ライフサイエンスコーパス: protein sequencing

1 to be monitored and charted without gene or protein sequencing.

2 ectrophoresis followed by mass spectrometric protein sequencing.

3 leavage sites were mapped through N-terminal protein sequencing.

4 come a key technology for modern large-scale protein sequencing.

5 l followed by Northwestern hybridization and protein sequencing.

6 conformation stability assay, and N-terminal protein sequencing.

7 me, which was proven to be BAP by N terminus protein sequencing.

8 ignificantly increase the speed of automated protein sequencing.

9 ion and S-alkylation, mass spectrometry, and protein sequencing.

10 ytical ultracentrifugation, and quantitative protein sequencing.

11 s, two of which were supported by N-terminal protein sequencing.

12 ditions and identified by mass spectrometric protein sequencing.

13 ous nuclear ribonucleoprotein L (hnRNP L) by protein sequencing.

14 owing this technique's potential for de novo protein sequencing.

15 namel matrix and characterized it by partial protein sequencing.

16 ights of 13 and 15 kDa, are characterized by protein sequencing.

17 g, electrospray mass spectrometry, and Edman protein sequencing.

18 ss spectrometry, and mass spectrometry-based protein sequencing.

19 Cys113, Cys195, and Cys421, respectively, by protein sequencing after modification with [1-14C]iodoac

20 Protein sequencing and antibody supershift experiments i

21 Surprisingly, protein sequencing and antibody supershift experiments i

22 e fragments were characterised by N-terminal protein sequencing and electrospray mass spectrometry.

23 r proline makes GP-II an attractive tool for protein sequencing and identification of stably folded d

24 In this report, we show by protein sequencing and immunoreactivity that the fourth

25 e of the truncated forms of TSLP using Edman protein sequencing and matrix-assisted laser desorption/

26 To minimize low-quantity sample handling for protein sequencing and matrix-assisted laser desorption/

27 e report here by the criteria of the partial protein sequencing and subsequent cDNA cloning that glyc

28 After purification, protein sequencing and Western blotting, the endopeptida

29 peed, directness, sensitivity, and ease over protein sequencing and Western-blotting methods and hold

30 (MN) by high-pressure liquid chromatography, protein sequencing, and amino acid analyses determined a

31 ion was measured by ELISA, Western blotting, protein sequencing, and chemotaxis assays.

32 yzed by high-pressure liquid chromatography, protein sequencing, and immunoblotting.

33 Isolation, protein sequencing, and immunoprecipitation identified t

34 chromatography, light scattering, N-terminal protein sequencing, and sedimentation velocity.

35 el electrophoresis and subjected to internal protein sequencing, and the sequence of five peptides wa

36 Using the RNA expression and protein sequencing assay (REAP-seq), we quantified prote

37 e protein structure represent a challenge in protein sequencing by tandem MS (MS/MS).

38 opossum amelogenins through a combination of protein sequencing, cloning, and DNA sequencing.

39 Western blots and protein sequencing data indicate that an IGHD3-encoded p

40 Protein sequencing established the identity of the recep

41 N-terminal protein sequencing established the presence of leader pe

42 Subsequent peptide mass fingerprinting and protein sequencing experiments confirmed the dimeric for

43 with an endoribonuclease activity; however, protein sequencing failed to detect the NCL.

44 Direct protein sequencing, followed by gene cloning, revealed a

45 dimensional electrophoresis, electroblotting/protein sequencing, high performance liquid chromatograp

46 For allergen identification protein sequencing, homology search and mass spectrometr

47 ot promoter fragment, followed by N-terminal protein sequencing, identified the SarA and SarR protein

48 Protein sequencing in combination with mutagenesis ident

49 re routinely being generated by DNA, RNA and protein sequencing in the genomic era.

50 Western blotting and amino-terminal protein sequencing indicated that all lysine residues in

51 herefore, the development of single-molecule protein sequencing is a critical step in the search for

52 De novo protein sequencing is essential for understanding cellul

53 uccess of mass spectrometry (MS) for de novo protein sequencing, Leu and Ile have been generally cons

54 aracterized by a combination of NH2-terminal protein sequencing, mass spectrometry, and mass spectrom

55 Protein sequencing of an internal 61-kDa proteolytic fra

56 Protein sequencing of fragments isolated from proteolyti

57 Classical biochemical purification and protein sequencing of highly purified fractions containi

58 Protein sequencing of proteolyzed tetanus toxin C fragme

59 onal protein gel electrophoresis (2-DGE) and protein sequencing of select target proteins.

60 for the purification of soluble dMAG and by protein sequencing of short peptides containing the carb

61 Tryptic digestion and subsequent protein sequencing of the [8-3H]BDDFHA-labeled enzyme re

62 Following protein sequencing of the isolated approximately 45 kDa

63 Protein sequencing of the p68, p34, and p25 polypeptide

64 We report here partial protein sequencing of the rod delta subunit and isolatio

65 NH2-terminal protein sequencing of the two bands revealed identity wi

66 Protein sequencing of tryptic peptides of the 57-kDa com

67 phosphorylation, phosphopeptide mapping, and protein sequencing of VR1 cytoplasmic domains delineate

68 ted biochemical fractionation and subsequent protein sequencing on a grand scale to identify individu

69 We have plotted our progress in protein sequencing over the last two decades and found t

70 Amino-terminal protein sequencing, peptide fingerprinting, and immunoch

71 N-Terminal protein sequencing proved that DIDS treatment created AE

72 Protein sequencing provided the basis for determination

73 TAR RNA and Tat protein fragment by RNA and protein sequencing, respectively.

74 Our immunoblot and protein sequencing results on treated virions showed tha

75 Analysis by mass spectrometric protein sequencing revealed a DNA-dependent protein kina

76 Protein sequencing revealed that CAP is derived from the

77 Protein sequencing revealed that the microcystin-bound p

78 Protein sequencing showed that propofol inhibited to the

79 ght-dependent manner, where epitope tags and protein sequencing showed that the NCL was excised from

80 Immunofluorescence, immunoprecipitation, and protein sequencing studies identified the target antigen

81 her development as a novel rapid, label-free protein sequencing technique.

82 r internal peptide sequences using different protein sequencing techniques, and using the resulting s

83 Here, we propose a new technique for de novo protein sequencing that involves translocating a polypep

84 We have shown by Western blot analysis and protein sequencing that the 105-kDa polypeptide is sigma

85 by shotgun proteomics involves digesting the proteins, sequencing the resulting peptides by data-depe

86 from toxin transcripts, without resorting to protein sequencing, the propeptide cleavage site in the

87 In this study, protein sequencing was used to identify the PK cleavage

88 his was confirmed by limited proteolysis and protein sequencing, which showed increased protection of