ライフサイエンスコーパス: 2D gel electrophoresis

1 tion with the FF-IEF system over traditional 2D gel electrophoresis.

2 immunohistochemistry, Western blotting, and 2D gel electrophoresis.

3 mirror repeat tracts from PKD1 intron 21 by 2D gel electrophoresis.

4 d proteomes (designated sub-proteomes) using 2D gel electrophoresis.

5 4 h before labeling with [35S]methionine and 2D gel electrophoresis.

6 isplayed weak origin activity as detected by 2D gel electrophoresis.

7 entification of proteins separated by 1D and 2D gel electrophoresis.

8 etermined by densitometry analysis on 1D and 2D gels electrophoresis.

9 infection was separated by two-dimensional (2D) gel electrophoresis.

10 re previously identified by two-dimensional (2D) gel electrophoresis.

11 as determined previously by two-dimensional (2D) gel electrophoresis.

12 eparated by high-resolution two-dimensional (2D) gel electrophoresis.

13 inal proteins were separated by SDS-PAGE and 2D gel electrophoresis (2-DE) and sera from AR patients

14 jority of proteomic investigations still use 2D gel electrophoresis (2-DE) with immobilized pH gradie

15 The gel filtration and 2D gel electrophoresis analysis showed a significant red

16 -labeled islet proteins were separated using 2D gel electrophoresis and analyzed using the BioImage c

17 iates using a combination of neutral agarose 2D gel electrophoresis and electron microscopy.

18 A TG pollen extract was analyzed by 2D gel electrophoresis and IgE/IgG immunoblots using poo

19 sine phosphorylation were investigated using 2D gel electrophoresis and immunoblots probed with an an

20 s study demonstrates that the combination of 2D gel electrophoresis and mass spectrometry is a powerf

21 Using 2D gel electrophoresis and mass spectrometry, we have id

22 (10 ng/ml) or DHT (10(-8) M) for 24 h before 2D gel electrophoresis and Western immunoblotting with a

23 We combined 2D gel electrophoresis and whole genome approaches to ma

24 examined yeast proteins by two-dimensional (2D) gel electrophoresis and gathered quantitative inform

25 Two-dimensional (2D) gel electrophoresis and mass spectrometry (MS) have

26 sed a proteomic approach of two-dimensional (2D) gel electrophoresis and mass spectrometry (MS) to id

27 (IEF) is the first step for two-dimensional (2D) gel electrophoresis and plays an important role in s

28 mining the substrate for denitrase combining 2D-gel electrophoresis and an on-blot enzyme assay.

29 Using fluorescent derivatives, 2D gel electrophoresis, and MS, we established that PACM

30 n, SDS-PAGE and HPLC, MALDI-TOF MS analysis, 2D gel electrophoresis, and phosphospecific antibodies.

31 le colonic biopsies were characterized using 2D-gel electrophoresis, and peptide mass fingerprinting

32 ll established, was analyzed by quantitative 2D gel electrophoresis followed by mass spectrometry (MS

33 and IgE-reactive proteins were identified by 2D gel electrophoresis, followed by Western blot with po

34 Further analysis using the 2D gel electrophoresis implied that the labeled protein

35 A method for carrying out 2D gel electrophoresis in a capillary format is presente

36 ical regulatory and signaling mechanisms and 2D gel electrophoresis is able to resolve many PTM-induc

37 Using high-resolution 2D gel electrophoresis, mass spectrometry, and immunoblo

38 nt BMC and a number of empty BMC variants by 2D-gel electrophoresis, mass spectrometry, transmission

39 y candidate proteins, we applied a sensitive 2D gel electrophoresis method to quantify protein differ

40 udied using gel filtration, two-dimensional (2D) gel electrophoresis, multi-angle light scattering, c

41 Similarly, both S1 nuclease and 2D gel electrophoresis of DNA topoisomers did not detect

42 ically generated NO on protein expression by 2D gel electrophoresis of neonatal rat islet samples.

43 e yield of stalk material shed and performed 2D gel electrophoresis of purified stalks and cellular f

44 Two-dimensional (2D) gel electrophoresis, single telomere-length analysis

45 esponding plasma fraction were studied using 2D gel electrophoresis techniques.

46 n assay and demonstrated by two-dimensional (2D) gel electrophoresis that all of the intermediates co

47 We have applied 2D gel electrophoresis to analyze the extent, nature, an

48 f complex protein mixtures, two-dimensional (2D) gel electrophoresis was combined with in-gel MAAH, a

49 s activated by E2 in brain, two-dimensional (2D) gel electrophoresis was conducted to screen the mito

50 By 2D gel electrophoresis, we detect two different kinds of

51 By mass spectrometry and 2D gel electrophoresis, we identified several peptides w

52 eins are first separated by two dimensional (2D) gel electrophoresis, Western blotted onto poly(vinyl

53 ing a nonbiased proteomic approach combining 2D gel electrophoresis with in-gel proteolysis, peptide

54 the proteins were extracted and analyzed by 2D gel electrophoresis with subsequent in-gel digestion.