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1 y their interaction in vitro by coexpression/copurification.
2                                        Using copurification analysis and far-Western blotting, we fou
3 xistence of heterotrimers is implicated from copurification and crosslinking studies carried out in v
4                                              Copurification and Cys matching analyses suggest that se
5 hoproteomics and bioinformatics, followed by copurification and dephosphorylation assays.
6 d proteasome-interacting proteins by reverse copurification and immunoblotting experiments with and w
7                               Based on their copurification and intracellular distribution, vaults ma
8                                              Copurification and pull-down experiments showed that the
9                                              Copurification and two-hybrid studies showed that Scm3 a
10 ability to interact with UL5 as indicated by copurification and with UL8 as indicated by a supershift
11           Chemical cross-linking in vivo and copurification approaches established that YknX interact
12              Using both yeast two-hybrid and copurification approaches, we identified the protein-pro
13  and EpsL by functional characterization and copurification as well as coimmunoprecipitation.
14        We developed a novel Escherichia coli copurification assay to map the domain on the Drosophila
15                                    Using the copurification assay, we scanned this 28-amino-acid inte
16                   A combination of in vitro (copurification assays) and in vivo (bimolecular fluoresc
17  to the tail domain of KHC in two-hybrid and copurification assays, indicating that kinesin and UNC-7
18                            By two-hybrid and copurification assays, the DM3 mutant was found to be im
19 itro glutathione S-transferase pulldown, and copurification assays.
20    Coimmunoprecipitation and chromatographic copurification data suggest that pVHL-Cul2 complexes exi
21                                              Copurification experiments demonstrated that Ssa1p bound
22 required for cytochrome bd oxidase activity, copurification experiments indicate that CydX interacts
23                                              Copurification experiments indicated that the interactio
24 e DNA ratio for the two subunits was varied, copurification experiments indicated that the subunit st
25 modulin and TMEM16A could not be detected in copurification experiments or in functional assays.
26             To test this prediction, we used copurification experiments to identify five distinct and
27 h a WD40 repeat-containing protein, Cdh1, by copurification experiments.
28 A56/K2 and the EFC was demonstrated by their copurification from detergent-treated lysates of infecte
29  hypothesis, we describe herein the specific copurification from human placenta of 46- and 14-kDa pro
30                                      Here, a copurification-mass spectrometry approach was taken usin
31 oped in H. volcanii, allowing the successful copurification of (i) Hv7Sh with a histidine-tagged Hv54
32 a-sheet conformation can in part explain the copurification of A beta and apoE from AD amyloid plaque
33                    These results demonstrate copurification of a channel-associated G-protein that is
34 tors via a FLAG-tagged G subunit resulted in copurification of a Myc-tagged G subunit, implying more
35   Such an interaction was established by the copurification of A16 and G9 from infected cells under c
36 n vivo Reg1-Bmh interaction was confirmed by copurification of Bmh proteins with HA(3)-TAP-tagged Reg
37 t the N terminus, I5A, significantly reduced copurification of both ACBD3 and PI4KIIIbeta.
38                                          The copurification of calreticulin and endomannosidase from
39 rophyll recycling in a Ycf39-null mutant and copurification of chlorophyll synthase and unassembled D
40 s support this conclusion as demonstrated by copurification of coexpressed WT and L103A proteins in E
41 on affecting the T-loop of NifI(2) prevented copurification of dinitrogenase but did not affect copur
42                                              Copurification of eNOS with mitochondria was observed in
43          The identification was confirmed by copurification of enzyme activities, by similarities in
44  prevent deubiquitination after lysis or the copurification of interacting cofactors, this procedure
45 found that gE/gI are necessary for efficient copurification of KIF1A with Us9, especially at early ti
46  complex by using chemical cross-linking and copurification of LcrG and LcrV.
47                                              Copurification of MdtB and MdtC under these conditions s
48 rification of His-tagged NifI(2) resulted in copurification of NifI(1) and the dinitrogenase subunits
49 fication of dinitrogenase but did not affect copurification of NifI(1).
50 sion and affinity purification revealed that copurification of PI4KIIIbeta could be eliminated by mut
51 odepletion of the moesin kinase activity and copurification of PKC-theta with the enzymic activity.
52  hBH and UBC9 interacted in vivo by affinity copurification of proteins overexpressed in mammalian ce
53 nd absence of intact capsids and by affinity copurification of pU(L)17 and VP13/14 from lysates of ce
54                       Interestingly, we find copurification of Rad2 protein with TFIIH, such that TFI
55                                     Notably, copurification of RecA with DinB is somewhat enhanced in
56                                              Copurification of subunits II and III with aposubunit I
57                                              Copurification of the Aac2 protein with the TIM23 machin
58  the alpha(1)beta-proteasome resulted in the copurification of the alpha(2) protein with the alpha(1)
59 This strong association confers an effective copurification of the antigen with the starch fraction o
60 rnover of s-ODN in the brain, we studied the copurification of the immunoreactivity of biotin with bi
61 n between PKI and pPKR is indicated by their copurification on dsRNA agarose, despite evidence showin
62 dence for an interaction was provided by the copurification on immunoglobulin G-Sepharose of Nip7p wi
63                                              Copurification studies also identified physical interact
64                                              Copurification studies show that although Cpc2 and Ran1
65                                         Such copurification studies will provide insight into the sig
66 n vitro binding, as well as coexpression and copurification studies, gave evidence of CheA/CheS compl
67 and ColE1 by using cross-linking followed by copurification via histidine-tagged TolC.
68 y 600 kDa composed of six polypeptides whose copurification was completely dependent on the polyhisti
69 ing the in situ proximity ligation assay and copurifications, we show that the binding of Nck to the
70                          On the basis of its copurification with an SRB-containing RNA polymerase II
71 to identify the direct substrates of ClpC by copurification with ClpC(trap) followed by gel electroph
72 itin conjugation, polyubiquitin binding, and copurification with deubiquitinating enzymes.
73 combinant BHMT-2 that has been stabilized by copurification with human recombinant BHMT.
74 ith the cytosolic fraction, as documented by copurification with lactate dehydrogenase activity.
75                         We isolated Tic56 by copurification with Tandem Affinity Purification-tagged
76 ed protein because of its colocalization and copurification with the IF proteins desmin and vimentin
77 s as polymerase complex components (based on copurification with the polymerase activity and by coimm
78                  For RNA polymerase, reduced copurification with Tnp is observed in extracts from a t
79                                     Vimentin copurification with UPase was confirmed using both Weste
80 ochore localization, similar phenotypes, and copurification with xNdc80 and xNuf2.

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