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

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

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

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

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

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

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

13 4',6-diamidino-2-phenylindole (DAPI), netropsin, and pen

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

57 4',6'-diamidino-2-phenylindole staining demonstrated tha

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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