ライフサイエンスコーパス: supernatant fluid

1 of a large quantity of the Gag p27 into the supernatant fluid.

2 le amounts of the LspA1 protein into culture supernatant fluid.

3 that can be detected in concentrated culture supernatant fluid.

4 d in the release of virus particles into the supernatant fluid.

5 ibody was used to localize the enzyme in the supernatant fluid.

6 ount of NADase and SLO activities in culture supernatant fluids.

7 bstantially more H77-S RNA was secreted into supernatant fluids.

8 hanisms for regulating RTX toxin activity in supernatant fluids.

9 iation with the appearance of sVCAM-1 in the supernatant fluids.

10 surable IFN-gamma expression was detected in supernatant fluids.

11 or 6 h, and IL-1 was measured in the culture supernatant fluids.

12 ith RSV and determined nitrite levels in the supernatant fluids.

13 ol of product formed was readily detected in supernatant fluids.

14 the numbers of tachyzoites released into the supernatant fluids.

15 ion of LspA proteins from H. ducreyi culture supernatant fluid abolished this inhibitory effect, indi

16 ite presence of MGCs and infectious virus in supernatant fluids after apical infection, infected cell

17 LspA1 protein that was detectable in culture supernatant fluid and no LspA2 protein.

18 by measuring alpha-toxin activity in culture supernatant fluids and by Northern analysis of the alpha

19 in, RTX (repeats-in-toxin) toxin, to culture supernatant fluids and that this toxin is responsible fo

20 onuclear cells after harvesting of cell-free supernatant fluids at peak antigen production (days 4-7)

21 vitro, human CCA cells were treated with MC supernatant fluids before evaluating angiogenesis and EM

22 gene cluster and can be detected in culture supernatant fluid by its ability to kill HeLa cells.

23 analysis of eHAV purified from cell-culture supernatant fluids by isopycnic ultracentrifugation.

24 ese cells, and because megakaryocyte-derived supernatant fluid can reproduce the EndMT switch in vitr

25 specific activities of AA released into the supernatant fluid closely mimicked that of PtdEtn.

26 We observed that supernatant fluids collected from macrophages incubated

27 in cell-free concentrated H. ducreyi culture supernatant fluid could also be tyrosine phosphorylated

28 Culture supernatant fluid from a recombinant Escherichia coli st

29 Supernatant fluid from cultured explants of RCC, but not

30 M. catarrhalis cells or in the spent culture supernatant fluid from M. catarrhalis.

31 creased when UV-inactivated MV or virus-free supernatant fluid from MV-infected PBMCs was used.

32 Culture supernatant fluid from this H. ducreyi cdtC mutant did n

33 Supernatant fluids from C. albicans markedly induced the

34 Concentrated culture supernatant fluids from H. ducreyi lspB and lspA1 lspB m

35 TX-associated activity is detectable only in supernatant fluids from log phase cultures.

36 IL-1beta-rich supernatant fluids from oral streptococci-stimulated or

37 We used supernatant fluids from peripheral blood mononuclear mon

38 Supernatant fluids from the cultures were analyzed for l

39 Supernatant fluids from the PBMC cultures were harvested

40 recombinant IL-1beta was comparable with the supernatant fluid in activity.

41 LspA1 nor LspA2 could be detected in culture supernatant fluid in the absence of FCS.

42 -ERK44/42 MAPK levels induced by C. albicans supernatant fluids in the IFN-gamma-plus-LPS-driven mono

43 MC supernatant fluids increased CCA histidine decarboxylase

44 nce of RTX toxin in stationary-phase culture supernatant fluids is also due to a lack of toxin secret

45 l inoculation with virions from concentrated supernatant fluid, JSRV-associated OPC lesions were foun

46 The present data show that, unlike supernatant fluids obtained from S. cerevisiae, the C. a

47 mmonium sulfate at 100% saturation by use of supernatant fluid of BCSP70 that had been precipitated w

48 type protein (CGCryV) has been isolated from supernatant fluids of Bacillus thuringiensis AB88 cultur

49 rified by immunoaffinity chromatography from supernatant fluids of encystment cultures.

50 ked immunosorbent assay (ELISA) performed on supernatant fluids of LPS challenged MDM showed ImI-medi

51 eta-glucosidase that is added exogenously to supernatant fluids of the null tissue extracts.

52 SPE B was detected in broth culture supernatant fluid only during the stationary phase of gr

53 . gingivalis CPS and assessed the ability of supernatant fluids produced by challenged macrophages to

54 h nitrite concentrations in the LA-4 culture supernatant fluids (r2 = 0.848 and 0.956).

55 obtained from S. cerevisiae, the C. albicans supernatant fluids significantly suppressed IL-12 produc

56 nditions, in concentrated H. ducreyi culture supernatant fluids that lacked detectable outer membrane

57 red necessary for H. ducreyi-derived culture supernatant fluid to exhibit cytotoxicity for HeLa cells

58 pressed in order for E. coli-derived culture supernatant fluids to demonstrate cytotoxicity for HeLa

59 otein that was readily detectable in culture supernatant fluid together with a barely detectable amou

60 dissected cytology slides and from discarded supernatant fluid was analyzed in 26 patients with atypi

61 ing that the IL-12p40 homodimer found in the supernatant fluid was biologically active.

62 2:1) to stimulate IL-12, concentrated fungal supernatant fluids were added and incubated for an addit

63 Supernatant fluids were obtained from cultured C. albica

64 ht patients showed no evidence of fat in the supernatant fluid with either CT (n = 7) or CT and MR im