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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.
4                              Biochemical and co-purification analyses demonstrate that different CesA
5 evidences based on interaction conservation, co-purification and 3D domain contacts (iPfam, 3did).
6  single-stranded DNA-binding protein through co-purification and biochemical studies.
7                                              Co-purification and co-precipitation analyses demonstrat
8               For the first time, we show by co-purification and electron microscopy that mycobacteri
9  the pilus fibres, as measured using in vivo co-purification and in vitro pilus polymerization assays
10                                  As shown by co-purification and thermal inactivation studies, the 4'
11 med biochemically by co-immunoprecipitation, co-purification, and glutathione S-transferase pull-down
12 activity associated with CtBP/BARS is also a co-purification artefact.
13  in vitro electrophoretic mobility shift and co-purification assays.
14 eracts with ExsD in bacterial two-hybrid and co-purification assays.
15 ctrophoretic mobility gel shift analysis and co-purification assays.
16 hods employed included an overlay technique, co-purification, co-immunoprecipitation, and the use of
17                                              Co-purification experiments confirmed that LeuRS, LysRS,
18                                      Indeed, co-purification experiments indicate association of OsaC
19                                              Co-purification experiments of ChlB with Strep-ChlN sugg
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
22 igomeric CsgG complexes were confirmed using co-purification experiments.
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
25 polymerase (RNAP), we noticed the consistent co-purification of a 110-kDa polypeptide.
26 491)-affinity chromatography resulted in the co-purification of a member of the G12 family.
27               In this report, I describe the co-purification of a novel 70-kDa RNA helicase (RH70) an
28                                              Co-purification of AcrZ with AcrB, in the absence of bot
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
32                                              Co-purification of BMPs 2-7 with BMP1 prodomain sequence
33 ed enzymatic activities of GRP94 may reflect co-purification of contaminant enzymes, rather than intr
34                                      Namely, co-purification of different protein complexes as mediat
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
37                                          The co-purification of guanine nucleotide on the beta-tubuli
38  particles, and highly sensitive as shown by co-purification of homologues of the yeast pre-mRNA spli
39                   We recently documented the co-purification of members of the LIV-1 subfamily of ZIP
40 ay be at least partially responsible for the co-purification of NDP kinase with DnaK.
41                                              Co-purification of p110 with CK2 from Sf-9 cells that ov
42 ification of the unwinding activity revealed co-purification of P68 RNA helicase.
43 n studies were performed to test and compare co-purification of PCR inhibitors in samples extracted f
44    Pheromone induction greatly decreased the co-purification of PrgX.
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
52                  Bacterial co-expression and co-purification of the ERalpha/14-3-3zeta complex, follo
53 e receptor signaling complex was obtained by co-purification of the ethylene receptor ETR1 with a tag
54                                          The co-purification of the two polypeptides with transcripti
55 KAP 220 from rat testis extracts resulted in co-purification of the type II PKA holoenzyme.
56 ing (His)6-tagged p110 or p33 results in the co-purification of the well characterized p39 and p90 su
57                     Here we employed in vivo co-purification of tRNAs with endogenously expressed nuc
58                                              Co-purification of two different epitope-tagged forms of
59                                              Co-purification of Ung and Ndk through multicolumn low p
60 -tagged 54 kDa isoform (His54) were shown by co-purification on a Ni-NTA column to interact in Strept
61 en two proteins based on similarity of their co-purification patterns derived from MS data.
62                                      Using a co-purification strategy, we have identified a Ran GTPas
63                                              Co-purification studies demonstrate that SseA directly b
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
66           Pull down experiments completed by co-purification study prove that DauA and DctA interact
67                      Using co-expression and co-purification, we have been able to isolate a CaM-IQ m
68                        By performing protein co-purifications, we show that EspG(5) interacts with se
69 ursor is highly and specifically enriched by co-purification with at least two different small regula
70 ified ER as confirmed by co-fluorescence and co-purification with known ER proteins.
71 dentify novel telomerase regulators by their co-purification with the telomerase holoenzyme.
72                                  Here, using co-purification with TOC159 from Arabidopsis, we discove