ライフサイエンスコーパス: were incubated for

1 Rat pancreatic acini were incubated for 1-4 hours with FAEEs or acetaldehyde.

2 The bottles were incubated for 5 days; 32 control and 104 test bottles we

3 Confluent cultures of rat CECs were incubated for 24 hours in the presence of p27(kip1) anti

4 Cells were incubated for 24, 48, and 72 hours.

5 To assay changes in the actin cytoskeleton, TM-1 cells were incubated for 24 hours with or without the HepII domain,

6 FG human pancreatic adenocarcinoma cells were incubated for various time periods in media at a physiol

7 After Chase I, cells were incubated for another hour (C2) with/without brefeldin A

8 If cells were incubated for 24 hours with 5-FC followed by a 24-hour G

9 ated for a longer period of time to allow maturation, cells were incubated for 8 days in LD followed by 2 days in DD.

10 TM cells were incubated for 1 hour at 4 degrees C with biotinylated al

11 ations, the class 2 phenotype could be corrected when cells were incubated for 24 hours at reduced temperature (27 degree

12 When cells were incubated for sufficient time to allow for endocytosis (

13 Whole human corneas were incubated for 2 hours in a solution of recombinant E1(-)

14 After transfection, corneas were incubated for various periods in 0.1% FBS (a concentrati

15 To assess dye uptake, cultures were incubated for 5 minutes with 0.1% rose bengal and photog

16 murine splenocytes and from blood samples of healthy donors were incubated for 8 days under Th2-like conditions with aque

17 e samples (undiluted) spiked with E. coli or N. gonorrhoeae were incubated for 5 min with 1% Tween 80.

18 Transformed human TM cells (GTM3) were incubated for 24 hours in the presence of activated lova

19 d culture samples from patients with bloodstream infections were incubated for 1 h with the "smart" activatable P2&3TT pr

20 Phenotypically different cell lines were incubated for 1, 3, 6, and 10 days in 0.2% fetal bovine

21 Unfractionated BMDSC from diabetic Lepr mice were incubated for 20 hours with SDF-1alpha (100 ng/mL) or bo

22 ary cultures of neurons and glial cells from Npc1(-/-) mice were incubated for 24 h with 0.1 to 10 mm CD after which surv

23 LLC-PK1 monolayers were incubated for 1, 3, 6, or 12 h with 0% or 5% O2 or 300 m

24 For ex vivo studies, SVG segments from 24 patients were incubated for 6 hours with atorvastatin 0, 5, or 50 mumo

25 Corneal pieces were incubated for 24, 36, 48, 60, 72, 84, and 96 hours in me

26 The plates were incubated for 7 days at room temperature, and colonies w

27 Isolated PMNs were incubated for 6 hours with or without CH 11, a CD95 agon

28 Mice infected with H. polygyrus were incubated for 2 weeks, followed by P. aeruginosa intrana

29 Hepatocytes isolated from adult male Sprague-Dawley rats were incubated for 4 hours in buffer containing the hydrophob

30 Pituitary segments from male rats were incubated for 5, 10 or 20 min in Earle's balanced salt s

31 extensor digitorum longus muscles isolated from normal rats were incubated for 1 hr in the Krebs-Henseleit buffer media c

32 extensor digitorum longus muscles isolated from normal rats were incubated for 1 hr in the Krebs-Henseleit buffer media c

33 Human CBSM cells isolated from donor corneoscleral rims were incubated for 24 hours with control (0.015% ethanol in D

34 Nearly 90% of the ovules aborted when roots were incubated for 12 h in a hydroponic medium supplemented w

35 Samples were incubated for 24 hours with control solution or methylgl

36 Samples were incubated for 24 hours with control solution or methylgl

37 oaerosol impactors with nutrient and soy media, and samples were incubated for 48 hours at 37 C with 5% CO(2).

38 All sputum samples were incubated for detection of mycobacterial growth and thos

39 These samples were incubated for various times at different temperatures (4

40 After seeding at 15 x 10(6) cells/cm2, scaffolds were incubated for 10 days in a roller bottle with or without

41 After seeding at 2 x 10(6) cells/cm2, scaffolds were incubated for 5 days in a roller bottle, with or without

42 In the ex vivo model, posterior segments were incubated for up to 120 minutes in peptide solution.

43 broblasts attached to collagen-glycosaminoglycan substrates were incubated for 5 wk in media containing 0.0 mM or 0.1 mM

44 ls isolated from lung samples incidental to patient surgery were incubated for 24 h (overnight) in medium (control) or 1

45 Preparations that were incubated for longer than 24 h contained significantly m

46 h muscle strips by reversible permeabilization, and tissues were incubated for 2 days to allow for protein expression.

47 oduced into tracheal smooth muscle tissues, and the tissues were incubated for 2 days to allow for protein expression.

48 The vials were incubated for 72 h, and aliquots were removed for HPLC a

49 For the in vitro wound assay, triplicate wells were incubated for 1, 3, 5, and 7 days using 0.1% fetal bovin

50 te and a synthetic Opalinus Clay pore water solution, which were incubated for one year at 30 and 60 degrees C.