ライフサイエンスコーパス: native polyacrylamide gel electrophoresis

1 ion by immunohistochemical analysis and blue native polyacrylamide gel electrophoresis.

2 he same rate as the wild-type AcrB trimer in native polyacrylamide gel electrophoresis.

3 en holo-Shp and holo-HtsA was examined using native polyacrylamide gel electrophoresis.

4 upercomplex that can be displayed using blue native polyacrylamide gel electrophoresis.

5 d zone of activity in the stacking gel after native polyacrylamide gel electrophoresis.

6 erized by analytical ultracentrifugation and native polyacrylamide gel electrophoresis.

7 esolved by gel permeation chromatography and native-polyacrylamide gel electrophoresis.

8 ed both by size exclusion chromatography and native polyacrylamide gel electrophoresis a third hybrid

9 The samples are resolved by native polyacrylamide gel electrophoresis, after which f

10 on of thylakoids post cross linking and blue-native polyacrylamide gel electrophoresis analysis shows

11 responsible for this enhanced reactivity, a native polyacrylamide gel electrophoresis analysis was c

12 ion desorption mass spectrometry and by blue native polyacrylamide gel electrophoresis analysis.

13 taining, a cellulose binding experiment, and native polyacrylamide gel electrophoresis analysis.

14 Blue native-polyacrylamide gel electrophoresis analysis showe

15 Blue Native polyacrylamide gel electrophoresis, analytical ul

16 Further, using native polyacrylamide gel electrophoresis and a yeast tw

17 Small angle X-ray scattering, native polyacrylamide gel electrophoresis and activity a

18 Native polyacrylamide gel electrophoresis and analytical

19 previously unidentified A-minor junctions by native polyacrylamide gel electrophoresis and atomic for

20 Results from blue native polyacrylamide gel electrophoresis and chemical c

21 Two-dimensional blue native polyacrylamide gel electrophoresis and coimmunopr

22 homomultimerization in vivo was obtained by native polyacrylamide gel electrophoresis and gel filtra

23 Native polyacrylamide gel electrophoresis and glycerol g

24 haracterized these protein complexes by blue native polyacrylamide gel electrophoresis and identified

25 Native polyacrylamide gel electrophoresis and mass spect

26 In this study, we use native polyacrylamide gel electrophoresis and one-dimens

27 and side-by-side double rings, as judged by native polyacrylamide gel electrophoresis and scanning t

28 ant, and chimeric ORF50 proteins, using Blue Native polyacrylamide gel electrophoresis and size exclu

29 oxin A and toxin B exhibited single bands on native polyacrylamide gel electrophoresis and two peptid

30 0 Inuit women (18-39 years old) by combining native-polyacrylamide gel electrophoresis and liquid chr

31 detected by circular dichroism spectroscopy, native polyacrylamide gel electrophoresis, and enzyme-li

32 ion-exchange chromatography, gel filtration, native polyacrylamide gel electrophoresis, and two subst

33 dynamic and quasi-elastic light scattering, native polyacrylamide gel electrophoresis, and ultracent

34 twork architecture at the molecular level by native polyacrylamide gel electrophoresis, as well as th

35 The results of a native polyacrylamide gel electrophoresis assay using JR

36 ines and disrupted NPM oligomer formation by native polyacrylamide gel electrophoresis assay.

37 The structures have been characterized by native polyacrylamide gel electrophoresis, atomic force

38 ccessfully achieved by a combination of blue-native polyacrylamide gel electrophoresis (BN-PAGE) for

39 PSI-LHCI-LHCII supercomplex isolated by blue native polyacrylamide gel electrophoresis (BN-PAGE) from

40 Blue native polyacrylamide gel electrophoresis (BN-PAGE) has

41 Analysis of PP2A and PP4 complexes by blue native polyacrylamide gel electrophoresis (BN-PAGE) indi

42 Blue native polyacrylamide gel electrophoresis (BN-PAGE) is a

43 lized size exclusion chromatography and blue native polyacrylamide gel electrophoresis (BN-PAGE) to d

44 We also report the application of Blue Native polyacrylamide gel electrophoresis (BN-PAGE), a h

45 ecipitation and one- or two-dimensional blue native polyacrylamide gel electrophoresis (BN-PAGE).

46 ence of the ESSS subunit as revealed by blue native polyacrylamide gel electrophoresis (BN/PAGE) anal

47 at liver mitochondria were subjected to blue native polyacrylamide gel electrophoresis (BNGE) to sepa

48 Native polyacrylamide gel electrophoresis experiments sh

49 Immunoprecipitation and blue native polyacrylamide gel electrophoresis, followed by i

50 Blue native polyacrylamide gel electrophoresis, gel filtratio

51 erties of thylakoid preparations directly in native polyacrylamide gel electrophoresis gels, enabling

52 Blue native polyacrylamide gel electrophoresis identified PCF

53 vitro to form a holotoxin, as determined by native polyacrylamide gel electrophoresis immunoblotting

54 charomyces cerevisiae subjected to colorless native polyacrylamide gel electrophoresis in the presenc

55 Analytical gel filtration and native polyacrylamide gel electrophoresis indicate that

56 Gel filtration chromatography and native polyacrylamide gel electrophoresis indicated that

57 Native polyacrylamide gel electrophoresis indicated that

58 Native polyacrylamide gel electrophoresis is a powerful

59 Upon native polyacrylamide gel electrophoresis, moreover, oli

60 Native polyacrylamide gel electrophoresis of blood sampl

61 r aminopeptidases (APs) were separated using native polyacrylamide gel electrophoresis of cell-free e

62 Blue Native polyacrylamide gel electrophoresis of T. brucei m

63 Native polyacrylamide gel electrophoresis of the affinit

64 Blue native-polyacrylamide gel electrophoresis of mitochondri

65 Native polyacrylamide gel electrophoresis (PAGE) analysi

66 strategy has been proven to be successful by native polyacrylamide gel electrophoresis (PAGE) and cry

67 Both native polyacrylamide gel electrophoresis (PAGE) and por

68 -dimensional analysis, the mobility shift in native polyacrylamide gel electrophoresis (PAGE) due to

69 Native polyacrylamide gel electrophoresis (PAGE) gel shi

70 Native polyacrylamide gel electrophoresis (PAGE) was int

71 ture dependent data were obtained by SDS and native polyacrylamide gel electrophoresis (PAGE), differ

72 The enzyme was further purified by native-polyacrylamide gel electrophoresis (PAGE) and aff

73 ein mobility shift assay was devised using a native polyacrylamide gel electrophoresis protocol to ex

74 in) transition from tetramer to monomer, and native polyacrylamide gel electrophoresis provided addit

75 Size-exclusion chromatography and blue native polyacrylamide gel electrophoresis revealed a mod

76 Native polyacrylamide gel electrophoresis showed that th

77 equilibration analysis, circular dichroism, native polyacrylamide-gel electrophoresis, size exclusio

78 Using two-dimensional Blue Native polyacrylamide gel electrophoresis/sodium dodecyl

79 Blue native polyacrylamide gel electrophoresis studies reveal

80 s I, III, IV, and V were isolated using Blue Native polyacrylamide gel electrophoresis techniques.

81 Native polyacrylamide gel electrophoresis was used to an

82 Blue native polyacrylamide gel electrophoresis was used to is

83 Native polyacrylamide gel electrophoresis was used to pr

84 -linking, size exclusion chromatography, and native polyacrylamide gel electrophoresis, we demonstrat