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1 copy using 2',7'-bis(2-carboxyethyl)-5-(and -6)carboxyfluorescein.
2 of RhB in intralipid and to measure pH using 6-carboxyfluorescein.
3 ive fluorescent dye 2'7'-bis(carboxyethyl)5-(6)-carboxyfluorescein.
4 pH-sensitive dye 2',7'-bis(2-carboxyethyl)-5(6)-carboxyfluorescein.
5 zITP filter was used to enhance detection of 6-carboxyfluorescein 4-fold over fluorescein, even thoug
7 usion coefficient of four different dyes, 5-(6)-carboxyfluorescein, 5-chloromethylfluorescein, Oregon
8 K) organ culture systems was developed using 6-carboxyfluorescein, 5-carboxyfluorescein, and fluoresc
9 hepatocytes into its fluorescent derivative 6-carboxyfluorescein (6-CF) and secreted into the canali
10 n's axon in the living leech was filled with 6-carboxyfluorescein (6-CF) dye and cut with an argon la
12 sing guanine (G)-rich DNA aptamer-conjugated 6-carboxyfluorescein (6-FAM) capable of rapidly capturin
13 splaying optimal performance was composed of 6-carboxyfluorescein (6-FAM) on the peptide N-terminus,
14 Similar results were obtained with 5-(and-6)-carboxyfluorescein-6-aminohexyl ouabain as acceptor.
15 -diazol-4-yl]-6-aminohexyl ouabain or 5-(and-6)-carboxyfluorescein-6-aminohexyl ouabain bound to the
16 owing donor/acceptor pairs were synthesized: 6-carboxyfluorescein/6-carboxy-X-rhodamine (FAM-ROX), 3-
17 are oligonucleotides with a 5' reporter dye (6-carboxyfluorescein), a quencher dye (6-carboxy-tetrame
18 based on the inhibition of the transport of 6-carboxyfluorescein, a high-affinity hOAT1 substrate (K
19 measured with 2',7'-bis(carboxyethyl)-S-(and 6)carboxyfluorescein acetoxy methylester/fluorometry.
21 d a probe, 2',7'-bis-(2-carboxyethyl)-5-(and-6)-carboxyfluorescein acetoxymethyl ester (BCECF-AM), th
22 indicator 2',7'-bis-(2-carboxyethyl)-5-(and-6)-carboxyfluorescein-acetoxymethyl ester, the initial r
24 luorescent probe 2',7'-bis(2-carboxyethyl)-5,6-carboxyfluorescein-acetoxymethyl ester was used to qua
25 excitation ratio of 2,7-bis(carboxyethyl)-5(6)-carboxyfluorescein and calibrated with nigericin and
26 with the pH probe 2',7'-bis(carboxyethyl)-5(6)-carboxyfluorescein and mounted in a bilateral perfusi
27 d sensing was demonstrated using mixtures of 6-carboxyfluorescein and [Ru 2,2'-(bipyridyl)3]2+ as a p
28 ha-thrombin binding aptamer was labeled with 6-carboxyfluorescein and exploited as a selective fluore
29 -based sensing was demonstrated for pH using 6-carboxyfluorescein and for protein affinity or immunoa
30 nsitive indicator 2',7'-bis(carboxyethyl)-5-(6)-carboxyfluorescein, and Na+ transport was measured un
31 lity of the complex of wild-type RNase A and 6-carboxyfluorescein approximately d(AUAA) at varying pH
32 decreases the stability of the complex with 6-carboxyfluorescein approximately d(AUAA) by 2.3 kcal/m
33 s determined with the fluorogenic substrate: 6-carboxyfluorescein approximately dArXdAdA approximatel
34 ptake were correlated with molecular size: 5(6)-carboxyfluorescein (approximately 32%), 7-hydroxycoum
35 known hOAT1 substrates determined using the 6-carboxyfluorescein-based inhibition assay correlated w
36 ter using 2',7'-bis-(2-carboxyethyl)-5-(and -6)-carboxyfluorescein (BCECF) as a cytoplasmic pH indica
38 ensitive dye 2',7'-bis-(carboxyethyl)-5-(and-6)-carboxyfluorescein (BCECF) indicated that previous K(
39 itive fluoroprobe 2'7'-bis(2-carboxyethyl)-5(6)-carboxyfluorescein (BCECF) or the sodium-binding benz
40 rescein derivative 2,7-bis(2-carboxyethyl)-5(6)-carboxyfluorescein (BCECF) was monitored by high-thro
41 dicated by 2',7'-Bis-(2-Carboxyethyl)-5-(and-6)-carboxyfluorescein (BCECF), a pH sensitive fluorescen
42 ymethyl of 2',7'-bis-(2-carboxyethyl)-5-(and 6)-carboxyfluorescein (BCECF), BCECF conjugated to 70-kD
43 assessed by 2',7'-bis(2-carboxyethyl)-5-(and-6)-carboxyfluorescein (BCECF), Fura-2 and differential i
44 helium performed with 2',7-biscarboxyethyl-5(6)-carboxyfluorescein (BCECF), the selective V-ATPase in
45 sitive dye, 2',7'-bis(2-carboxyethyl)-5-(and-6)-carboxyfluorescein (BCECF), were coated onto the prob
46 re used is 2',7'-bis-(2-carboxyethyl)-5-(and-6)-carboxyfluorescein (BCECF), whose lifetime tau (pH 4.
47 copy with 1',7'- bis-(2-carboxyethyl)-5-(and-6)-carboxyfluorescein (BCECF)-dextran demonstrated that
56 ator dye 2', 7'-bis-(2-carboxyethyl)-5-(and -6)carboxyfluorescein (BCECF) is routinely used to measur
57 dominal aorta, using 2',7'-biscarboxyethyl-5(6)carboxyfluorescein (BCECF) on a microscope-based fluor
58 luorescent probes, 2',7'-bis(carboxyethyl)-5,6-carboxyfluorescein (BCECF) and fura-2, respectively.
59 CO(2)/HCO(3)(-) by 2',7'-bis(carboxyethyl)-5,6-carboxyfluorescein (BCECF) fluorometry of stably slc4a
60 ratio imaging with 2',7'-bis(carboxyethyl)-5,6-carboxyfluorescein (BCECF) or sodium-binding benzofura
61 ve fluorescent dye 2',7'-bis(carboxyethyl)-5,6-carboxyfluorescein (BCECF) to study the regulation of
62 ric monitoring of 2',7'-bis(carboxyethyl)-5, 6-carboxyfluorescein (BCECF), to assess changes in pHi o
64 or (pyranin or [2',7'-bis (2-carboxyethyl)-5(6)-carboxyfluorescein] [BCECF]) was trapped in egg phosp
65 s 5' labeled with fluorescent probes such as 6-carboxyfluorescein can be rapidly separated and quanti
66 nding of the fluorescent polyanionic probe 5(6)-carboxyfluorescein (CF) to various generations of den
67 tion by utilizing a pH sensitive dye, 5-(and-6)-carboxyfluorescein, conjugated to free lysine residue
68 cterized, each containing a fluorescent dye (6-carboxyfluorescein) connected to the 5' end via a phot
69 pH-indicator 2,7-bis-(2-carboxyethyl)-5-(and-6)-carboxyfluorescein corroborated these changes in pH(c
70 luminal binding dye molecules such as 5-(and-6)-carboxyfluorescein diacetate succinimidyl ester (CFDA
71 ntracellular fluorescent marker CFSE (5-(and-6)-carboxyfluorescein diacetate succinimidyl ester) to t
72 the amine-reactive fluorescent label, 5-(and-6)-Carboxyfluorescein Diacetate Succinimidyl Ester, and
73 an FITC-based membrane-binding dye, 5-(and -6)-carboxyfluorescein diacetate succinimidyl ester, to a
75 y to recruit adoptively transferred 5- (and -6)-carboxyfluorescein diacetate succinimidyl ester-label
76 (5-bromo-2'-deoxyuridine)- and CFSE [5-(and 6)-carboxyfluorescein diacetate succinimidyl ester]-labe
77 by collagenase perfusion and labeled using 5(6)-carboxyfluorescein diacetate succinimidyl-ester (CMFS
78 have found that sorted CFSE(bright) (5-(and-6)-carboxyfluorescein diacetate succinmidyl ester) (nond
79 reshly isolated NK cells labeled with 5-(and-6)-carboxyfluorescein diacetate, succinimidyl ester (CFS
80 ormal CD34(+) cells were labeled with 5-(and 6-)-carboxyfluorescein diacetate succinimidyl ester (CFS
83 oscopy to quantify the transport kinetics of 6-carboxyfluorescein diacetate (6-CFDA), which is proces
84 able intracytoplasmic fluorescent dye 5- and 6-carboxyfluorescein diacetate succinimidyl ester and br
86 de (GO) as quencher, where an amino and FAM (6-carboxyfluorescein) dual labeled DNA was covalently at
87 oline) bilayer vesicles encapsulating 5-(and-6)-carboxyfluorescein dye showed that apoE4 remodeled an
89 ces), and (iv) the dyes chosen as the donor (6-carboxyfluorescein, F; or 3-(epsilon-carboxypentyl)-3'
90 y" 1,3-dipolar cycloaddition between alkynyl 6-carboxyfluorescein (FAM) and azido-labeled single-stra
94 Atto488 (emitting at the same wavelength as 6-carboxyfluorescein, FAM) and Atto467N (emitting at the
95 llowed by monitoring the fluorescence from a 6-carboxyfluorescein (FAM6) fluorophore covalently linke
96 nt cells and by 2'-7'-bis[2-carboxymethyl]-5(6)-carboxyfluorescein fluorescence measuring the acceler
97 for West Nile virus (WNV) detection using a 6-carboxyfluorescein fluorophore and TaqMan for internal
98 ere labeled with different fluorescent dyes (6-carboxyfluorescein for gG2 and 6-hexachlorofluorescein
99 was demonstrated by the cellular uptake of 5(6)-carboxyfluorescein from the culture medium when extra
101 e dye BCECF [2',7'-bis-(carboxyethyl)-5-(and-6)-carboxyfluorescein] in wide-field and confocal micros
102 pH-sensitive dye 2', 7'-bis(carboxyethyl)-5(6)-carboxyfluorescein; intracellular pH (pHi) was measur
103 rescent dye 4',5'-dichloro-2',7'-dimethoxy-5(6)-carboxyfluorescein (JOE) is reported; the overall yie
104 mal substrate is a tetranucleotide with a 5',6-carboxyfluorescein label (6-FAM) and a 3',6-carboxy-te
106 a single multiplex PCR while incorporating a 6-carboxyfluorescein-labeled universal primer to fluores
107 (NASBA-ECL assay) and a real-time assay with 6-carboxyfluorescein-labeled virus-specific molecular be
108 he fluorescent dye 2'-7'-bis(carboxyethyl)-5,6-carboxyfluorescein so that changes in intracellular pH
110 V-6A induces cell division, as measured by 5,6-carboxyfluorescein succinimidyl ester dye and flow cyt
111 and response of 2', 7'-bis(2-carboxyethyl)-5(6)-carboxyfluorescein to H+ were the same in all cell li
112 icated that the proximity of the chromophore 6-carboxyfluorescein to the 2-nitrobenzyl linker did not
113 ds] at the 5' end with 4,7,2',7'-tetrachloro-6-carboxyfluorescein) using HaeIII and BstEII and of a 4
115 BCECF (1,2',7'-bis(2-carboxyethyl)-5-(and -6-)-carboxyfluorescein) was included in microinjectate,