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