ライフサイエンスコーパス: serum-free media

1 n synthase kinase-3 (GSK3) inhibitor, and in serum-free media.

2 ined, even when these cells were cultured in serum-free media.

3 fection using standard cell culture media or serum-free media.

4 WNT signaling, cell growth, and survival in serum-free media.

5 ter monolayer expansion, and after 1 week in serum-free media.

6 hneider insect (S2) cells, and purified from serum-free media.

7 and then TGF-beta2 was added for 24 hours in serum-free media.

8 and at 5 DPS media were replaced with fresh serum-free media.

9 olated rabbit keratocytes plated in defined, serum-free media.

10 ic phenotype and appearance when cultured in serum-free media.

11 tes also cleave IgG in both growth media and serum-free media.

12 roliferation and motility when maintained in serum-free media.

13 st model, cells were grown in low density on serum-free media.

14 ptosis and that apoptosis was potentiated in serum-free media.

15 and 100 micrograms/ml) for up to 48 hours in serum-free media.

16 m is 22 days) were incubated in hormone- and serum-free media.

17 ry explants were generated and maintained in serum-free media.

18 al cells results in sustained cell growth in serum-free media, a predisposition to develop hyperplasi

19 ectin (VN), or collagen (CL) in supplemented serum-free media alone or with TGF-beta1 or fibroblast g

20 proteoglycans synthesized by keratocytes in serum-free media also more closely resembled that of ker

21 d (G12V)Ha-ras or (Q61K)N-ras proliferate in serum-free media and have constitutive MAPK activity.

22 atal neurons grown in low density culture on serum-free media and in the absence of glia die within 3

23 -alpha) in fetal bovine serum-containing and serum-free media and were analyzed by Wright's stain for

24 sham-operated rats, cultured on Matrigel in serum-free media, and briefly exposed to rat cytomegalov

25 roliferation induced by nonconducting EAG in serum-free media, and EAG increased p38 MAP kinase activ

26 sal-like phenotype in vitro when cultured in serum-free media, and undergoes phenotypic changes consi

27 Furthermore, cultured RGC maintained in serum-free media are also C1q and C3 immunoreactive, dem

28 well tissue culture plates and maintained in serum-free media at 37 degrees C.

29 ly isolated chondrocytes died when plated in serum-free media at low density on poly-L-lysine, but sh

30 f complement on CD19 loss was examined using serum-free media, C3- and C5-deficient sera, and a C5-bl

31 Also, serum-free media conditioned by transiently compressed g

32 CSp-EMVs were isolated from serum-free media conditioned for 3 days by cardiospheres

33 ult (12 weeks) rat ganglia and maintained in serum-free media containing glucose (10-100 mM) in the p

34 her concentrations of PLL (1.5 microg/mL) in serum-free media during initial FE-PLL complex formation

35 l as acutely isolated astrocytes cultured in serum-free media, failed to respond to 5-HT by changes i

36 cubated in either control, acid, or alkaline serum-free media for 12 h.

37 Confluent cells were exposed to serum-free media for 24 h, then incubated in either cont

38 SC were cultured as free-floating pellets in serum-free media for 3 weeks.

39 e agonists/antagonists to their receptors in serum-free media for 5-7 days.

40 uccessful use of an ITS+ Premix-supplemented serum-free media for prolonged islet culture and its com

41 ddition of TGF-beta1 to endothelial cells in serum-free media further potentiated the induction of ap

42 TRA-1-60(-)/SSEA4(-)/SOX1(+) cells grown in serum-free media give rise to multipotent NSCs with an e

43 ultured in gas-permeable bags containing 1-L serum-free media, granulocyte colony-stimulating factor,

44 rapidly increased after exposure of cells to serum-free media, heat shock, or staurosporine.

45 n as VEGFA) and dickkopf homolog 1 (DKK1) in serum-free media, human embryonic-stem-cell-derived embr

46 an pancreatic cells were proliferated with a serum-free media in monolayer cultures through multiple

47 ed marker shows spheroid colony formation in serum-free media in vitro, as well as tumorigenic abilit

48 neration lentiviral vector in FreeStyle 293 (serum-free media) in suspension.

49 NA levels in neuroblastoma cells cultured in serum-free media increased after 8 to 16 hours in BDNF.

50 The serum-free media-induced decrease in permeability was co

51 incubation of mouse embryonic fibroblasts in serum-free media induces caspase-3 activation, an effect

52 TGF-beta1 to vascular smooth muscle cells in serum-free media inhibited apoptosis.

53 Culturing human islets in Memphis serum-free media (M-SFM) is associated with excellent po

54 In defined, serum-free media, NHBEs undergo mucosecretory differenti

55 Exposing cells to serum-free media on their basolateral side significantly

56 However, when cells were grown with either serum-free media or at high densities, CDK2 levels decli

57 and express five-fold fewer IGF-IRs, die in serum-free media or following exposure to metabolic stre

58 In serum-free media, p50E4F accelerated E1A-induced apoptos

59 ated dishes and cultured for up to 7 days in serum-free media, platelet derived growth factor BB (PDG

60 However, culture in serum-free media, presence of nerve growth factor, or ad

61 o the apoptotic effect of PI3K inhibition in serum-free media, reflecting the heterogeneous nature of

62 ures of hepatocytes and endothelial cells in serum-free media seeded under 95% oxygen maintain functi

63 ent of cells with tyrphostin AG879 prevented serum-free media (SFM) induction of cell proliferation.

64 were cultured in parallel in (A) CMRL + ITS (serum-free media; SFM) or (B) CMRL +10% fetal bovine ser

65 Growth in either serum-containing or serum-free media supplemented with GM-CSF and IL-4 yield

66 Here, we define in serum-free media the minimal factor requirement controll

67 Pellet cultures of hCSSC in serum-free media upregulated the expression of keratocyt

68 This increased proportion of KS synthesis in serum-free media was caused by a moderate increase in KS

69 media and forms neurospheres in supplemented serum-free media was developed from retinal tumors isola

70 cells, NGF's ability to promote survival in serum-free media was reduced.

71 NTM5 and GTM3) human TM cells conditioned in serum-free media were incubated in the absence or presen

72 an as keratan sulfate (KS), whereas cells in serum-free media were quiescent, appeared dendritic, and

73 aT-AR) displayed autonomous proliferation in serum-free media when compared with controls (HaCaT-NIE)

74 ts before SCT, which were cultured 4 days in serum-free media with hematopoietic growth factors.

75 growth factor and hematopoietic cytokines in serum-free media, yielded a precursor population enriche