ライフサイエンスコーパス: two-dimensional electrophoresis

1 ns from rat liver homogenate and resolved by two-dimensional electrophoresis.

2 rom 14-week cultures, was examined by use of two-dimensional electrophoresis.

3 ristics from wild type AR as determined with two-dimensional electrophoresis.

4 rms are active in glial tumors by performing two-dimensional electrophoresis.

5 PK2 was followed by protein separation using two-dimensional electrophoresis.

6 isoelectric point of PrP quasispecies under two-dimensional electrophoresis.

7 s NZ131 rgg and NZ131 speB were separated by two-dimensional electrophoresis.

8 f alpha-migrating particles as determined by two-dimensional electrophoresis.

9 arative electrophoresis, electroelution, and two-dimensional electrophoresis.

10 grown in 5% CO2 and in air were examined by two-dimensional electrophoresis.

11 cross the growth range were examined through two-dimensional electrophoresis (2-D gels) of the proteo

12 Two-dimensional electrophoresis (2-DE) and matrix-assist

13 Cabernet) in order to obtain a separation by two-dimensional electrophoresis (2-DE) compatible with m

14 Proteins were separated by two-dimensional electrophoresis (2-DE), visualized by fl

15 Although two-dimensional electrophoresis (2D-GE) remains the basi

16 g (IEF) with subsequent gel electrophoresis, two-dimensional electrophoresis (2DE) affords more speci

17 Solubilization of membrane proteins for two-dimensional electrophoresis (2DE) is very difficult.

18 Immunoblotting of proteins separated by two-dimensional electrophoresis (2DE) with sera from mic

19 mination of normal H-Ras, K-Ras and N-Ras by two-dimensional electrophoresis after exposure to bacter

20 aration of thousands of cellular proteins by two-dimensional electrophoresis allows the detailed comp

21 tivariate analysis, a total of 63 spots from two-dimensional electrophoresis analysis and 135 protein

22 Two-dimensional electrophoresis analysis of B. burgdorfe

23 linked to Hap1 repression and activation by two-dimensional electrophoresis analysis.

24 acted from seeds and pulp juice, resolved by two dimensional electrophoresis and major spots subjecte

25 y 150 soluble root proteins were resolved by two-dimensional electrophoresis and analyzed by MALDI-To

26 dipocyte proteins were separated by one- and two-dimensional electrophoresis and approximately 60 2SC

27 We have resolved the labeled proteins using two-dimensional electrophoresis and autofluorography.

28 ualized using metabolic labeling followed by two-dimensional electrophoresis and fluorography.

29 Soluble thylakoid proteins were separated by two-dimensional electrophoresis and identified by mass s

30 xtreme proteolysis indices were separated by two-dimensional electrophoresis and identified by tandem

31 Two-dimensional electrophoresis and immunoblot of adhesi

32 Two-dimensional electrophoresis and MALDI-TOF mass spect

33 By using two-dimensional electrophoresis and mass spectrometry (m

34 The protein was identified as HSP60 using two-dimensional electrophoresis and mass spectrometry an

35 ells, we used a proteomic approach involving two-dimensional electrophoresis and mass spectrometry to

36 Two-dimensional electrophoresis and mass spectrometry we

37 s of innovations in the core technologies of two-dimensional electrophoresis and mass spectrometry, a

38 in E. coli minicells using a combination of two-dimensional electrophoresis and mass spectrometry.

39 melanocyte versus melanoma cell lines using two-dimensional electrophoresis and mass spectrometry.

40 Two-dimensional electrophoresis and matrix-assisted lase

41 om hearts subjected to coronary occlusion by two-dimensional electrophoresis and subsequent matrix-as

42 ith CRHSP-28 in rat acini following one- and two-dimensional electrophoresis and underwent a marked a

43 oduce a large number of species separable by two-dimensional electrophoresis and which we have propos

44 The 6C5-H4CA antigen was resolved by two-dimensional electrophoresis, and a partial protein s

45 sing high performance liquid chromatography, two-dimensional electrophoresis, and immunoblotting with

46 arget of EGCG using affinity chromatography, two-dimensional electrophoresis, and mass spectrometry f

47 We used immunoprecipitation, one- and two-dimensional electrophoresis, and mass spectrometry t

48 Outer membrane proteins were separated by two-dimensional electrophoresis, and proteins recognized

49 ce liquid chromatography (HPLC) and one- and two-dimensional electrophoresis, and the 3H label was de

50 re, performing further protein separation by two-dimensional electrophoresis, and utilizing mass spec

51 Using highly sensitive two-dimensional electrophoresis-based proteomics, we ide

52 the protein, as determined by a pI shift on two-dimensional electrophoresis, but 14-3-3zeta dimeriza

53 free glutathione and identified by one- and two-dimensional electrophoresis coupled with mass spectr

54 ved by the cumulative time-resolved emission two-dimensional electrophoresis (CuTEDGE) technology fac

55 Two-dimensional electrophoresis demonstrated that Kelch

56 Two-dimensional electrophoresis demonstrated that produc

57 Consistent with these modifications, two-dimensional electrophoresis demonstrated that SWP3 h

58 Further analysis by two-dimensional electrophoresis demonstrated three const

59 50 S subunit via a proteomic approach using two-dimensional electrophoresis, electroblotting/protein

60 andmark genomic scanning (RLGS) is a type of two-dimensional electrophoresis employed in the genome-w

61 Two-dimensional electrophoresis followed by immunoblotti

62 y SDS-polyacrylamide gel electrophoresis and two-dimensional electrophoresis followed by Western immu

63 Analysis by two-dimensional electrophoresis following in vivo phosph

64 lation by wild-type and E381A mutant ExoS by two-dimensional electrophoresis found the former to ADP-

65 ystematic comparison of 634 protein spots in two-dimensional electrophoresis gels across five experim

66 ation steps (reverse-phase HPLC and one- and two-dimensional electrophoresis gels), different enzymat

67 rved to migrate to multiple protein spots on two-dimensional electrophoresis gels.

68 abeled proteins are isolated by conventional two-dimensional electrophoresis: (i) nonreducing/reducin

69 rometric analysis of the changes observed in two-dimensional electrophoresis identified a number of p

70 Urine proteins were separated by two-dimensional electrophoresis in 32 patients with FSGS

71 High-resolution two-dimensional electrophoresis in combination with the

72 in conjugates (50 to >200 kDa; pI 5.3-6.8 by two-dimensional electrophoresis) in bovine rod outer seg

73 aphic purification of greater than 400-fold, two-dimensional electrophoresis indicated that the strom

74 Two-dimensional electrophoresis is a critical technique

75 n recognition and quantification in one- and two-dimensional electrophoresis is demonstrated for bioa

76 To resolve the cartilage proteins by two-dimensional electrophoresis, it was necessary to rem

77 Using two-dimensional electrophoresis, mass spectrometry, immu

78 ns by using two complementary methodologies, two-dimensional electrophoresis/mass spectrometry and li

79 We used two-dimensional electrophoresis (nonequilibrium pH gradi

80 Two-dimensional electrophoresis of bovine lens zeta-crys

81 data obtained from combinations of one- and two-dimensional electrophoresis of completely or partial

82 by trypsin and by immunoblot analysis after two-dimensional electrophoresis of isolated lysosomes an

83 Two-dimensional electrophoresis of rat heart alphaB-crys

84 fects on DNA replication were analyzed using two-dimensional electrophoresis of replication intermedi

85 dently mutated to an alanine and analyzed by two-dimensional electrophoresis; only serine 4 was phosp

86 Two-dimensional electrophoresis provided evidence that t

87 lization of Toxoplasma secretory products by two-dimensional electrophoresis revealed approximately 1

88 Two-dimensional electrophoresis revealed that PMA treatm

89 on in complex samples are also applicable to two-dimensional electrophoresis separations.

90 s, we constructed a high-voltage, automatic, two-dimensional electrophoresis system and used this in

91 A novel two-dimensional electrophoresis system to be carried out

92 Using two-dimensional electrophoresis, the extracellular prote

93 s in combination with thinner gels to reduce two-dimensional electrophoresis time about 80%.

94 The two-dimensional electrophoresis was used for analysis of

95 Western analysis after two-dimensional electrophoresis was used to measure the

96 g by (35)S and by (14)C combined with native/two-dimensional electrophoresis, we assessed the synthes

97 Using two-dimensional electrophoresis, we demonstrate a struct

98 Subcellular fractionation and two-dimensional electrophoresis were used in conjunction

99 ned medium released by PMNs were resolved by two-dimensional electrophoresis with immobilized pH grad

100 We used two-dimensional electrophoresis with mass spectrometry t