ライフサイエンスコーパス: Percoll

1 of 35% Metrizamide, 17% Metrizamide, and 6% Percoll.

2 t prevents interference from Metrizamide and Percoll and determines total protein content, and a succ

3 res of monkey kidney E6 cells, purified with Percoll, and exposed to homologous and heterologous rabb

4 L.) were purified from unpollinated ears via Percoll centrifugation.

5 coupled with a modified technique involving Percoll centrifugation.

6 Percoll density centrifugation is simple, can be done on

7 sduction protocol that uses simple and rapid Percoll density centrifugation to enrich RV-susceptible

8 ultures could be dissociated and enriched by Percoll density centrifugation to give a population cont

9 feeding ticks by velocity centrifugation and Percoll density gradient centrifugation.

10 cosediments with lysosomal enzyme markers by Percoll density gradient centrifugation.

11 rat brain mitochondria were obtained using a Percoll density gradient method.

12 crophages by differential centrifugation and Percoll density gradient subcellular fractionation.

13 14CO2 production from L-[14C]glutamine in Percoll density gradient-purified E. risticii was not in

14 llet upon centrifugation and from entering a Percoll density gradient.

15 d subcellular compartments were separated on Percoll density gradients analyzed with T cells.

16 d from guinea pig liver by centrifugation on Percoll density gradients and compared to Percoll-purifi

17 Using Percoll density gradients, PMN were isolated (concentrat

18 nriched nuclear fractions are obtained using Percoll density gradients.

19 tribution of mutant forms of the receptor by Percoll density gradients.

20 rs, smokers, and patients with COPD by using Percoll density gradients.

21 (NK) cells (96% CD16(+)/CD3(-)) isolated by Percoll discontinuous density gradient of peripheral blo

22 Mitochondria were isolated using Percoll discontinuous gradients in combination with high

23 of sustained hypoxia of primary cultures of Percoll-enriched neonatal rat cardiac myocytes was used

24 t density solutions, CsCl for microbeads and Percoll for cells.

25 tein, which was also detectable in the dense Percoll fraction.

26 Ex vivo, Percoll-fractionated B cells expressing a kappa transgen

27 phils were separated from whole blood over a Percoll gradient and then activated via the Fcgamma rece

28 were purified by a combination of isopycnic Percoll gradient centrifugation and continuous sucrose g

29 spores from bacterial contaminants involved Percoll gradient centrifugation followed by additional s

30 tochondria were purified by differential and Percoll gradient centrifugation, and mtODE was extracted

31 Peripheral blood basophils were separated by Percoll gradient centrifugation, cultured overnight, and

32 oroplasts by differential centrifugation and Percoll gradient centrifugation.

33 lization of radioactivity were determined by Percoll gradient centrifugation.

34 ched fraction of plasma membrane prepared by Percoll gradient centrifugation.

35 fractions of resting neutrophils isolated by Percoll gradient fractionation and free flow electrophor

36 Percoll gradient fractionation demonstrated decreases in

37 conjugates using cellular-radioimmunoassays, Percoll gradient fractionation of cell organelles, SDS-P

38 ated differential centrifugation followed by Percoll gradient fractionation, ultrapure, never frozen

39 s using sequential discontinuous sucrose and Percoll gradient fractionation.

40 from early to late endosomes as measured by Percoll gradient fractionation.

41 ain mitochondria isolated by a discontinuous Percoll gradient method was calculated to be -171 mV bas

42 by passage through a glass bead column or a Percoll gradient or by dialysis.

43 ocal microscopy of Snn-transfected cells and Percoll gradient purification of mitochondria showed Snn

44 With Percoll gradient separation, two predominant culture sub

45 system, together with anti-trout Ig Abs and Percoll gradient separation, we analyzed B cells from tr

46 ver mitochondria isolated by a discontinuous Percoll gradient show an oxidized redox environment, whi

47 ecal debris, only oocysts recovered from the Percoll gradient were free of bacteria.

48 isolated from protoplasts and purified on a Percoll gradient were highly import-competent, with litt

49 zymogen granules were further purified on a Percoll gradient, InsP3 receptors were undetectable, and

50 By a Percoll gradient, we were able to separate these two typ

51 Percoll gradient-purified brain synaptic and non-synapti

52 lar fractionation of endocytic vesicles on a Percoll gradient.

53 were separated by density in a discontinuous Percoll gradient.

54 ival tissue were applied to a single-density Percoll gradient.

55 medium and further purified using a two-step Percoll gradient.

56 onal role for the mitoKATP in brain, we used Percoll-gradient-purified brain nonsynaptosomal mitochon

57 d by separation of epimastigote fractions on Percoll gradients in combination with Triton WR-1339 tre

58 mented with the peak organelle fraction into Percoll gradients in the presence of cytochalasin B and

59 gressive increase in density on self-forming Percoll gradients upon vesiculation and in vitro "aging.

60 Separation of epimastigote extracts on Percoll gradients yielded a dense fraction that containe

61 eam and procyclic trypomastigote extracts on Percoll gradients yielded fractions that contained H(+)-

62 r this study, immune cells were separated by Percoll gradients, and the resulting subpopulations were

63 anules separated by discontinuous sucrose or Percoll gradients, showed that CD14 was present in both

64 nd it involves separation over discontinuous percoll gradients.

65 nogold labeling and by their distribution on Percoll gradients.

66 ion followed by fractionation on sucrose and Percoll gradients.

67 ifferential centrifugation and discontinuous Percoll gradients.

68 pyrophosphatase activities were detected in Percoll-isolated chloroplasts and mitochondria from pea.

69 t with subcellular localization to plastids, Percoll-isolated chloroplasts from pea (Pisum sativum) s

70 fter hepatectomy was preserved only when the Percoll method was used.

71 se solution, containing Nycodenz, Ficoll, or Percoll (Pharmacia) that formed a density gradient that

72 d from healthy adult mouse liver by using a "Percoll-Plate-Wait" procedure.

73 Including a Percoll purification step; the entire procedure to seed

74 sociated with mitochondria in both crude and Percoll-purified "heavy" mitochondrial fractions (cRHM a

75 rformed on both preparations showed that the Percoll-purified granule preparation consisted of essent

76 on Percoll density gradients and compared to Percoll-purified in vitro-cultivated Leptospira (IVCL).

77 In Percoll-purified rat cerebrocortical synaptosomes, depol

78 Percoll-purified rat liver mitochondria exhibited a negl

79 tudy, a NOS was isolated to homogeneity from Percoll-purified rat liver mitochondria.

80 s macaque feces were purified by serial salt-Percoll-sucrose-iodixanol centrifugation, resulting in t