ライフサイエンスコーパス: acridine orange

1 een caffeine and the planar DNA intercalator acridine orange.

2 sma treated cells that stained positive with acridine orange.

3 -dependent acidification was monitored using acridine orange.

4 owing staining with the lysosomotropic agent acridine orange.

5 ence was scored visually after staining with acridine orange.

6 ty, after staining with propidium iodide and acridine orange.

7 the mitochondrion-selective probe, 10-nonyl acridine orange.

8 endocytic vesicles using the fluorescent dye acridine orange.

9 pyl]-6-phenylphenanthridinium diiodide), and acridine orange (3,6-bis(dimethylamino)acridinium chlori

10 The triplet excited state of acridine orange ((3)*AO) undergoes a proton-coupled elec

11 The motile vesicles accumulated the dye acridine orange, a marker for endosomes and lysosomes.

12 tion (Deltapsi), and quantitative culture or acridine orange accumulation was used to measure viabili

13 Nondenaturing gels stained with acridine orange, after incubation in ADP, reveal that th

14 ative to measuring chromatin condensation by acridine orange analysis.

15 visualization of chromatin fragmentation by acridine orange and 4'6-diamidino-2-phenylindole stainin

16 After 1 hour, cells were stained with acridine orange and assessed by confocal laser-scanning

17 The use of acridine orange and dextran-tagged dyes as probes for th

18 PMNL were stained with acridine orange and ethidium bromide after 0, 3, 6, and

19 Further studies using acridine orange and ethidium bromide to measure apoptosi

20 escence microscopy (after cell staining with acridine orange and ethidium bromide).

21 alyzed for mitochondrial content using nonyl acridine orange and function using rhodamine 123.

22 using rapid extrinsic nuclear staining with acridine orange and intrinsic second harmonic contrast g

23 nalysis using the mitochondrial probes nonyl-acridine orange and JC-1 confirmed a progressive increas

24 EDL-155-treated Y79-Luc cells, staining with acridine orange and LC-3 immunoblot analysis was perform

25 ular Probes, Eugene, OR), lysosomal content (acridine orange and Lysotracker Red [Invitrogen-Molecula

26 Instead, staining with acridine orange and microtubule-associated protein 1 lig

27 In these experiments, HGF were stained with acridine orange and quantified per unit area of dentin b

28 ell nuclei become permeable to the vital dye acridine orange and their DNA undergoes fragmentation, i

29 ron microscopy (SEM) as well as alamar blue, acridine orange, and alizarin red assays.

30 viability was examined with ethidium bromide-acridine orange, and apoptosis was examined using a quan

31 Cells were then stained with acridine orange, and apoptotic indices were calculated a

32 To accomplish this, acridine orange (AO) histofluorescence was employed, alo

33 al fluorescence microscopy, the pH indicator acridine orange (AO) identified intense fluorescence sta

34 k-end labeling (TUNEL) for fixed tissues and acridine orange (AO) staining for live embryos or tissue

35 triggered secretion from astrocytes, we used acridine orange (AO) to label vesicles.

36 In this study, an organic dye acridine orange (AO) was successfully loaded on the LDH

37 The photosensitizers rose bengal (RB) and acridine orange (AO) were localized to the plasmalemma a

38 Acridine orange (AO), a nucleic acid dye with unique spe

39 Fluorescence of acridine orange (AO), which selectively sequesters into

40 d by its acquisition of the acidotropic base acridine orange (AO).

41 oxoxanthine) with the known DNA intercalator acridine orange (AO).

42 hylene blue [MB]) or to study P. falciparum (acridine orange [AO]).

43 d on selective ternary complex of As(V) with acridine orange (AOH(+)) being a versatile fluorescence

44 slet cells stained with ethidium bromide and acridine orange, apoptosis using a quantitative kit, NF-

45 aic images of prostate biopsies stained with acridine orange are rendered in seconds and contain exce

46 borated protocol highlights the use of nonyl acridine orange as a photocatalyst to generate a sulfeny

47 ever, a cardiolipin-specific dye, 10-N-nonyl acridine orange, could preferentially suppress Bid bindi

48 and distamycin and the intercalating ligand acridine orange destabilize the (TTC)6.(GAA)6 composite

49 nded DNA based on differential staining with acridine orange, DNase I sensitivity, electrophoretic mo

50 nO(3) nanocomposites for photodegradation of Acridine orange dye (AO) was evaluated over visible ligh

51 cope after immersion in a 0.6 mM solution of acridine orange dye for 10-20 seconds.

52 DNA fragmentation and ethidium bromide/acridine orange (EB/AO) nuclear staining were performed

53 Staining with the lysosomotropic agent acridine orange enabled us to quantify AVO accumulation

54 We evaluated the potential of several dyes [acridine orange, ethidium bromide, ethidium homodimer, b

55 Further, acridine orange, ethidium bromide, propidium iodide and

56 triggered MM cell apoptosis as evidenced by acridine orange-ethidium bromide staining.

57 udied by cell morphology, DNA fragmentation, acridine orange/ethidium bromide (AO/EB) staining, cell

58 poptosis as detected by staining with either acridine orange/ethidium bromide or annexin-V-fluorescei

59 c criteria: green to orange/yellow shifts on acridine orange/ethidium bromide staining, and cell surf

60 well as by assessment of DMP 777 effects on acridine orange fluorescence and H(+),K(+)-adenosine tri

61 When acridine orange fluorescence quenching was used to measu

62 easured by the extent of succinate-dependent acridine orange fluorescence quenching, but increased so

63 be assayed for ATP-dependent H+ transport by acridine orange fluorescence quenching, none showed an a

64 elevated number (15% increase in mean nonyl acridine orange fluorescence) of dysfunctional mitochond

65 As assayed by changes in acridine orange fluorescence, imposing an outwardly dire

66 n, and abolished proton pumping as probed by acridine orange fluorescence.

67 Salt resistance assays, acridine-orange fluorescence dequenching, solid supporte

68 t 24 hpf through staining with the vital dye acridine orange, followed by counting the stained cells

69 ultaneous fluorescence imaging of release of acridine orange from individual vesicles confirmed the e

70 s were smaller and in higher number, showing acridine orange green fluorescence emission, which corro

71 ] > Ru(bpy)(3)(2+) [bpy = 2,2'-bipyridine] > acridine orange > ethidium, in accordance with measured

72 ed the distribution of the fluorescent amine acridine orange in activated sludge by confocal fluoresc

73 an increased amount of DNA intercalation by acridine orange in PARG null-TS cells.

74 ive, activate caspase-3 and are positive for acridine orange, indicating they undergo apoptosis.

75 e acidic pH, as they exclude LysoTracker and acridine orange; inhibiting the V-ATPase with bafilomyci

76 Acridine orange intensity correlates closely with the ly

77 hiocyanate-coupled concanavalin A lectin and acridine orange labeling.

78 ed the signal collection from the nucleus of Acridine orange labelled human fibroblast cells, the nuc

79 The gram stain and acridine-orange leucocyte cytospin test (AOLC) is rapid

80 lture (Q* = 0.89 [CI, 0.79 to 0.99]) and the acridine orange leukocyte cytospin test (Q* = 0.89 [CI,

81 inal leukocyte adhesion was quantitated with acridine orange leukocyte fluorography.

82 either by staining with an ethidium bromide/acridine orange mixture (AO/EB) or with Annexin V-phycoe

83 the mitochondrial-specific probe 10-N-nonyl acridine orange (NAO) are injected into a fused-silica c

84 ications using the mitochondrial probe nonyl acridine orange (NAO) indicated that initial increases i

85 Nonyl-acridine orange (NAO) is a specific probe of cardiolipin

86 10-N-Nonyl acridine orange (NAO) is widely used to image CL in bact

87 pin (CL)-specific fluorescent dye 10-N-nonyl-acridine orange (NAO) was used to visualize CL distribut

88 scle cross section was stained with 10-nonyl acridine orange (NAO) which is a mitochondrion-selective

89 uorescent polystyrene particles and 10-nonyl acridine orange (NAO)-labeled mitochondria were used as

90 mined by DNA fragmentation, ethidium bromide-acridine orange nuclear stain and TdT-mediated dUTP nick

91 that complex formation between caffeine and acridine orange or ethidium bromide results in singlet-s

92 zinc is acidic as revealed by staining with acridine orange or LysoTracker.

93 by photoactive Lewis basic molecules such as acridine orange or naphthalene-fused N-acylbenzimidazole

94 ificant fluorescence spectral alterations in acridine orange, perhaps because of thermally induced DN

95 abnormal muscle fibers of IBM contained (i) acridine-orange-positive RNA inclusions that colocalized

96 om the exogenous fluorescent probes laurdan, acridine orange, propidium iodide, and Snarf are used to

97 An FC procedure using acridine orange provided minimum inhibitory concentratio

98 meabilization was monitored using uptake and acridine orange relocation techniques.

99 e fluorescent dyes dihydroethidine and nonyl-acridine orange, respectively.

100 Staining with 10-N-nonyl-acridine orange revealed a single microdomain enriched w

101 Staining with the fluorescent dye 10-N-nonyl acridine orange revealed anionic phospholipid membrane d

102 -infected hamsters using the fluorescent dye acridine orange revealed that RNA molecules co-localize

103 Studies with acridine orange stain demonstrated that the majority of

104 Aerobic BACTEC broths received an acridine orange stain on day 8 and were subcultured at 2

105 their capacity to induce apoptosis, using an acridine orange staining assay.

106 Acridine orange staining of EDL-155-treated retinoblasto

107 Using annexin V and acridine orange staining techniques, macrophages phagocy

108 Annexin V, propidium iodide, and acridine orange staining were measured by flow cytometry

109 ery (VCR) with trypan blue, ethidium bromide/acridine orange staining, and terminal deoxynucleotidyl

110 cal (histology, nuclear morphology following acridine orange staining, electron microscopy) and bioch

111 c lung fibroblasts in vitro, as evidenced by acridine orange staining, terminal transferase nick end

112 Acridine orange staining, which distinguishes cells in G

113 usion from both ears of both mouse groups by acridine orange staining.

114 immunoblotting, GFP-LC3 relocalization, and acridine orange staining.

115 Gram, Giemsa, calcofluor white, and acridine orange stains and electron microscopy showed no

116 e assayed as reconstituted vesicles by using acridine orange to indicate ATP-dependent hydrogen ion t

117 e redistribution of the lysosomal tropic dye acridine orange to the cytosol, and the triggering of ap

118 rdiac cycle, were recorded after infusion of acridine orange (to fluorescently label leukocytes) duri

119 Measurements of acridine orange uptake in permeabilized procyclic trypom

120 ane HCl transport, assessed by ATP-dependent acridine orange uptake, was unaffected by 17-beta-estrad

121 igotes of Trypanosoma brucei, as measured by acridine orange uptake.

122 n exteriorized ileal segment and FITC-BSA or acridine orange was used to quantitate macromolecular le

123 Sperm labeled with acridine orange were analyzed by flow cytometry to measu

124 oanilino)-3'-amino-N-methyldipropylamine and acridine orange were not localized to either inclusion t

125 ary mouse model of sarcoma were stained with acridine orange, which stains cell nuclei, skeletal musc