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1 displayed additional direct competition with phenol red.
2 d by a contaminant (1) present in commercial phenol red.
4 yses in the presence of the pH indicator dye phenol red, along with studies of the pH dependence of o
5 urther free energy analysis suggested that a phenol red analog may potentially improve the binding af
6 etection is decreased by a factor of 7.2 for phenol red and a factor of 3.3 for nanoparticles and dye
7 n of an ammonia-sensitive absorbing reagent (phenol red) and an analyte-insensitive fluorophore (rhod
8 abeled derivatives of phenolsulfonphthalein (phenol red) and meta-cresolsulfonphthalein (cresol purpl
9 ture medium in solution showed that glucose, phenol red, and amino acids all acted to detoxify or rem
10 ns from the lipophilic impurities present in phenol red, and we determined the structure of two activ
12 digitoxin as probes for the digitoxin site, phenol red as a probe for the bilirubin site, and cisor
13 ensitive dyes (carboxyfluorescein at pH 6.5, phenol red at pH 7.5, and m-cresol purple at pH 8.5) whi
15 y evaluates the use of hydroxynaphthol blue, phenol red, calcein, leuco crystal violet, malachite gre
18 g the hydrogen bond direction indicates that phenol red does not directly block the beta-sheet extens
21 rred 24 h before the start of experiments to phenol red-free and FBS-free media to minimize exogenous
22 ndothelial cells (HUVECs) were propagated in phenol red-free gonadal hormone-free medium and pretreat
23 xity in male hippocampal neurons cultured in phenol red-free media or in the presence of an estrogen
25 iol, or 100 nM tamoxifen or dexamethasone in phenol red-free, serum-free medium to measure the steady
26 man gingival fibroblasts (GF) were tested in phenol red-free, serum-free medium with or without the p
32 using rapid kinetics and the H(+) indicator phenol red in solutions weakly buffered by substrate L-s
33 tion of absorbance change of a pH indicator, phenol red, in response to proton release that accompani
34 isothermal amplification technique using the phenol red indicator (QLAMP-PhR) for detecting Fusobacte
35 ferences unique to cell culture, such as the phenol red indicator dye used in most cell culture media
36 and utilized with master mix reagents, and a phenol red indicator was employed to enhance the QLAMP-P
37 +/- 2 ml/min to 23 +/- 2 ml/min when KoA for phenol red, KoAPR, was increased from 238 to 640 ml/min
38 o a non-nutrient meal was measured using the phenol red method and pyloric function was assessed by m
42 ying, as assessed following an oral bolus of phenol red or independently by [(99m)Tc]-diethylenetriam
48 ore and after the exposure: tear osmolarity, phenol red thread test, conjunctival hyperemia, fluoresc
49 before and after exposure: tear osmolarity, phenol red thread test, conjunctival hyperemia, fluoresc
50 tear film (e.g., interferometry, osmolality, phenol red thread, meibography, fluorescein, and lissami
53 nd methyltetrahydrofolate in the presence of phenol red, we show that this proton uptake occurs at a
55 ly converted TBBPA to bisphenol A and BPB to phenol red with a stepwise removal of all bromide substi