ライフサイエンスコーパス: acridine orange

1 -dependent acidification was monitored using acridine orange.

2 owing staining with the lysosomotropic agent acridine orange.

3 ence was scored visually after staining with acridine orange.

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

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

6 endocytic vesicles using the fluorescent dye acridine orange.

7 een caffeine and the planar DNA intercalator acridine orange.

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

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

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

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

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

13 ative to measuring chromatin condensation by acridine orange analysis.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

56 When acridine orange fluorescence quenching was used to measu

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

77 10-N-Nonyl acridine orange (NAO) is widely used to image CL in bact

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

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

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

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

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

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

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

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

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

87 An FC procedure using acridine orange provided minimum inhibitory concentratio

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

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

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

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

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

93 Studies with acridine orange stain demonstrated that the majority of

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

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

96 Acridine orange staining of EDL-155-treated retinoblasto

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

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

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

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

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

102 Acridine orange staining, which distinguishes cells in G

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

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

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

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

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

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

109 Measurements of acridine orange uptake in permeabilized procyclic trypom

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

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

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

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

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