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1 ize of <15 kDa by gel chromatography; and 4) native PAGE of AF yields a band of high apparent m.w., a
2                                 We adapted a native PAGE method to assess the formation and thermosta
3 mobility of the resulting RNP complexes in a native PAGE assay to determine which portions of these S
4 0-100% conversion of octamer to hexamer in a native PAGE mobility shift assay.
5 hese glycoproteins migrate as a complex in a native PAGE system.
6          Reaction stoichiometry analyses and native PAGE showed that for every factor Xa molecule inh
7 cattering, size exclusion chromatography and native PAGE show that Hs11S is assembled in different ol
8 ipitation, cross-linking, and denaturing and native PAGE analyses of Gal80 in vitro and fluorescence
9                    Pull-down experiments and native PAGE analysis indicated that the protein is both
10 activity, hydroxyl radical footprinting, and native PAGE.
11 crosomes because both isoelectrofocusing and native PAGE indicate the presence of a second region of
12  in mitoplasts and holo-CI by non-native and native PAGE, respectively, to determine their CI incorpo
13 inding, NMR titration, alanine scanning, and native PAGE.
14 -phase microextraction (SPME) GC-MS, SDS and native PAGE gel electrophoresis demonstrated that the ov
15           Analytical ultracentrifugation and native PAGE studies indicate that HSBP1 is predominantly
16 molecular mass estimated, using SDS-PAGE and native-PAGE electrophoresis, to be 86kDa.
17 ith high purity, as assessed by SDS-PAGE and native-PAGE zymogram, appearing as a single band of appr
18 redoxin (a-Fd) using UV-VIS spectroscopy and native-PAGE, as well as with a mitochondrial iron detect
19                                         Blue native PAGE analyses verify the presence of a SecYEG-Ppi
20                                         Blue native PAGE analysis demonstrates that RESC14 is essenti
21                                         Blue native PAGE analysis identified high molecular weight co
22                                         Blue native PAGE analysis indicates that native H complexes e
23                                         Blue native PAGE and FRET assays revealed 1% n-dodecyl beta-d
24                                         Blue native PAGE and immunoblot analysis revealed a single ba
25             Gel filtration analysis and blue native PAGE showed that Cbp1 is part of a single 900,000
26 ory chain proteins by Western blotting, blue native PAGE, and enzymatic activity assays revealed that
27 of cytochrome-c oxidase was detected by blue native PAGE, and interaction between subunit IV of cytoc
28                                Finally, blue native PAGE (BN-PAGE) revealed that under nondenaturing
29 A knockdowns, pharmacologic inhibitors, blue native PAGE, mass spectrometry, and assessment of mitoch
30 re resolved using two-dimensional PAGE (blue native PAGE and tricine/SDS/PAGE) and subsequent western
31                        Analyses by SEC, blue native PAGE, SDS-PAGE, and dynamic light scattering indi
32 sis of CI in Ndufs4(fky/fky) mice using blue native PAGE revealed the presence of a faster migrating
33 erization under native conditions using blue native PAGE.
34 probe IRE1alpha complexes in cells with blue native PAGE immunoblotting.
35                                         Blue native-PAGE analysis revealed defects in the organizatio
36  Western blot, immunoprecipitation, and Blue native-PAGE analysis.
37 e with ATR after cisplatin treatment by blue native-PAGE and co-immunoprecipitation.
38 ng of SCAP to INSIG-1, as determined by blue native-PAGE, and this is correlated with the inhibition
39  were observed in separate complexes by blue native-PAGE, the two proteins coimmunoprecipitated both
40   Following incubation at 47 degrees C, blue native-PAGE revealed a lower oligomeric form (alpha2beta
41 ted a large molecular weight complex in blue native-PAGE (~1.0 MDa), corresponding to the total molec
42 5 showed distinct migration patterns on blue native-PAGE.
43 ed into multiprotein complexes, we used blue native-PAGE (BN-PAGE) and cross-linking techniques to id
44                                         Blue-native PAGE analyses of intact oligomers and disulfide c
45                                         Blue-native PAGE analysis showed that the variant TatC protei
46 SRs with unprocessed 12S globulin by 2D blue-native PAGE/SDS-PAGE indicated that the nhx5 nhx6 knocko
47 ar vesicles and migrated as a trimer by blue-native PAGE.
48 , focusing on mammalian synapses we use blue-native PAGE and 'gene-tagging' of GluN1 to report the fi
49 ccurs when tafazzin is missing, we used blue-native PAGE and gene expression analysis to determine th
50 ometry (DIP-MS), which combines AP with blue-native-PAGE separation, data-independent acquisition wit
51                                           By native PAGE, formation of S-nitrosylated SP-D in vivo re
52                                           By native PAGE, it was possible to detect formation of a co
53 is moderate with high fidelity, confirmed by native PAGE, thermal transition study, and Ferguson anal
54 R are able to form a 1:1 complex detected by native PAGE.
55 nd single-stranded DNA, but as determined by native PAGE analysis, the protein cannot form a stable c
56  with (59)Fe-labeled transferrin followed by native PAGE electrophoresis.
57 ilibrium between these forms is indicated by native PAGE, which also reveals additional single-strand
58 tion of thylakoid complexes was performed by native PAGE and sucrose density centrifugation.
59 f the mass of the tRNA fragments resolved by native PAGE.
60 ic E5 channel stoichiometry was suggested by native PAGE studies.
61 rface was further validated both in vitro by native PAGE and in cellulo by cell-clustering and dendri
62  and analysis of the translation products by native-PAGE was used to study the maturation pathway of
63  monomeric by size exclusion chromatography, native PAGE, and small angle x-ray scattering.
64     Analytical ultracentrifugation and clear native PAGE analysis show that NRC is a stable pigment-p
65  from the membrane, are studied for coupling native PAGE with MALDI-MS.
66 E showed lower-than-expected mobility during native-PAGE, the largest hydrodynamic radius for the mon
67 naturing polyacrylamide gel electrophoresis (native PAGE) to have substantial decreases in their Mg2+
68                            Studies employing native PAGE suggest that most nDNA-encoded CI subunits f
69                              Gel filtration, native PAGE, and protein cross-linking were used to anal
70                                     However, native PAGE in gels containing amylopectin revealed that
71                         Immunoprecipitation, native PAGE, and functional studies confirmed that the G
72 ich comigrated with the protease activity in native PAGE and yielded multiple bands in SDS-PAGE under
73 0-kDa MP, which migrated as a single band in native PAGE.
74 S-PAGE showed that each of the bands seen in native PAGE was composed of several polypeptides.
75 emical and biophysical techniques, including native-PAGE, binding affinity by fluorescence anisotropy
76                      Off-line combination of native PAGE with MALDI-MS is demonstrated for high-resol
77  enhanced chemiluminescence visualization of native PAGE gels and through acrylamide fluorescence que
78 x had a total mass of 77 kDa and migrated on native PAGE at 75 kDa.
79 t to stabilize higher-order Bak oligomers on native PAGE, suggesting an important role in the Bak oli
80 n in P. aeruginosa cell lysates separated on native PAGE gels and stained for iron with Ferene S.
81 ws CA activity and is distinct from TWCA1 on native PAGE of radiolabeled T. weissflogii cell lysates.
82 igrated at their monomer molecular weight on native PAGE.
83  A single prominent protein band appeared on native-PAGE and SDS-PAGE implying that the mPPO is a mon
84 urified trypsin appeared as a single band on native-PAGE.
85 wever, upon anion-exchange chromatography or native PAGE, CT separates from the BC and BCCP subunits
86 nge chromatography and analyzed by SDS-PAGE, native PAGE, and Western immunoblot analysis.
87                                     Parallel native PAGE, immunoblotting and Complex I activity assay
88 r dichroism spectroscopy, thermal stability, native PAGE, and analytical ultracentrifugation indicate
89     These results highlight the power of the native PAGE assay for membrane protein biochemistry and
90 ch adopt multiple conformations according to native PAGE.
91 mutagenesis, analytical ultracentrifugation, native PAGE, and activity assays, we found that these co
92  enzyme using denaturing SDS-PAGE but, under native PAGE conditions, was not observed to form the app
93                                      We used native PAGE to follow the activity of Cif from the human
94  of the ZPI-binding interface, together with native PAGE and kinetic analyses of PZ binding to ZPI, t