ライフサイエンスコーパス: phenol red

1 displayed additional direct competition with phenol red.

2 d by a contaminant (1) present in commercial phenol red.

3 Here, it is applied to the detection of phenol red, 10 nm gold nanoparticles, and envy green flu

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

11 Trypan blue and phenol red are used as examples of synthetic dyes, and r

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

14 ClPR from values of Qp, Qd, the fraction of phenol red bound to albumin (94% +/- 1%) and KoAPR.

15 The clearance of phenol red (ClPR) was compared with the clearances of ur

16 However, phenol red did bind at the warfarin-azapropazone site of

17 g the hydrogen bond direction indicates that phenol red does not directly block the beta-sheet extens

18 -2-oleoyl-phosphocholine inhibits leakage of phenol red dye from liposomes.

19 Phenol red exhibits modest inhibition toward fibril form

20 ndothelial cells (HUVECs) were propagated in phenol red-free gonadal hormone-free medium and pretreat

21 xity in male hippocampal neurons cultured in phenol red-free media or in the presence of an estrogen

22 uction were measured in vitro in serum-free, phenol red-free medium.

23 iol, or 100 nM tamoxifen or dexamethasone in phenol red-free, serum-free medium to measure the steady

24 man gingival fibroblasts (GF) were tested in phenol red-free, serum-free medium with or without the p

25 In preliminary experiments using a phenol red gavage technique in fasted SD rats, we showed

26 Aqueous tear production was measured using phenol red-impregnated cotton threads.

27 Tear production was measured with phenol red-impregnated cotton threads.

28 Thus, phenol red improves the solubility of the early protofib

29 using rapid kinetics and the H(+) indicator phenol red in solutions weakly buffered by substrate L-s

30 tion of absorbance change of a pH indicator, phenol red, in response to proton release that accompani

31 ferences unique to cell culture, such as the phenol red indicator dye used in most cell culture media

32 +/- 2 ml/min to 23 +/- 2 ml/min when KoA for phenol red, KoAPR, was increased from 238 to 640 ml/min

33 o a non-nutrient meal was measured using the phenol red method and pyloric function was assessed by m

34 Through its three aromatic rings, the phenol red molecule preferentially interacted with the h

35 The binding of phenol red molecules to the protofibrils of an amyloidog

36 The phenol red molecules were observed to bind primarily alo

37 mercial preparations of the pH indicator dye phenol red (phenolsulfonphthalein).

38 Phenol red stimulated growth (p<0.001), but channel modu

39 ore and after the exposure: tear osmolarity, phenol red thread test, conjunctival hyperemia, fluoresc

40 before and after exposure: tear osmolarity, phenol red thread test, conjunctival hyperemia, fluoresc

41 tear film (e.g., interferometry, osmolality, phenol red thread, meibography, fluorescein, and lissami

42 us was evaluated with tear production with a phenol-red thread method.

43 Phenol red was given by gavage 100 minutes after anesthe

44 nd methyltetrahydrofolate in the presence of phenol red, we show that this proton uptake occurs at a

45 Clearance values for phenol red were much lower than clearance values for the

46 ly converted TBBPA to bisphenol A and BPB to phenol red with a stepwise removal of all bromide substi