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1 nd protein kinases, as determined by protein microsequencing.
2 d through photoaffinity labeling and protein microsequencing.
3 ach band were analyzed by mass spectrometric microsequencing.
4 age, the purified proteins were suitable for microsequencing.
5 fied by gel electrophoresis and subjected to microsequencing.
6 s of the Sec6-Sec8-Sec15 complex for peptide microsequencing.
7 ng over 70 amino acids identified by peptide microsequencing.
8 ]halothane, and subjected to proteolysis and microsequencing.
9 e first 10 amino acids determined by protein microsequencing.
10 should be compatible with both MALDI-TOF and microsequencing.
11 (35)S-labeled C2GnT-M was established using microsequencing.
12 ure liquid chromatography and amino-terminal microsequencing.
13 een isolated and subjected to amino-terminal microsequencing.
14 ed from the retina, was confirmed by protein microsequencing.
15 be authentic betaB(2)-crystallin by protein microsequencing.
16 ere identified by phosphopeptide mapping and microsequencing.
17 acting proteins by affinity purification and microsequencing.
18 f three N-terminal residues, as confirmed by microsequencing.
19 protein by affinity purification and peptide microsequencing.
20 s of three tryptic peptides were obtained by microsequencing.
21 ed, purified, and finally subjected to Edman microsequencing.
22 tides were analyzed by mass spectrometry and microsequencing.
25 ermination, endoglycosidase sensitivity, and microsequencing analysis as a porcine homologue of CD58.
28 s band was subsequently shown by Western and microsequencing analysis to comprise both the carboxylas
29 terminal amino acid sequence was obtained by microsequencing analysis, and full-length clones were ob
31 tide mapping, site-directed mutagenesis, and microsequencing analysis, we identified two major sites
34 cleavage sites were identified by N-terminal microsequencing and electrospray mass spectrometry, and
36 Analysis of the phosphopeptides by automated microsequencing and manual Edman degradation identified
37 hoto-cross-linking in TnC were determined by microsequencing and mass spectrometry following enzymati
38 ross-linking site for both TnC mutants using microsequencing and mass spectrometry following proteoly
39 Carcinus maenas, was determined by automated microsequencing and MS, and was almost identical to that
41 itory protein that was identified by peptide microsequencing and protein database analysis as troponi
47 bioactive and intermediate CART molecules by microsequencing and/or high performance liquid chromatog
48 Both proteins were identified by peptide microsequencing, and a complementary DNA encoding the hi
49 ization tandem mass spectrometry, N-terminal microsequencing, and immunoblotting with specific antibo
53 eins labeled in this assay was identified by microsequencing as HSP25, purified as a recombinant prot
54 using 2-dimensional gels and amino-terminal microsequencing as one of a select few [35S]methionine p
55 and its identification by mass spectrometry microsequencing as pregnancy-associated plasma protein-A
56 To this end we purified and identified via microsequencing ATF2 as a major URE- bound and CREB-asso
58 s were identified from tryptic digests using microsequencing by tandem mass spectrometry and database
59 Structures were established by NH2-terminal microsequencing, cross-link analysis, electrospray mass
60 s, direct [(14)C]halothane photolabeling and microsequencing demonstrated dominant labeling of W9, le
61 subunits on analytical SDS-PAGE, and protein microsequencing establishes that the GABA(A)R-modulating
62 Purified LRBP was subjected to N-terminal microsequencing followed by homology search, which revea
63 The results obtained from fragmented protein microsequencing have suggested that autocrine motility f
64 novel mass spectrometry strategy and peptide microsequencing identified 33 known proteins, many of wh
73 rmined using epitope-defined antibodies, and microsequencing indicated that K18 cleavage occurs at a
75 ry analysis of peptide fragments and peptide microsequencing, indicates that Cdc37 is comprised of th
76 ve the following primary structures by Edman microsequencing: IWLTALKFLGKHAAKHLAKQQLSKL-NH2 for lycot
77 e VP16 activation domain followed by peptide microsequencing led to the identification of ARC92 as a
82 protein, caveolin-2, was identified through microsequencing of adipocyte-derived caveolin-enriched m
83 ify of the purified protein was confirmed by microsequencing of an endoproteinase glutamic acid-C fra
102 d sequences with those obtained from peptide microsequencing of the purified complex components.
104 n (KuAg) as documented by partial amino acid microsequencing of tryptic digests and immunologic react
107 hich were successfully identified by protein microsequencing or matrix-assisted laser desorption ioni
111 unoaffinity purification of this protein and microsequencing revealed homology to sheep CD58 as well
117 ize exclusion chromatography, and subsequent microsequencing revealed that they are the zeta isoform
118 beads from the library and subjected them to microsequencing, revealing the sequence of the unreacted
124 ing of Nef function, we used biochemical and microsequencing techniques to isolate and identify Nef-a
126 we demonstrated by protein purification and microsequencing that ribosomes of maize (Zea mays L.) co
128 minus was determined for the beta-subunit by microsequencing the protein purified from etiolated maiz
129 liquid chromatography, together with protein microsequencing, the protein was identified as heregulin
131 rain) G2 and G1 proteins were established by microsequencing to be equivalent to aa 525 and 1046, res
132 lypeptides (12, 32 and 38 kDa) were found by microsequencing to be identical to parts of the predicte
133 ely with two polypeptides that were shown by microsequencing to be the alpha- and beta-subunits of Ac
135 olypeptide was purified and shown by peptide microsequencing to be the Torpedo ortholog of the small
136 esent in this construct and was subjected to microsequencing to confirm its identity and the site of
137 It is now routine using automatic Edman microsequencing to determine the primary structure of pe
140 l I-like ectodomain followed by SDS-PAGE and microsequencing using electrospray (ISI-Q-TOF-Micromass)
142 nous moesin, which was identified by peptide microsequencing, was dependent on phosphatidylglycerol (
143 ed by [(3)H]AziPm were identified by protein microsequencing, we found propofol-inhibitable photolabe
144 ombination of mutational analysis and direct microsequencing, we have determined that this cysteine p
146 protein was subjected to tryptic mapping and microsequencing, which was followed by molecular cloning
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