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1 PAK2 with CIN85 SH3 domains was confirmed by Far Western blotting.
2 interaction based on Far Western and reverse Far Western blotting.
3 and LAT upon CRP stimulation of platelets by far-Western blotting.
4 nd that comigrated with that detected by pTP far-Western blotting.
5 system was in contrast to a strong signal by far-Western blotting.
6 t binding to the NM could be demonstrated by far-Western blotting.
7 ne, immunoprecipitation, immunoblotting, and far-Western blotting.
8 action of VirB9 and VirB6-2 was confirmed by far-Western blotting.
9 acts directly with DNA polymerase beta using far Western blotting, affinity precipitation and yeast t
10                           Binding assays and far Western blotting analysis demonstrated association o
11                           Binding assays and far Western blotting analysis, using glutathione S-trans
12                                        Using far-Western blotting analysis of chemically cleaved and
13                                 Furthermore, far-Western blotting analysis shows that SopE directly i
14                                              Far Western blotting and two-hybrid analyses detect a di
15 n HPV type 11 (HPV-11) E1-binding protein by far-Western blotting and by microsequence analyses of a
16                                          The far-Western blotting and co-immunoprecipitation assays d
17                                           In far-Western blotting and guanine nucleotide saturation s
18            Initially, using a combination of far-western blotting and phosphoCTD affinity chromatogra
19                                           By Far-Western blotting and yeast two-hybrid assay, we demo
20                                           By far-Western blotting, and verified by coimmunoprecipitat
21 ): 1) phospho-specific mass spectrometry; 2) far-Western blotting; and 3) live cell single-molecule i
22    To test this hypothesis, we performed EYS Far-Western blotting assay and generated pomgnt1 mutant
23                           Using interaction "Far Western" blotting assays, we systematically tested f
24                                              Far-Western blotting detected interaction of SATB1 and C
25 in-binding assay (VOPBA) in combination with far-Western blotting, gradient-purified EAV particles we
26                                              Far-Western blotting identified proteins of 150 and 240
27  phosphorylation by quantitative Western and far-Western blotting, mass spectrometry, and computation
28 sociates to amplify its functional capacity, far-Western blotting of cholangiocyte epithelial cell pr
29                                              Far-Western blotting of EBP50 isolated by two-dimensiona
30                                              Far Western blotting revealed the presence of an approxi
31                                    ELISA and Far Western blotting showed that recombinant vimentin bo
32                                              Far Western blotting showed that this interaction was li
33                                    Moreover, far Western blotting using platelet membrane proteins re
34            Using copurification analysis and far-Western blotting, we found that Asp2 and Asp3 could
35    Interacting protein partners indicated by far-Western blotting were confirmed by immunoprecipitati
36                                              Far Western blotting with a CRKL-SH3 glutathione S-trans