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1 fic proteins and we confirmed two of them by co-purification.
2 ed by co-immunoprecipitation and/or in vitro co-purification.
3 tatistical noise inherent in observations of co-purifications.
5 evidences based on interaction conservation, co-purification and 3D domain contacts (iPfam, 3did).
9 the pilus fibres, as measured using in vivo co-purification and in vitro pilus polymerization assays
11 med biochemically by co-immunoprecipitation, co-purification, and glutathione S-transferase pull-down
16 hods employed included an overlay technique, co-purification, co-immunoprecipitation, and the use of
20 -C from individual subunits was derived from co-purification experiments performed with various combi
21 ts of mass spectrometry results from protein co-purification experiments, yeast two-hybrid interactio
23 By several independent criteria, including co-purification, immunoprecipitation, and gel filtration
24 e co-immunoprecipitation of the proteins and co-purification in the glutathione S-transferase (GST) p
29 e found that this motif is essential for the co-purification of all four CLSYs with Pol IV, but that
30 Isolation of this protein resulted in the co-purification of another unique protein called heat re
31 tubulin was suggested by the following: (i) co-purification of betaARK with tubulin from brain tissu
33 ed enzymatic activities of GRP94 may reflect co-purification of contaminant enzymes, rather than intr
35 DDeltaD3 from M. acetivorans resulted in the co-purification of endogenous subunit L with each tagged
36 ith other ethylene receptors was obtained by co-purification of ETR1 with tagged versions of ERS1, ET
38 particles, and highly sensitive as shown by co-purification of homologues of the yeast pre-mRNA spli
43 n studies were performed to test and compare co-purification of PCR inhibitors in samples extracted f
45 of constitutive proteasome complexes and the co-purification of proteasomes with aggregation-prone su
46 with similar properties demonstrated precise co-purification of protein recognized by all antibodies
47 nes without use of detergents and observed a co-purification of PspA, a membrane-stress response prot
48 ciated with NDP kinase from all tissues, but co-purification of pyruvate kinase was seen only in live
49 from yeast nuclear extracts resulted in the co-purification of Rad1, Rad7, Rad10, Rad16, Rad23, RPA,
50 ibosomal protein fused to a tag for affinity co-purification of ribosomes and the mRNAs that they are
51 ired for its association with CTR1, based on co-purification of tagged ETR1 mutants and CTR1 after ex
53 e receptor signaling complex was obtained by co-purification of the ethylene receptor ETR1 with a tag
56 ing (His)6-tagged p110 or p33 results in the co-purification of the well characterized p39 and p90 su
60 -tagged 54 kDa isoform (His54) were shown by co-purification on a Ni-NTA column to interact in Strept
64 ination of gel filtration chromatography and co-purification studies demonstrates that SBP2 does not
65 electrophoretic mobility shift assays and co-purification studies showed that Rep-(1-160) did not
69 ursor is highly and specifically enriched by co-purification with at least two different small regula