ライフサイエンスコーパス: tetramethylrhodamine

1 a dextran conjugated to Oregon Green 488 and tetramethylrhodamine.

2 side GM1 was tagged with the fluorescent dye tetramethylrhodamine.

3 zymosan conjugate containing fluorescein and tetramethylrhodamine.

4 conjugate containing Oregon Green(R) 488 and tetramethylrhodamine.

5 do carbocyanine perchlorate, or chloromethyl tetramethylrhodamine.

6 f the PMCA by CaM fluorescently labeled with tetramethylrhodamine.

7 oltage indicators based on isomerically pure tetramethylrhodamines.

8 Linear dichroism of 5'-tetramethylrhodamine (5'ATR)-labeled cardiac troponin C

9 The binding and bending of tetramethylrhodamine-5'-(GGGCTATAAAAGGG) duplex-3'-fluor

10 rescein-5-isothiocyanate (FITC) as donor and tetramethylrhodamine-5- (and 6-) isothiocyanate (TRITC)

11 ed cardiac TnC mutant labeled at Cys-84 with tetramethylrhodamine-5-iodoacetamide dihydroiodide was p

12 ith 8-anilino-1-naphthalenesulfonic acid and tetramethylrhodamine-5-iodoacetamide.

13 rome c through its single free cysteine with tetramethylrhodamine-5-maleimide (TMR), a fluorophore wi

14 With the Tb chelate as the donor and tetramethylrhodamine-5-maleimide as the acceptor, both b

15 e been derivatized with a fluorescent probe, tetramethylrhodamine-5-maleimide, for biophysical studie

16 A comparison of this structure to that of tetramethylrhodamine-5-maleimide-actin with bound ADP, d

17 The x-ray crystal structure of tetramethylrhodamine-5-maleimide-actin with bound AMPPNP

18 fluorescein label (6-FAM) and a 3',6-carboxy-tetramethylrhodamine (6-TAMRA) label: 6-FAM-dArUdAdA-6-T

19 yl-lysine residue, with a fluorescent group (tetramethylrhodamine-6-carboxylic acid, 6-TAMRA) near th

20 ed in Xenopus laevis oocytes and tagged with tetramethylrhodamine-6-maleimide (TMR6M).

21 environmentally sensitive fluorescent probe tetramethylrhodamine-6-maleimide (TMRM).

22 laevis oocytes, cysteines were labeled with tetramethylrhodamine-6-maleimide, and voltage-dependent

23 methanethiosulfonate but was inaccessible to tetramethylrhodamine-6-maleimide.

24 ed with fluorescein (a pH-sensitive dye) and tetramethylrhodamine (a pH-insensitive dye), which serve

25 led with either fluorescein (donor probe) or tetramethylrhodamine (acceptor probe) and then used to m

26 ) conjugation of F239C in the large lobe and tetramethylrhodamine (acceptor) conjugation of C343 in t

27 separate pools with fluorescein (donor) and tetramethylrhodamine (acceptor).

28 ubunit tetramethylrhodamine dimers form when tetramethylrhodamine acetamide is attached to two differ

29 f the yeast Bni1p FH2 domain in complex with tetramethylrhodamine-actin.

30 ing of DNA with some fluorescent dyes, e.g., tetramethylrhodamine, alters DNA density on AuNP.

31 nt experiment, dextran (10K) conjugated with tetramethylrhodamine and biotin was injected into the no

32 e N-terminus of mutant LC1, was labeled with tetramethylrhodamine and exchanged into skeletal subfrag

33 f amplified DNA labeled with the fluorophore tetramethylrhodamine and the AP-1 consensus nucleotide s

34 ugated prestin to a photostable fluorophore (tetramethylrhodamine) and performed single-molecule fluo

35 a complementary oligonucleotide labeled with tetramethylrhodamine, and monitored over time for quench

36 was generated, labeled with the fluorophore tetramethylrhodamine, and subjected to various anisotrop

37 able conjugates with biotin, digoxigenin and tetramethylrhodamine are described.

38 luorescein as a pH-dependent fluorophore and tetramethylrhodamine as a pH-independent fluorophore.

39 In this method, Abeta is labeled with tetramethylrhodamine at a lysine residue on the N-termin

40 ulfonic acid at Cys-190 of Tm and phalloidin-tetramethylrhodamine B isothiocyanate bound to F-actin.

41 e peptides that has been labeled with BODIPY-tetramethylrhodamine (BODIPY(TMR)).

42 maleimide and a membrane-impermeant 2-((5(6)-tetramethylrhodamine)carboxylamino) ethyl methanethiosul

43 is of TM1 with biotin maleimide and 2-((5(6)-tetramethylrhodamine)carboxylamino) ethyl methanethiosul

44 tin maleimide (BM)) and impermeant (2-((5(6)-tetramethylrhodamine)carboxylamino)ethyl methanethiosulf

45 s, anterogradely labeled with biotin dextran tetramethylrhodamine, caudal to the lesion.

46 analog of CGP 12177 [bordifluoropyrromethane-tetramethylrhodamine-(+/-)CGP 12177 (BODIPY-TMR-CGP)] at

47 agglutinin-horseradish peroxidase or dextran-tetramethylrhodamine conjugated to biotin.

48 ached to a single cysteine on the serpin and tetramethylrhodamine conjugated to the proteinase.

49 Binding of L7/L12:tetramethylrhodamine cysteine 33 or cysteine 12 dimers e

50 A tetramethylrhodamine derivative of I(A) was prepared and

51 ated cardiac myocytes via photoactivation of tetramethylrhodamine derivatives, which also served to r

52 cells were allowed to endocytose fluorescein tetramethylrhodamine dextran (FRD), a ratiometric probe

53 erent ages received injections of the tracer tetramethylrhodamine dextran (TMR-D) into the nodose gan

54 ganglion cell layer using Nissl staining and tetramethylrhodamine dextran amine backfilling.

55 lus vulgaris leucoagglutinin, Fluoro-Gold or tetramethylrhodamine dextran amine into either the vesti

56 were identified by retrograde labeling with tetramethylrhodamine dextran amine.

57 Tetramethylrhodamine dextran and cholera toxin B uptake

58 ion of a 1.5-microL solution of 0.25% 70-kDa tetramethylrhodamine-dextran (TMR-D).

59 Transscleral permeation by 10-kDa tetramethylrhodamine-dextran also was determined, for co

60 IT-type neurons were retrogradely labeled by tetramethylrhodamine-dextran amine (RDA)3k injection int

61 Transscleral permeation by 10-kDa tetramethylrhodamine-dextran was 1.04 +/- 0.39 x 10(-6)

62 The formation of tetramethylrhodamine dimers caused the appearance of a n

63 The tetramethylrhodamine dimers disappear rapidly (within 5

64 The tetramethylrhodamine dimers do form at sites in the C-te

65 Ground-state tetramethylrhodamine dimers form between the two subunit

66 Intersubunit tetramethylrhodamine dimers form when tetramethylrhodami

67 A fast cleaving non-nucleosidic tetramethylrhodamine dye-labeled support has been develo

68 In hepatocytes loaded with tetramethylrhodamine ethyl ester (10 nM) to quantify mit

69 Tetramethylrhodamine ethyl ester (TMRE) and 2',7'-dichlo

70 ificantly decreased cellular accumulation of tetramethylrhodamine ethyl ester (TMRE) and daunorubicin

71 etramethylrhodamine methyl ester (TMRM), and tetramethylrhodamine ethyl ester (TMRE) as fluorescent p

72 ucose (2-NBDG) reports on glucose uptake and Tetramethylrhodamine ethyl ester (TMRE) reports on mitoc

73 was assessed by flow cytometric analysis of tetramethylrhodamine ethyl ester (TMRE)-loaded cells.

74 nd intact cells using the fluorescent probe, tetramethylrhodamine ethyl ester (TMRE).

75 with a fluorescent Delta(Psi)(m)-indicator, tetramethylrhodamine ethyl ester (TMRE).

76 (m)), as assessed by the potentiometric dye, tetramethylrhodamine ethyl ester (TMRE).

77 ific probe for mitochondrial calcium; and of tetramethylrhodamine ethyl ester fluorescence to monitor

78 ciated with significantly attenuated loss of tetramethylrhodamine ethyl ester fluorescence under basa

79 Consistent with this observation, tetramethylrhodamine ethyl ester perchlorate staining re

80 were monitored using ratiometric pericam and tetramethylrhodamine ethyl ester probe, respectively, to

81 potential (with the potential-sensitive dye tetramethylrhodamine ethyl ester) and in mitochondrial [

82 ous stimuli were assessed by flow cytometry (tetramethylrhodamine ethyl ester).

83 deprivation (OGD) and monitored psi(m) using tetramethylrhodamine ethyl ester.

84 ntial, as monitored by the fluorescent probe tetramethylrhodamine ethyl ester.

85 fluorescence arising from flavoproteins and tetramethylrhodamine ethyl ester.

86 ed with the membrane potential-sensitive dye tetramethylrhodamine-ethyl ester (TMRE) in murine viment

87 drial membrane potential-independent dye and tetramethylrhodamine-ethyl-ester-perchlorate (TMRE) and

88 nd double-stained with MitoTracker Green and tetramethylrhodamine-ethyl-ester-perchlorate were examin

89 in mitochondrial potential as assessed using tetramethylrhodamine ethylester (TMRE).

90 mitochondrial depolarization, assessed using tetramethylrhodamine ethylester, and reactive oxygen spe

91 ssessed by using the potential-sensitive dye tetramethylrhodamine ethylester.

92 ne, phOx) and fluorescent probes (Bodipy Fl, tetramethylrhodamine, fluorescein) were bound with high

93 samine (UDP-GalNAz) that is then linked to a tetramethylrhodamine fluorescent tag and CTD110.6 and RL

94 ear optical calibration curve for 5-carboxyl-tetramethylrhodamine from the concentration detection li

95 ed with a single fluorophore (fluorescein or tetramethylrhodamine) have been used previously as fluor

96 Correlation analysis of Tetramethylrhodamine intensity fluctuations reveals hing

97 The fluorescent probe tetramethylrhodamine iodoacetamide was attached to cyste

98 our DNA nucleotides labeled identically with tetramethylrhodamine is described and demonstrated.

99 orms, fluorescein isothiocyanate (F-ITC) and tetramethylrhodamine isothiocyanate (TR-ITC).

100 rophores (fluorescein isothiocyanate (FITC), tetramethylrhodamine isothiocyanate (TRITC), and carboxy

101 in isothiocyanate dextran (FITC-dextran) and tetramethylrhodamine isothiocyanate concanavalin A (TRIT

102 olecule fluorescence spectroscopy and bear a tetramethylrhodamine isothiocyanate fluorescent tag for

103 The system uses tetramethylrhodamine isothiocyanate labeled asialofetuin

104 Golgi apparatus, BODIPY-ceramide and TRITC (tetramethylrhodamine isothiocyanate)-labeled cholera tox

105 luorescein isothiocyanate (FITC)-dextran and tetramethylrhodamine isothiocyanate-AG encapsulated in m

106 n investigated using two fluorescent probes, tetramethylrhodamine isothiocyanate-labeled phalloidin b

107 r by altering the C terminus of actin with a tetramethylrhodamine label.

108 the fluorescently labeled glycosphingolipid tetramethylrhodamine labeled GM1 (GM1-TMR) produced by s

109 ectrokinetic chromatography separation of 19 tetramethylrhodamine-labeled amino acids was accomplishe

110 as measured by dichroism of 5' iodoacetamido-tetramethylrhodamine-labeled cardiac troponin C.

111 , the measured steady-state polarizations of tetramethylrhodamine-labeled dATP, dCTP, dGTP and dUTP w

112 We report that a tetramethylrhodamine-labeled dimer of the cell-penetrati

113 A tetramethylrhodamine-labeled glycosphingolipid (GM1-TMR)

114 ebella neurons was probed by incubation with tetramethylrhodamine-labeled GM1 (GM1-TMR).

115 elective LPS sensor, developed by assembling tetramethylrhodamine-labeled LPS-binding peptides on gra

116 The binding and unbinding of individual tetramethylrhodamine-labeled neutravidin molecules is me

117 e next correct dNTP; with Klenow polymerase, tetramethylrhodamine-labeled probes increased their fluo

118 Fluorescein- and tetramethylrhodamine-labeled probes of identical sequenc

119 Tetramethylrhodamine-labeled rPfP2 protein exhibited DTT

120 In these measurements, tetramethylrhodamine-labeled, anti-trinitrophenyl IgE an

121 m hydrolyze LacNAc from Galbeta1-4GlcNAcbeta-tetramethylrhodamine (LacNAc-TMR (Galbeta1-4GlcNAcbeta(C

122 hen were incubated with 10 or 70 kDa dextran-tetramethylrhodamine-lysine for 16 to 32 minutes at 37 d

123 re, we labeled the OCP of Synechocystis with tetramethylrhodamine-maleimide (TMR) and obtained a phot

124 Tetramethylrhodamine methyl ester (TMRM) is a fluorescen

125 otential (DeltaPsiP) and the DeltaPsiM probe tetramethylrhodamine methyl ester (TMRM) using fluoresce

126 nvestigated the use of rhodamine 123 (R123), tetramethylrhodamine methyl ester (TMRM), and tetramethy

127 /ml) were incubated in multiwell plates with tetramethylrhodamine methyl ester (TMRM, 1 microM), a po

128 focal microscopy using the fluorescent dyes, tetramethylrhodamine methyl ester and 5,6-carboxy-2',7'-

129 itochondrial membrane potential monitored by tetramethylrhodamine methyl ester decreased abruptly in

130 The fibres were then loaded with the dye tetramethylrhodamine methyl ester perchlorate (TMRM) to

131 , hepatocytes were coloaded with calcein and tetramethylrhodamine methyl ester to visualize onset of

132 The method uses the fluorescent dye tetramethylrhodamine methyl ester, which equilibrates in

133 ement of mitochondrial membrane potential by tetramethylrhodamine methyl ester.

134 on were visualized by confocal microscopy of tetramethylrhodamine methylester (TMRM) and quenching of

135 copy of the potential-indicating fluorophore tetramethylrhodamine methylester (TMRM).

136 axons of chick sensory neurons using the dye tetramethylrhodamine methylester (TMRM).

137 chondrial membrane potential-indicating dye, tetramethylrhodamine methylester.

138 e microcapsules loaded with different loads (tetramethylrhodamine-modified dextran, TMR-D; microperox

139 al deoxynucleotidyltransferase-mediated dUTP-tetramethylrhodamine nick end labeling assay, demonstrat

140 sonance energy transfer donor and anti-actin tetramethylrhodamine phalloidin as an acceptor.

141 For this purpose, Tetramethylrhodamine probes were introduced at pairs of

142 O2 both sensors are chemically converted to tetramethylrhodamine, producing significant (>/=66 nm) b

143 to dextran, together with a red fluorescing tetramethylrhodamine reference chromophore.

144 s were 1 zmol for BODIPY-FL and 500 ymol for tetramethylrhodamine standard solutions.

145 00,000 theoretical plates in 6-14 s for both tetramethylrhodamine succidimidyl ester and fluorescein-

146 ction to simultaneously incorporate an azido-tetramethylrhodamine (TAMRA) fluorophore and an aminooxy

147 ed the zwitterionic, membrane-impermeant dye tetramethylrhodamine (TAMRA) into cells even when the co

148 d 70 kDa dextran, 10 kDa dextran, and 467 Da tetramethylrhodamine (TAMRA) was examined under diffusiv

149 DNA labeled with either fluorescein (FAM) or tetramethylrhodamine (TAMRA) with a metal surface, using

150 In this work fluorescein and tetramethylrhodamine (TAMRA), a Forster resonance energy

151 mparison of Texas Red (TR), fluorescein, and tetramethylrhodamine (TAMRA)-labeled aptamers reveals su

152 A tetramethylrhodamine-Tat conjugate is effectively transl

153 ng either the fluorescein-thiourea (7a-c) or tetramethylrhodamine-thiourea (9a,b) moieties were also

154 Noncovalently "stacked" tetramethylrhodamine (TMR) dimers have been used to both

155 tides labeled at their N-termini with either tetramethylrhodamine (TMR) or 7-nitrobenz-2-oxa-1,3-diaz

156 The fluorescent dye tetramethylrhodamine (TMR) was conjugated to a synthetic

157 it[7]uril (Q7) linked to the fluorescent dye tetramethylrhodamine (TMR), and the characterization of

158 Tetramethylrhodamine (TMR)-doped silica nanoparticles, e

159 ally sensitive fluorescent rhodamines [e.g., tetramethylrhodamine (TMR)-thiols].

160 ed fluorescent Cl(-)-insensitive chromophore tetramethylrhodamine (TMR).

161 beled at its N terminus with the fluorophore tetramethylrhodamine (TMR).

162 s selected to bind a larger fluorescent dye, tetramethylrhodamine (TMR).

163 effectively depolarized by diazoxide (-15%, tetramethylrhodamine [TMRM]), less so by levcromakalim,

164 us using the in vitro application of dextran-tetramethylrhodamine to the pituitary.

165 6-methoxyquinoline and chloride-insensitive tetramethylrhodamine to the zymosan particles.

166 n transport protein transferrin labeled with tetramethylrhodamine undergoes rapid receptor-mediated e

167 of actin made monomeric by modification with tetramethylrhodamine, which show formation of an alpha-h

168 e [(5-(and-6)-((4-chloromethyl)benzoyl)amino)tetramethylrhodamine], which allowed estimation of the g

169 placed the N,N-dimethylamino substituents in tetramethylrhodamine with four-membered azetidine rings.

170 eling on Plk1 and Plk3 targeted by AX7503, a tetramethylrhodamine-wortmannin conjugate.

171 s, biotin-wortmannin, BODIPY-wortmannin, and tetramethylrhodamine-wortmannin.