ライフサイエンスコーパス: ultracentrifuge

1 ynamics of density gradient formation in the ultracentrifuge.

2 opseudomonas sphaeroides using an air-driven ultracentrifuge.

3 reparative scale equipment to the air-driven ultracentrifuge allows the rapid isolation of ICM vesicl

4 locity/equilibrium methods in the analytical ultracentrifuge and by immunoprecipitation using an anti

5 Equilibrium ultracentrifuge and circular dichroism (CD) studies of a

6 esulted in about 15 years of research on the ultracentrifuge and its application to the study of biol

7 sedimentation equilibrium in the analytical ultracentrifuge and model-independent SEDFIT-MSTAR analy

8 ssing MTP, HepG2 cells, and mouse liver were ultracentrifuged, and MTP was visualized in different de

9 cco mosaic virus led to our investigating an ultracentrifuge anomaly and the construction of a synthe

10 The mutant actin sediments in the analytical ultracentrifuge as a homogeneous monomeric species of 3.

11 d brain myosin V sediments in the analytical ultracentrifuge at 14 S as opposed to 11 S in the presen

12 Escherichia coli cells are centrifuged in an ultracentrifuge at high speed, 5-20% of the enzyme II ac

13 Plasma was ultracentrifuged at 17,000g for 60 minutes, and the micr

14 were adjusted to a density of 1.03 g/mL, and ultracentrifuged at 42,000 rpm and 37 degrees C for 13 h

15 luorescence detector for the XL-I analytical ultracentrifuge (AU-FDS) enables two different types of

16 ent sedimentation velocity in the analytical ultracentrifuge (AUC).

17 canning system of the Optima XL-I analytical ultracentrifuge can exhibit time-invariant noise compone

18 need to be excluded from the analysis due to ultracentrifuge cell end effects.

19 g also demonstrated formation of vesicles in ultracentrifuged Ch-unsaturated model bile (cholesterol

20 Sedimentation velocity in the analytical ultracentrifuge combined with calibrated gel chromatogra

21 Analytical ultracentrifuge data indicate that the hybrids have pred

22 S) that they are cleared from the analytical ultracentrifuge even at low speed (1500 rpm).

23 The far-UV CD and ultracentrifuge experiments, however, indicated relative

24 nder AU conditions) in the time frame of our ultracentrifuge experiments.

25 A new generation of compact, fast ultracentrifuges facilitates the rapid and fully informa

26 ydrates significantly decreased the size and ultracentrifuge flotation rate of the major LDL and the

27 romatography of biles (TC/(TC + EYPC) = 0.7) ultracentrifuged for various durations showed a progress

28 Velocity sedimentation in the analytical ultracentrifuge gave a single sedimenting species with a

29 and sedimentation velocity in the analytical ultracentrifuge glargine was shown to be primarily dimer

30 CAJ/Mnt mixtures were ultracentrifuged in order to separate them into supernat

31 apsed time in data files from the analytical ultracentrifuge, leading to overestimates of the sedimen

32 Ultracentrifuged material derived from sonicates of IFN-

33 We present a simple and fast ultracentrifuge method here for two platinum compounds a

34 Sedimentation equilibrium in the analytical ultracentrifuge of a dilute solution of protein (0.4 mg/

35 m HIV-infected individuals was collected and ultracentrifuged over 20% sucrose to isolate virions fro

36 Add-back of ultracentrifuge pellets (enriched in EVs but possibly ot

37 pol, and env regions of RNAs, prepared from ultracentrifuged pellets of filtered supernatants, indic

38 Ultracentrifuge results indicate the presence of three o

39 sedimentation equilibrium in the analytical ultracentrifuge (SEDFIT, SEDFIT-MSTAR and MULTISIG analy

40 oligomeric state of dynamin II by analytical ultracentrifuge sedimentation equilibrium measurements a

41 ng size exclusion chromatography, analytical ultracentrifuge sedimentation, circular dichroism, trans

42 g the UV absorption optics of the analytical ultracentrifuge.Selective monitoring of SinR in mixtures

43 n equilibrium measurements in the analytical ultracentrifuge show that both wild-type and C14S Sml1p

44 Analytical ultracentrifuge studies on Smad3 and Smad4 protein const

45 In addition, the SPI1-MSPalphabeta ultracentrifuge studies reveal a low abundance 2:2 compl

46 Analytical ultracentrifuge studies revealed that in solution, the r

47 lls isolated from ascites, and the cell-free ultracentrifuged supernatant.

48 tion of the Rayleigh interferometer onto the ultracentrifuge that had the greatest impact on our furt

49 n site was investigated using the analytical ultracentrifuge to analyze heterodimers formed from reco

50 sedimentation equilibrium in the analytical ultracentrifuge to describe self-association under nonid

51 This sample was ultracentrifuged to obtain a lipoprotein density distrib

52 Serial bronchoalveolar lavage specimens were ultracentrifuged to obtain the exosomal pellet for RNA e

53 rescence detection system for the analytical ultracentrifuge, we examined allosteric changes in PDE6

54 a recent study comparing various analytical ultracentrifuges, we showed that external calibration of

55 ation velocity experiments in the analytical ultracentrifuge were performed to identify different PAI

56 By equipping an analytical ultracentrifuge with a novel multi-wavelength detector,

57 and sedimentation velocity in the analytical ultracentrifuge with viscometry.