ライフサイエンスコーパス: diamidino

1 in this investigation clearly show that 4,6-diamidino-2 phenylindole (DAPI) is superior to both of t

2 d to study the excited triplet state of 4',6-diamidino-2-phenyl indole (DAPI) and its complexes with

3 t images of the chromosomes stained with 4,6-diamidino-2-phenylindole (DAPI) [5].

4 d for intracapsid steric restriction of 4',6-diamidino-2-phenylindole (DAPI) binding to packaged DNA.

5 Staining with 4',6-diamidino-2-phenylindole (DAPI) indicated that poly- pho

6 show that the ICD of minor-groove-bound 4',6-diamidino-2-phenylindole (DAPI) originates from an intri

7 nd labeling (TUNEL) in conjunction with 4'6'-diamidino-2-phenylindole (DAPI) staining and by fluoresc

8 agnetic resonance imaging, mCherry with 4',6-diamidino-2-phenylindole (DAPI) staining and green fluor

9 assessment of nuclear fragmentation by 4, 6-diamidino-2-phenylindole (DAPI) staining.

10 ter combined propidium iodide (PI) and 4', 6-diamidino-2-phenylindole (DAPI) staining.

11 6-Diamidino-2-phenylindole (DAPI) was used for nuclear cou

12 groove binding compounds, netropsin and 4,6-diamidino-2-phenylindole (DAPI), and a DNA hairpin havin

13 ell extracts, and staining of cells with 4,6-diamidino-2-phenylindole (DAPI), and the polyP-binding d

14 ng toxin (Cdt), connective tissue (CT), 4',6-diamidino-2-phenylindole (DAPI), human gingival epitheli

15 cytolethal distending toxin (Cdt), 4',6-diamidino-2-phenylindole (DAPI), human gingival epitheli

16 microscope after labeling in vitro with 4',6-diamidino-2-phenylindole (DAPI), intracellular injection

17 4',6-diamidino-2-phenylindole (DAPI), netropsin, and pentamid

18 ei frequently do not stain equally with 4',6-diamidino-2-phenylindole (DAPI), suggesting that byr4 is

19 finity exhibited by 5PTB, netropsin and 4',6-diamidino-2-phenylindole (DAPI), two AT-specific minor g

20 ibuprofen (IBU), fluorescein (FLU), and 4',6-diamidino-2-phenylindole (DAPI), was achieved with this

21 ent of changes in the fluorescence of a 4',6-diamidino-2-phenylindole (DAPI)-dsDNA complex upon RecA

22 based on changes in the fluorescence of 4',6-diamidino-2-phenylindole (DAPI)-dsDNA complexes.

23 Two types of foci have been defined: 4,6-diamidino-2-phenylindole (DAPI)-sensitive foci that are

24 harged dyes, propidium iodide (PrI) and 4'-6-diamidino-2-phenylindole (DAPI).

25 a fluorescent DNA minor groove binder, 4',6-diamidino-2-phenylindole (DAPI).

26 nd with the minor groove binding ligand 4',6-diamidino-2-phenylindole (DAPI).

27 crophages were stained with the DNA dye 4',6-diamidino-2-phenylindole (DAPI).

28 n the method: TO-PRO-3 iodide (TP3) and 4',6-diamidino-2-phenylindole (DAPI).

29 hods: staining intact chloroplasts with 4',6-diamidino-2-phenylindole (DAPI); staining at the single-

30 romosome probes, single-copy genes, and 4'-6-diamidino-2-phenylindole (DAPI-) and G-banded chromosome

31 l level using double immunostaining plus 4,6-diamidino-2-phenylindole (for nuclei) counterstaining.

32 on of polyP in the dense granules using 4',6-diamidino-2-phenylindole and by its release together wit

33 ng with anti-alpha-tubulin antibody and 4',6-diamidino-2-phenylindole and flow cytometric analysis of

34 tochemical staining of cellular DNA with 4,6-diamidino-2-phenylindole demonstrated TNF-alpha-induced

35 ive fluorescent reagents SYPRO Ruby and 4',6-diamidino-2-phenylindole dihydrochloride (DAPI), to dete

36 Apoptosis was evaluated by 4',6-diamidino-2-phenylindole dihydrochloride and terminal de

37 kit and of dead (apoptotic) cells using 4',6-diamidino-2-phenylindole dihydrochloride nuclear stainin

38 cent dye molecules per CPMV using DAPI (4',6-diamidino-2-phenylindole dihydrochloride), propidium iod

39 thermore, microtubule immunostaining and 4,6-diamidino-2-phenylindole DNA staining demonstrated that

40 These cells were later stained with 4', 6-diamidino-2-phenylindole for simultaneous DNA analysis a

41 ate nuclear localization correlated with 4,6-diamidino-2-phenylindole light regions and is excluded f

42 sed by trypan blue exclusion assays and 4',6-diamidino-2-phenylindole nuclear staining.

43 specific probes, in addition to inverted 4,6-diamidino-2-phenylindole or conventional G-banding analy

44 xed permeabilized red blood cells with 4',6'-diamidino-2-phenylindole or YOYO-1, a sensitive nucleic

45 rast microscopy, and in selected cases 4',6'-diamidino-2-phenylindole staining and DNA fragmentation.

46 4',6'-diamidino-2-phenylindole staining demonstrated that ther

47 We also used 4',6-diamidino-2-phenylindole staining of isolated plastids t

48 was developed based on the patterns of 4',6-diamidino-2-phenylindole staining of the Nipponbare pach

49 bution of the actin cytoskeleton, DNA (4', 6-diamidino-2-phenylindole staining), and calcofluor-stain

50 tin fragmentation by acridine orange and 4'6-diamidino-2-phenylindole staining, and (3) agarose gel e

51 ic, as assessed by Annexin V staining, 4',6'-diamidino-2-phenylindole staining, and DNA fragment ELIS

52 ediated dUTP nick-end labeling (TUNEL), 4',6-diamidino-2-phenylindole staining, and immunohistochemis

53 hanges in nuclear morphology detected by 4,6-diamidino-2-phenylindole staining, DNA fragmentation ass

54 c apoptotic changes, as demonstrated by 4',6-diamidino-2-phenylindole staining, lack of either DNA la

55 localized to the contractile vacuole by 4',6-diamidino-2-phenylindole staining, suggesting, with the

56 by caspase-3 activity assay, TUNEL, and 4',6-diamidino-2-phenylindole staining.

57 combination of chromosome painting and 4',6-diamidino-2-phenylindole staining.

58 ium surfaces were measured according to 4'-6-diamidino-2-phenylindole staining.

59 e for cytokeratins 8, 18, and/or 19 and 4',6-diamidino-2-phenylindole were considered to be CTCs.

60 eading to H3.3 deposition on H3K9me3(+)/4',6-diamidino-2-phenylindole(+) heterochromatin nuclear foci

61 DAPI (4,6-diamidino-2-phenylindole) inhibited the assembly of a hi

62 DAPI (4',6'-diamidino-2-phenylindole) staining of the arrested cells

63 ragmentation of cellular DNA, and DAPI (4',6-diamidino-2-phenylindole) staining revealed condensation

64 Also, DAPI (4',6'-diamidino-2-phenylindole) staining revealed that chromos

65 uridine (BrdU) pulse-labeling and DAPI (4',6-diamidino-2-phenylindole) staining, which precisely esta

66 escent foci that colocalize with DAPI (4',6'-diamidino-2-phenylindole)-positive material and follow D

67 ctivation of the channel by diminazene, 4',6-diamidino-2-phenylindole, and pentamidine, examine sever

68 e peptide gramicidin, and a DNA-ligand (4',6-diamidino-2-phenylindole, DAPI) system in this work high

69 Microbes were enumerated by 4',6-diamidino-2-phenylindole, dihydrochloride (DAPI) stainin

70 s stained with propidium iodide (PI) or 4',6-diamidino-2-phenylindole, dihydrochloride (DAPI).

71 Using the nucleus-specific stain 4',6-diamidino-2-phenylindole, nuclear fragmentation was obse

72 ondensation, as observed with the use of 4,6-diamidino-2-phenylindole-fluorescent staining, and by de

73 It involves segmenting the 4',6-diamidino-2-phenylindole-labelled image into cells and d

74 mly; locally high levels accumulated in 4',6-diamidino-2-phenylindole-negative zones containing euchr

75 contrast and fluorescence microscopy of 4',6-diamidino-2-phenylindole-stained log phase cells.

76 going apoptosis verifies that the FD of 4',6-diamidino-2-phenylindole-stained nuclear structures does

77 dot-like signal always colocalized with 4',6-diamidino-2-phenylindole-stained nuclei.

78 of polyPs in the acidocalcisomes using 4',6-diamidino-2-phenylindole.

79 embryos were dispersed and treated with 4',6-diamidino-2-phenylindole.

80 by visualization of nuclei stained with 4,6'-diamidino-2-phenylindole.

81 oncept, we evaluated the selectivity of 4',6-diamidino-2-phenylindone (an AT-specific binder), ethidi

82 4,4''-Diamidino-m-terphenyl (1) and 36 analogues were prepared

83 Retrograde tracer diamidino yellow (DY), applied directly to the pial surf

84 ts in mice combining retrograde transport of diamidino yellow after spinal cord injections and immuno

85 ither Cholera Toxin-fluorescein (CT-FITC) or Diamidino Yellow into TPNs revealed that RPM and TPN mot

86 Injections of either Diamidino Yellow or Fluorogold into substantia nigra par

87 fluorescent retrograde tracers Fast blue and Diamidino yellow were placed into different locations wi

88 retrogradely transported dyes Fast Blue and Diamidino Yellow were placed within areas V4 and MT, or

89 True Blue and Diamidino Yellow were used to study the organization of

90 ish this, fluorescent tracers (fast blue and diamidino yellow) were injected into NTS and RVLM, after

91 When retrograde tracers (fast blue and diamidino yellow) were injected into the L5 spinal nerve

92 Applications of horseradish peroxidase, Diamidino yellow, or fast blue to the pial surface of SI

93 The retrograde tracers, Fast blue and Diamidino yellow, were injected at all septotemporal lev

94 y using the retrograde tracers Fast blue and Diamidino yellow.