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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
16 -labeled islet proteins were separated using 2D gel electrophoresis and analyzed using the BioImage c
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
22 (10 ng/ml) or DHT (10(-8) M) for 24 h before 2D gel electrophoresis and Western immunoblotting with a
24 examined yeast proteins by two-dimensional (2D) gel electrophoresis and gathered quantitative inform
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
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
36 ical regulatory and signaling mechanisms and 2D gel electrophoresis is able to resolve many PTM-induc
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
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
46 n assay and demonstrated by two-dimensional (2D) gel electrophoresis that all of the intermediates co
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
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.
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