ライフサイエンスコーパス: 4',6-diamidino-2-phenylindole

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

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

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

4 ization of polyP in the dense granules using 4',6-diamidino-2-phenylindole and by its release togethe

5 taining with anti-alpha-tubulin antibody and 4',6-diamidino-2-phenylindole and flow cytometric analys

6 ibe activation of the channel by diminazene, 4',6-diamidino-2-phenylindole, and pentamidine, examine

7 rns after combined propidium iodide (PI) and 4', 6-diamidino-2-phenylindole (DAPI) staining.

8 pected for intracapsid steric restriction of 4',6-diamidino-2-phenylindole (DAPI) binding to packaged

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

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

11 ing magnetic resonance imaging, mCherry with 4',6-diamidino-2-phenylindole (DAPI) staining and green

12 tending toxin (Cdt), connective tissue (CT), 4',6-diamidino-2-phenylindole (DAPI), human gingival epi

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

14 tron microscope after labeling in vitro with 4',6-diamidino-2-phenylindole (DAPI), intracellular inje

15 4',6-diamidino-2-phenylindole (DAPI), netropsin, and pen

16 nuclei frequently do not stain equally with 4',6-diamidino-2-phenylindole (DAPI), suggesting that by

17 ex affinity exhibited by 5PTB, netropsin and 4',6-diamidino-2-phenylindole (DAPI), two AT-specific mi

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

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

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

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

22 en bond with the minor groove binding ligand 4',6-diamidino-2-phenylindole (DAPI).

23 de macrophages were stained with the DNA dye 4',6-diamidino-2-phenylindole (DAPI).

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

25 t methods: staining intact chloroplasts with 4',6-diamidino-2-phenylindole (DAPI); staining at the si

26 ely charged dyes, propidium iodide (PrI) and 4'-6-diamidino-2-phenylindole (DAPI).

27 le chromosome probes, single-copy genes, and 4'-6-diamidino-2-phenylindole (DAPI-) and G-banded chrom

28 ick-end labeling (TUNEL) in conjunction with 4'6'-diamidino-2-phenylindole (DAPI) staining and by flu

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

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

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

32 inor groove binding compounds, netropsin and 4,6-diamidino-2-phenylindole (DAPI), and a DNA hairpin h

33 of cell extracts, and staining of cells with 4,6-diamidino-2-phenylindole (DAPI), and the polyP-bindi

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

35 s, the peptide gramicidin, and a DNA-ligand (4',6-diamidino-2-phenylindole, DAPI) system in this work

36 Cytochemical staining of cellular DNA with 4,6-diamidino-2-phenylindole demonstrated TNF-alpha-indu

37 ensitive fluorescent reagents SYPRO Ruby and 4',6-diamidino-2-phenylindole dihydrochloride (DAPI), to

38 Apoptosis was evaluated by 4',6-diamidino-2-phenylindole dihydrochloride and termin

39 /PMS kit and of dead (apoptotic) cells using 4',6-diamidino-2-phenylindole dihydrochloride nuclear st

40 uorescent dye molecules per CPMV using DAPI (4',6-diamidino-2-phenylindole dihydrochloride), propidiu

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

42 NA was stained with propidium iodide (PI) or 4',6-diamidino-2-phenylindole, dihydrochloride (DAPI).

43 Furthermore, microtubule immunostaining and 4,6-diamidino-2-phenylindole DNA staining demonstrated t

44 in condensation, as observed with the use of 4,6-diamidino-2-phenylindole-fluorescent staining, and b

45 These cells were later stained with 4', 6-diamidino-2-phenylindole for simultaneous DNA anal

46 cell level using double immunostaining plus 4,6-diamidino-2-phenylindole (for nuclei) counterstainin

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

48 DAPI (4,6-diamidino-2-phenylindole) inhibited the assembly of

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

50 unctate nuclear localization correlated with 4,6-diamidino-2-phenylindole light regions and is exclud

51 niformly; locally high levels accumulated in 4',6-diamidino-2-phenylindole-negative zones containing

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

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

54 of fixed permeabilized red blood cells with 4',6'-diamidino-2-phenylindole or YOYO-1, a sensitive nu

55 ite-specific probes, in addition to inverted 4,6-diamidino-2-phenylindole or conventional G-banding a

56 fluorescent foci that colocalize with DAPI (4',6'-diamidino-2-phenylindole)-positive material and fo

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

58 undergoing apoptosis verifies that the FD of 4',6-diamidino-2-phenylindole-stained nuclear structures

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

60 distribution of the actin cytoskeleton, DNA (4', 6-diamidino-2-phenylindole staining), and calcofluor

61 e-contrast microscopy, and in selected cases 4',6'-diamidino-2-phenylindole staining and DNA fragment

62 4',6'-diamidino-2-phenylindole staining demonstrated tha

63 poptotic, as assessed by Annexin V staining, 4',6'-diamidino-2-phenylindole staining, and DNA fragmen

64 We also used 4',6-diamidino-2-phenylindole staining of isolated plast

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

66 ase-mediated dUTP nick-end labeling (TUNEL), 4',6-diamidino-2-phenylindole staining, and immunohistoc

67 ristic apoptotic changes, as demonstrated by 4',6-diamidino-2-phenylindole staining, lack of either D

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

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

70 ing a combination of chromosome painting and 4',6-diamidino-2-phenylindole staining.

71 titanium surfaces were measured according to 4'-6-diamidino-2-phenylindole staining.

72 romatin fragmentation by acridine orange and 4'6-diamidino-2-phenylindole staining, and (3) agarose g

73 nd changes in nuclear morphology detected by 4,6-diamidino-2-phenylindole staining, DNA fragmentation

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

75 Also, DAPI (4',6'-diamidino-2-phenylindole) staining revealed that c

76 mal fragmentation of cellular DNA, and DAPI (4',6-diamidino-2-phenylindole) staining revealed condens

77 deoxyuridine (BrdU) pulse-labeling and DAPI (4',6-diamidino-2-phenylindole) staining, which precisely

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