ライフサイエンスコーパス: Petri dish

1 ulture systems (CS) (a bioreactor system and petri dishes).

2 yramid structures integrated directly into a Petri dish.

3 imulation such as tapping on the side of the Petri dish.

4 ved at the points where the cell touches the Petri dish.

5 rpendicular to the cuts in the center of the petri dish.

6 to design and manipulate cell function in a Petri dish.

7 agarose gels of various compositions cast in Petri dishes.

8 as collected with paper points and plated in Petri dishes.

9 al to the cultures on commercial polystyrene Petri dishes.

10 macroculture systems such as well plates and Petri dishes.

11 dues formed in the lids of 38 mm polystyrene Petri dishes.

12 dices grown monoxenically on bicompartmental petri dishes.

13 ds in different ratios and placing them in a Petri dish after which they are recorded using a camera

14 t allergen dispersal over 20 minutes using a petri dish and immunochromatographic test.

15 ications of SM imaging techniques beyond the petri dish and opens the possibility to explore the mole

16 Subsequent exposure of these "clean" Petri dishes and foil squares to indoor air in two diffe

17 membrane (CAM) of quail embryos cultured in petri dishes and incubated for an additional 24 or 48 ho

18 XS52 cells, ordinarily adhere to petri dishes and phagocytose latex heads, as has been re

19 near-simultaneous image capture of multiple petri dishes and random-access imaging with sub-millisec

20 ells into liquid chambers formed on standard Petri dishes and their subsequent dispensing into vials

21 In vitro (petri dish) and in vivo (greenhouse) studies were conduc

22 lar bag was dissected free, pinned flat on a petri dish, and incubated in Eagle's minimal essential m

23 chemokines are applied onto the surface of a Petri dish, and then immersed under culture medium in wh

24 ng cocultivation with seedlings in bipartite Petri dishes, and (35)S was assimilated from the bacteri

25 ent stages of pregnancy using a static-based Petri dish assay.

26 Smart Petri dish based on this technology can significantly st

27 Unfortunately, traditional Petri dish-based assays overlook much tumor complexity,

28 ental setup suggested uses opaque masks in a Petri dish bathed in ultraviolet radiation, but is based

29 into one macroscopic fluorescent plaque in a Petri dish by plating it in a host bacterial medium.

30 ies grown on glass slides and in polystyrene petri dishes by using light microscopy and scanning and

31 radiata and V. aconitifolia were enclosed in Petri dishes coated with paint containing various concen

32 aining two compartments (BI Petri dish); two Petri dishes connected with tubing; and a microtiter-bas

33 r Arabidopsis or tobacco plant seedlings): a Petri dish containing two compartments (BI Petri dish);

34 were removed and were replaced with sterile petri dishes containing a droplet of sterile brucella br

35 l), a chlorinated polypropylene-coated glass Petri dish (control) and a series of the tannin-function

36 An empty glass Petri dish (control), a chlorinated polypropylene-coated

37 netic field attraction (deflection angle and Petri-dish displacement methods), heating (infrared ther

38 Germination assays were conducted in Petri dishes, each containing 50 seeds, with four groups

39 deposited fractions onto nutrient agar in a Petri dish for microbial culturing, and we subjected the

40 Such devices might be 'electronic Petri dishes' for the direct stimulation of, and measure

41 les, in a lawn of bacteria on an agar-filled Petri dish; however, this rate-limiting step requires up

42 ree experimental and one control groups (6-8 Petri dishes in each group).

43 patially extended bacterial populations in a Petri dish is presented on the basis of an exact formula

44 ecombinant protein to type I collagen-coated Petri dishes is inhibited by anti-65m in a dose-dependen

45 e substrates including polydimethylsiloxane, Petri dishes, Kapton tapes, thermal release tapes, and m

46 On-chip/on-petri dish nanoscale capacitance calibration standards a

47 in neither binds to type III collagen-coated Petri dishes nor inhibits type III collagen and ADP-indu

48 Heating glass Petri dishes or squares of aluminum foil to about 350-40

49 0 droplets/mm2) sprayed on the bottom of the Petri dish, or by flushing N2 above the heptane, the mic

50 ansferred into standard 96-/384-well plates, Petri dishes, or vials for cloning, PCR, and other singl

51 in-functionalized polypropylene coated glass Petri dishes overlaid with linseed oil were exposed to a

52 t this technology can be used to build smart Petri dish platforms, termed ePetri, for cell culture ex

53 Allergen levels in extracts from Petri dish samples, which had been kept frozen, dropped

54 vel, 0.0, 0.5, 1.0, and 2.0 m, using passive petri dish sampling to collect airborne bacteria.

55 e with the polystyrene floor of one group of Petri dishes serving as the control.

56 e gradients could be easily transferred to a petri dish surface by stamping.

57 The optimized procedure for the BI Petri dish system is described in this protocol and can

58 ide FOV time-lapse fluorescence self-imaging Petri dish system, termed the Talbot Fluorescence ePetri

59 onchiseptica, by direct contact with an agar petri dish, than rabbits with bacteria alone.

60 By fixing multiple gel beads in a Petri dish, the cores become linked to one another by th

61 e are printed in seconds on plastic or glass Petri dishes; then, interfacial forces pin liquids to su

62 natural compound functionalized PVC covered Petri dish to undergo autoxidation under white light.

63 ditions (wet, tissue culture media in, e.g., Petri dishes) to more realistic conditions (dried, simul

64 Conventionally, they are performed in Petri dishes, tubes, or well plates, using milliliters o

65 a Petri dish containing two compartments (BI Petri dish); two Petri dishes connected with tubing; and

66 dothelial cells (bPAECs) to the surface of a Petri dish were investigated.

67 sected alimentary tracts, and excreta on the petri dishes were cultured for H. pylori, whose identity

68 Forty petri dishes were divided into 4 equal groups.

69 iological and histological analysis, and the petri dishes were replaced with fresh sterile plates wit

70 Petri dishes were used to collect airborne dust samples

71 for cell immobilization included coating the Petri dish with 100 microg/mL fibronectin, a seeding cel

72 living bacterial colonies directly from the Petri dish with absolutely no sample preparation needed.

73 atory diagnosis could be made using only one petri dish with sliced agar, thereby saving time and med

74 or none), the methods of microbial sampling (petri dishes with solid media, filter paper discs, air h

75 ion of human neutrophils adherent to plastic petri dishes with the purified chemotactic factors C5a a

76 g of live microbial colonies directly from a Petri dish without any sample preparation.

77 in order to recapitulate reprogramming in a Petri dish without the use of oocytes.

78 We grew wheat seedlings in sealed petri dishes without obstacle and in custom 3D-printed r

79 bial colonies grown on soft nutrient agar in Petri-dishes without any sample pretreatment.

80 ctly from living bacterial colonies grown in Petri dishes, without any sample pretreatment.