE) reports on mitoc
83  was assessed by flow cytometric analysis of tetramethylrhodamine ethyl ester (TMRE)-loaded cells.
84 nd intact cells using the fluorescent probe, tetramethylrhodamine ethyl ester (TMRE).
85  with a fluorescent Delta(Psi)(m)-indicator, tetramethylrhodamine ethyl ester (TMRE).
86 (m)), as assessed by the potentiometric dye, tetramethylrhodamine ethyl ester (TMRE).
87 ific probe for mitochondrial calcium; and of tetramethylrhodamine ethyl ester fluorescence to monitor
88 ciated with significantly attenuated loss of tetramethylrhodamine ethyl ester fluorescence under basa
89            Consistent with this observation, tetramethylrhodamine ethyl ester perchlorate staining re
90 were monitored using ratiometric pericam and tetramethylrhodamine ethyl ester probe, respectively, to
91  potential (with the potential-sensitive dye tetramethylrhodamine ethyl ester) and in mitochondrial [
92 ous stimuli were assessed by flow cytometry (tetramethylrhodamine ethyl ester).
93 deprivation (OGD) and monitored psi(m) using tetramethylrhodamine ethyl ester.
94 ntial, as monitored by the fluorescent probe tetramethylrhodamine ethyl ester.
95  fluorescence arising from flavoproteins and tetramethylrhodamine ethyl ester.
96 ed with the membrane potential-sensitive dye tetramethylrhodamine-ethyl ester (TMRE) in murine viment
97 drial membrane potential-independent dye and tetramethylrhodamine-ethyl-ester-perchlorate (TMRE) and
98 nd double-stained with MitoTracker Green and tetramethylrhodamine-ethyl-ester-perchlorate were examin
99 in mitochondrial potential as assessed using tetramethylrhodamine ethylester (TMRE).
100 mitochondrial depolarization, assessed using tetramethylrhodamine ethylester, and reactive oxygen spe
101 ssessed by using the potential-sensitive dye tetramethylrhodamine ethylester.
102 ne, phOx) and fluorescent probes (Bodipy Fl, tetramethylrhodamine, fluorescein) were bound with high
103 samine (UDP-GalNAz) that is then linked to a tetramethylrhodamine fluorescent tag and CTD110.6 and RL
104 ear optical calibration curve for 5-carboxyl-tetramethylrhodamine from the concentration detection li
105 ptor coactivator 4 prevented accumulation of tetramethylrhodamine-Halo fragment and degradation of en
106 labeling experiments with the cell-permeable tetramethylrhodamine HaloTag ligand.
107 ed with a single fluorophore (fluorescein or tetramethylrhodamine) have been used previously as fluor
108 roaniline quencher stacks over the phenyl of tetramethylrhodamine instead of being fully released.
109                      Correlation analysis of Tetramethylrhodamine intensity fluctuations reveals hing
110                        The fluorescent probe tetramethylrhodamine iodoacetamide was attached to cyste
111 our DNA nucleotides labeled identically with tetramethylrhodamine is described and demonstrated.
112 orms, fluorescein isothiocyanate (F-ITC) and tetramethylrhodamine isothiocyanate (TR-ITC).
113 rophores (fluorescein isothiocyanate (FITC), tetramethylrhodamine isothiocyanate (TRITC), and carboxy
114 in isothiocyanate dextran (FITC-dextran) and tetramethylrhodamine isothiocyanate concanavalin A (TRIT
115 olecule fluorescence spectroscopy and bear a tetramethylrhodamine isothiocyanate fluorescent tag for
116                              The system uses tetramethylrhodamine isothiocyanate labeled asialofetuin
117  Golgi apparatus, BODIPY-ceramide and TRITC (tetramethylrhodamine isothiocyanate)-labeled cholera tox
118 luorescein isothiocyanate (FITC)-dextran and tetramethylrhodamine isothiocyanate-AG encapsulated in m
119 n investigated using two fluorescent probes, tetramethylrhodamine isothiocyanate-labeled phalloidin b
120 r by altering the C terminus of actin with a tetramethylrhodamine label.
121  the fluorescently labeled glycosphingolipid tetramethylrhodamine labeled GM1 (GM1-TMR) produced by s
122 ared with static counterparts, retaining the tetramethylrhodamine-labeled alpha-bungarotoxin on the m
123 ectrokinetic chromatography separation of 19 tetramethylrhodamine-labeled amino acids was accomplishe
124 as measured by dichroism of 5' iodoacetamido-tetramethylrhodamine-labeled cardiac troponin C.
125 , the measured steady-state polarizations of tetramethylrhodamine-labeled dATP, dCTP, dGTP and dUTP w
126                             We report that a tetramethylrhodamine-labeled dimer of the cell-penetrati
127                                            A tetramethylrhodamine-labeled glycosphingolipid (GM1-TMR)
128 ebella neurons was probed by incubation with tetramethylrhodamine-labeled GM1 (GM1-TMR).
129 elective LPS sensor, developed by assembling tetramethylrhodamine-labeled LPS-binding peptides on gra
130      The binding and unbinding of individual tetramethylrhodamine-labeled neutravidin molecules is me
131 e next correct dNTP; with Klenow polymerase, tetramethylrhodamine-labeled probes increased their fluo
132                             Fluorescein- and tetramethylrhodamine-labeled probes of identical sequenc
133                                              Tetramethylrhodamine-labeled rPfP2 protein exhibited DTT
134                       In these measurements, tetramethylrhodamine-labeled, anti-trinitrophenyl IgE an
135 m hydrolyze LacNAc from Galbeta1-4GlcNAcbeta-tetramethylrhodamine (LacNAc-TMR (Galbeta1-4GlcNAcbeta(C
136 hen were incubated with 10 or 70 kDa dextran-tetramethylrhodamine-lysine for 16 to 32 minutes at 37 d
137 re, we labeled the OCP of Synechocystis with tetramethylrhodamine-maleimide (TMR) and obtained a phot
138 approach to measure relative fluorescence of tetramethylrhodamine methyl ester (TMRM) and absolute va
139 approach to measure relative fluorescence of tetramethylrhodamine methyl ester (TMRM) and absolute va
140                                              Tetramethylrhodamine methyl ester (TMRM) is a fluorescen
141 otential (DeltaPsiP) and the DeltaPsiM probe tetramethylrhodamine methyl ester (TMRM) using fluoresce
142 nvestigated the use of rhodamine 123 (R123), tetramethylrhodamine methyl ester (TMRM), and tetramethy
143 /ml) were incubated in multiwell plates with tetramethylrhodamine methyl ester (TMRM, 1 microM), a po
144 focal microscopy using the fluorescent dyes, tetramethylrhodamine methyl ester and 5,6-carboxy-2',7'-
145 itochondrial membrane potential monitored by tetramethylrhodamine methyl ester decreased abruptly in
146     The fibres were then loaded with the dye tetramethylrhodamine methyl ester perchlorate (TMRM) to
147 , hepatocytes were coloaded with calcein and tetramethylrhodamine methyl ester to visualize onset of
148          The method uses the fluorescent dye tetramethylrhodamine methyl ester, which equilibrates in
149 ement of mitochondrial membrane potential by tetramethylrhodamine methyl ester.
150  potential were revealed using Fluo-4 AM and tetramethylrhodamine, methyl ester, perchlorate (TMRM) f
151 on were visualized by confocal microscopy of tetramethylrhodamine methylester (TMRM) and quenching of
152 copy of the potential-indicating fluorophore tetramethylrhodamine methylester (TMRM).
153 axons of chick sensory neurons using the dye tetramethylrhodamine methylester (TMRM).
154 chondrial membrane potential-indicating dye, tetramethylrhodamine methylester.
155 e microcapsules loaded with different loads (tetramethylrhodamine-modified dextran, TMR-D; microperox
156 al deoxynucleotidyltransferase-mediated dUTP-tetramethylrhodamine nick end labeling assay, demonstrat
157 sonance energy transfer donor and anti-actin tetramethylrhodamine phalloidin as an acceptor.
158                            For this purpose, Tetramethylrhodamine probes were introduced at pairs of
159  O2 both sensors are chemically converted to tetramethylrhodamine, producing significant (>/=66 nm) b
160  to dextran, together with a red fluorescing tetramethylrhodamine reference chromophore.
161 mples of rhodamines and rosamines, including tetramethylrhodamine, rhodamine B, and Janelia Fluor 549
162 -vis spectrum of the beta-clamp labeled with tetramethylrhodamine shows the characteristic absorption
163 s were 1 zmol for BODIPY-FL and 500 ymol for tetramethylrhodamine standard solutions.
164 00,000 theoretical plates in 6-14 s for both tetramethylrhodamine succidimidyl ester and fluorescein-
165 ction to simultaneously incorporate an azido-tetramethylrhodamine (TAMRA) fluorophore and an aminooxy
166 ed the zwitterionic, membrane-impermeant dye tetramethylrhodamine (TAMRA) into cells even when the co
167 d 70 kDa dextran, 10 kDa dextran, and 467 Da tetramethylrhodamine (TAMRA) was examined under diffusiv
168 DNA labeled with either fluorescein (FAM) or tetramethylrhodamine (TAMRA) with a metal surface, using
169                 In this work fluorescein and tetramethylrhodamine (TAMRA), a Forster resonance energy
170 mparison of Texas Red (TR), fluorescein, and tetramethylrhodamine (TAMRA)-labeled aptamers reveals su
171 intracellular CXCR2 antagonist 00767013 (1), tetramethylrhodamine (TAMRA)-labeled CXCR2 ligands were
172                                            A tetramethylrhodamine-Tat conjugate is effectively transl
173 ng either the fluorescein-thiourea (7a-c) or tetramethylrhodamine-thiourea (9a,b) moieties were also
174 nrichment (SELEX) and binds the fluorophores tetramethylrhodamine (TMR) and 5-carboxy-tetramethylrhod
175                      Noncovalently "stacked" tetramethylrhodamine (TMR) dimers have been used to both
176                             On this basis, a tetramethylrhodamine (TMR) labeled tracer was synthesize
177 tides labeled at their N-termini with either tetramethylrhodamine (TMR) or 7-nitrobenz-2-oxa-1,3-diaz
178                          The fluorescent dye tetramethylrhodamine (TMR) was conjugated to a synthetic
179 it[7]uril (Q7) linked to the fluorescent dye tetramethylrhodamine (TMR), and the characterization of
180 poration of the high molecular weight marker tetramethylrhodamine (TMR)-dextran and its blockage by t
181                                              Tetramethylrhodamine (TMR)-doped silica nanoparticles, e
182 ally sensitive fluorescent rhodamines [e.g., tetramethylrhodamine (TMR)-thiols].
183 ed fluorescent Cl(-)-insensitive chromophore tetramethylrhodamine (TMR).
184 beled at its N terminus with the fluorophore tetramethylrhodamine (TMR).
185  the C0-C2 fragment of cMyBP-C (cC0-C2) with tetramethylrhodamine (TMR).
186 s selected to bind a larger fluorescent dye, tetramethylrhodamine (TMR).
187 ed within a cell of interest and reacts with tetramethylrhodamine (TMR; its ligand attached to a fluo
188 neous fluorescent labeling with a green dye (tetramethylrhodamine, TMR) and attachment to microbeads.
189  effectively depolarized by diazoxide (-15%, tetramethylrhodamine [TMRM]), less so by levcromakalim,
190 us using the in vitro application of dextran-tetramethylrhodamine to the pituitary.
191  6-methoxyquinoline and chloride-insensitive tetramethylrhodamine to the zymosan particles.
192 ce of releasing dinitroaniline from xanthene tetramethylrhodamine to unquench the RhoBAST-tetramethyl
193 n transport protein transferrin labeled with tetramethylrhodamine undergoes rapid receptor-mediated e
194 of actin made monomeric by modification with tetramethylrhodamine, which show formation of an alpha-h
195 e [(5-(and-6)-((4-chloromethyl)benzoyl)amino)tetramethylrhodamine], which allowed estimation of the g
196 placed the N,N-dimethylamino substituents in tetramethylrhodamine with four-membered azetidine rings.
197 eling on Plk1 and Plk3 targeted by AX7503, a tetramethylrhodamine-wortmannin conjugate.
198 s, biotin-wortmannin, BODIPY-wortmannin, and tetramethylrhodamine-wortmannin.

 
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