ライフサイエンスコーパス: culture plate

1 n the basolateral compartment (BC) of a cell culture plate.

2 r extraction of proteins from cells within a culture plate.

3 bservation of bacteria colonies growing on a culture plate.

4 s constructed at the bottom of a medusa cell culture plate.

5 ls prepared in advance in a multiwell tissue culture plate.

6 re seeded in each of four chambers of a cell culture plate.

7 ion of these cells detaching from the tissue culture plate.

8 nt cells round up and detach from the tissue culture plate.

9 cell proliferation between brands of tissue culture plates.

10 tracted directly from samples or from washed culture plates.

11 oparticles is formed via dip-coating of cell culture plates.

12 selective adhesion to collagen-coated tissue culture plates.

13 seeded and grown in fourteen 96-well tissue culture plates.

14 violet-based assay involving 24-well tissue culture plates.

15 method of precoating retroviral vectors onto culture plates.

16 al cells by casting agarose strips on tissue culture plates.

17 owth of isolated colonies adhering to tissue culture plates.

18 -, or fibronectin-coated or noncoated tissue culture plates.

19 anted tissue, and passaged to 12-well tissue culture plates.

20 anted tissues and passaged to 12-well tissue culture plates.

21 r domain of C-cadherin immobilized on tissue culture plates.

22 ayers also were treated in EMD coated tissue culture plates.

23 cell monolayers across the length of tissue culture plates.

24 ated with EMD in medium versus EMD coated on culture plates.

25 t induction periods and using various tissue culture plates.

26 e removed from SC and cells seeded onto 3-cm culture plates.

27 vated concomitant with cell adherence to the culture plates.

28 membrane inserts and placed in 6-well tissue culture plates.

29 itous in our environment and may contaminate culture plates.

30 iminated the nonspecific binding to the cell culture plate and decreased the overall background of th

31 monolayers across the diameter of the tissue-culture plate and determining PDL cell migration into th

32 rons co-cultured with SCs dispersed over the culture plate and had extensive neuritic outgrowth, whil

33 was achieved by detaching the cells from the culture plate and reseeding them at a 1:4 ratio.

34 cell activity compared to the reference cell culture plate and the highest power output was ITO.

35 ives organoids transferred from their native culture plates and anchors them, respectively.

36 appearance and subsequently detach from the culture plates and die or they may remain intact in a hi

37 t 2.5 x 10(4) cells/well into 48 well tissue culture plates and maintained in serum-free media at 37

38 g inhibited the attachment of tumor cells to culture plates and the adherence and extravasation in th

39 medium for 1 day to allow attachment to the culture plates and then cultured in serum-free DMEM, wit

40 multiple sample types and formats (biofluid, culture plate, and pellet) and show that in all cases, i

41 , infected MDCK-London cells in 96-well cell-culture plates are processed with minimal steps such tha

42 their ability to differentiate into SMCs in culture plates as well as in a bioreactor system.

43 Fewer cells attached to the culture plates at 48 hr in the ischemia group.

44 Stem cells were seeded into 6-well culture plates at a density of 350,000 cells per well.

45 and promotes chondrogenic differentiation in cultures plated at subthreshold cell densities that are

46 were synthesized and used to pre-coat tissue culture plates before lung derived ASM cells and fibrobl

47 cells was increased by incubation on tissue culture plates coated with these matrix proteins; this e

48 In cells adhering to culture plates coated with vascular cell adhesion molecu

49 RAPD fingerprints obtained from primary culture plate colonies allows for rapid, highly accurate

50 T3 cells that express it form foci in tissue culture plates, colonies in soft agar, and tumors in nud

51 showing satellitism were passaged onto fresh culture plates cross-streaked with potential helper stra

52 d reached confluence as monolayers on tissue culture plates (EC-TCPS).

53 b or human IgG, when immobilized onto tissue culture plates, facilitated eosinophil cell death even i

54 at larval fish bioassays conducted in tissue culture plates fitted with polycarbonate membrane insert

55 udies utilizing flow cytometry or multi-well culture plate fluorometry are often limited by a deficit

56 f 64 mM NaIO4 for 20 min in a 96-well tissue culture plate followed by a measurement of absorbance at

57 anged into a gel-based array directly from a culture plate for downstream processing and analysis.

58 endothelial cells (HUVECs) in 24-well tissue-culture plates for 12 hours.

59 endon explants, and were incubated in 6-well culture plates for 2 periods of 48 hours each, with cipr

60 hepatocytes were incubated in standard cell culture plates for 24 hrs before the addition of nonpare

61 re removed and allowed to dry then placed in culture plates for each time point.

62 inherent in the ordered array of the 24-well culture plate format, resulting in a semi-automated smal

63 of cell culture media from H460 cancer cell culture plates from day 0 to day 5 can easily be determi

64 The agar culture plate has played a crucial role in bacteriology

65 rin-dependent binding to gal-3-coated tissue culture plates; however, binding is attenuated upon forc

66 adhesion of mononuclear phagocytic cells to culture plates in association with other nucleated and n

67 PBMCs were added to 12-well culture plates in four groups of media: a) control; b) c

68 lobal interpretation of diagnostic bacterial culture plates, including presumptive pathogen identific

69 CD9 mAb (clone ALB6) immobilized onto tissue culture plates induced eosinophil degranulation.

70 As HOS cells are adherent to culture plates, infected T cells in suspension can be ea

71 F antibody to cells grown in Matrigel-coated culture plates inhibited 12(R)-HETrE-induced capillary t

72 lishing the presence or absence of growth on culture plates inoculated with a series of dilutions and

73 delivery of the mixed solutions into tissue culture plates is actuated by a novel mechanism based on

74 Culture plating is worldwide accepted as the gold standa

75 enthamiana) and demonstrated, when coated on culture plates, its osteogenic induction capacity of hum

76 nt using a 10-mul inoculum with results from cultures plated manually with a 1-mul loop for comparabl

77 egrin-binding fragment of Invasin, coated on culture plates, mediated gut epithelial cell adhesion.

78 The SIA-SPR method together with the culturing (plating) method was able to detect C. jejuni

79 outside of the cell membrane and to the cell culture plate occurred for some compounds.

80 ical environment are largely limited to cell culture plated on a two-dimensional substrate.

81 LCA) to determine a representative subset of culture plates on which to conduct culture-enriched meta

82 The addition of IGFBP-5 to cultures plated on laminin and type IV collagen signific

83 ency firing was recorded in primary neuronal cultures plated on multielectrode arrays; (2) thalamocor

84 Using CNS mixed myelinating rat cultures plated on to a monolayer of astrocytes, we demo

85 en significant growth and no growth of urine cultures plated onto standard blood and MacConkey agars.

86 or the ability of the cells to anchor to the culture plate or extracellular matrix and does not block

87 contralateral flattened surfaces facing the culture plate or the medium.

88 is includes plating cells on six-well tissue culture plates or imaging dishes, treatment with CuFL, s

89 pressing the p.D22G mutant detached from the culture plate over time, became terminal deoxynucleotidy

90 monolayers detached from the surface of the culture plate postinfection, in contrast to the 3-D aggr

91 The Elek culture plate precipitin test is routinely used for the

92 f cyanide with cell culture media in 96-well culture plates reduced cyanide concentrations rapidly (8

93 -DOTAP complex; a DNA dose of 4 microg/35 mm culture plate seeded with 2.5x10(5) rat hepatocytes.

94 ere placed into the wells of a 6-well tissue culture plate, stacked onto a reader unit and could thus

95 le of subgingival plaque was inoculated onto culture plates supplemented with siderophores (pyoverdin

96 adjacent cells, eventually sloughing off the culture plate surface, with most cell deaths occurring b

97 the culture conditions revealed that tissue culture plates (TCPs) coated with a tissue-specific extr

98 ovine serum, the configuration of the tissue culture plate, the temperature at which the bacteria are

99 y, and the nonspecific binding with the cell culture plates, the extracellular matrices, and the cell

100 lls that grew loosely associated with tissue culture plates; this correlated with reduced levels of b

101 rticles by exposing cells at the bottom of a culture plate to a suspension of nanoparticles, and it i

102 ent MS analysis in less than 2 h from a cell culture plate to final MS data.

103 erated, incorporated BrdU, migrated onto the culture plate to form monolayers, and phagocytized ROS.

104 or 21 days whereas cells cultured in regular culture plates under identical conditions de-differentia

105 s and immobilized on the surface of a tissue culture plate was able to stimulate hybridomas derived f

106 Using Transwell culture plates, we further demonstrated that physical co

107 ingly, we created a macrofluidic model using culture plate wells connected with type I collagen-coate

108 feration could be demonstrated by precoating culture plate wells with EMD.

109 When the culture plates were coated with collagen, < 100 microgra

110 f the cells rounded up and detached from the culture plate, whereas nM cholesterol had no such effect

111 in cells cultured upon specialist electrode culture plates which allow for continuous, non-invasive

112 of 20 species could be extracted from a 24-h culture plate, while the remainder required 48-72 h.

113 of their adherence by rocking or by covering culture plates with polyhydroxyethylmethacrylate resulte

114 d and automatically deposited into a 96-well culture plate within 1 min.

115 int similar to that of a common 24-well cell culture plate within which each well is electrified via

116 to analyze microbial cultures directly from culture plates without any prior preparation.

117 lly manipulate live microtissues into/out of culture plates without using complicated accessories suc

118 yed experimental apparatuses: 24-well tissue culture plates (WP), muscle myograph baths (MB), and the