1 Glutathione S-transferase pulldown and
far Western analyses demonstrate that the interaction al
2 As assessed by
far Western analyses TraM interacts with TraR by directl
3 Both
far-western analyses and immuno-pull-down assays indicat
4 Using protein-protein pull-down and
far-Western analyses, we further show that the presence
5 ng to cellular proteins based on large-scale
far-western analyses.
6 tion of apoJ/XIP8 with Ku70 was confirmed by
far-western analyses.
7 tly with MLH1 in the yeast-two hybrid assay;
far Western analysis and co-immunoprecipitations confirm
8 measured in the absence of poly(A) RNA using
far Western analysis and confirmed by direct fluorescenc
9 We have used
Far Western analysis and phosphopeptide competition assa
10 Far Western analysis and the rebinding interaction with
11 s sequence (MRPFL) was shown to bind PCNA by
far Western analysis and to compete with p50 for binding
12 Far Western analysis demonstrated a direct association b
13 A trimeric
far Western analysis demonstrated the formation of a ter
14 Far Western analysis of N- and C-terminal deletion mutan
15 Far Western analysis revealed that PELP1 interacts with
16 Far Western analysis revealed that ZO-2 can directly bin
17 Far Western analysis reveals that SHP-2, via its Src hom
18 Far Western analysis shows that eIF3-p44 interacts stron
19 In
Far Western analysis, 29 distinct proteins were identifi
20 Coimmunoprecipitation,
far Western analysis, and glutathione S-transferase bind
21 a human placenta cDNA expression library by
Far Western analysis.
22 lated p62(DOK) was bound by SHP-1 C453S in a
far Western analysis.
23 osphorylated by RSK and used as ligands in a
far Western analysis; only those containing Ser(P)(703)
24 d in vitro to isolated denatured keratins in
Far-Western analysis and to native IFs in pull-down assa
25 umulation along the nuclear periphery and in
far-Western analysis bound to proteins which comigrated
26 nteracted with apobec-1 was also detected by
far-Western analysis in the eluate from the wild-type RN
27 Far-Western analysis suggests increased phosphorylation
28 In the current work, we performed
Far-Western analysis to identify PfPP2C substrates.
29 Using the yeast two-hybrid system and
far-Western analysis, we verified the importance of this
30 squito Pfs47 receptor protein (P47Rec) using
far-Western analysis.
31 gion in protein interactions was verified by
Far-Western analysis.
32 PCNA-binding motif was shown to bind PCNA by
far-Western analysis.
33 Furthermore, "
far Western"
analysis suggested that the largest subunit
34 In
far western and northern North America, the host reservo
35 MG-I, as modified by casein kinase II, using
far Western and protein-protein interaction solution ass
36 nd does so via a direct interaction based on
Far Western and reverse Far Western blotting.
37 We confirmed LOX-PL interactions using
far Western and solid phase binding assays.
38 1 and AP-1 was demonstrated both in vitro by
Far-Western and antibody pulldown assays with recombinan
39 Far-Western and MS analyses identified both well-establi
40 phosphorylated PDGFR from control cells in a
Far Western assay.
41 SF/SF2 using a yeast two-hybrid system and a
far Western assay.
42 Glutathione S-transferase pull-down and
far Western assays showed that ADP-ribosylated Crk-I or
43 ides in both immunoprecipitation and reverse
Far Western assays.
44 Far-Western assays demonstrated that PKBalpha-mediated S
45 Co-immunoprecipitation,
Far-Western assays, and two-hybrid assays showed that TI
46 0-kDa protein homologous with SRC-1/TIF2, by
far-Western-
based expression screening.
47 the GST pulldown, co-immunoprecipitation and
far-western binding assays.
48 tein experiments, coimmunoprecipitations and
Far Western blot analyses to demonstrate direct binding
49 Far Western blot analysis also indicated that the SH3 do
50 Far Western blot analysis confirmed the specific binding
51 Far Western blot analysis confirms that SAPK/JNK binds d
52 Coimmunoprecipitation assays and
far Western blot analysis demonstrate that this mutation
53 xperiments, subsequent studies using reverse
Far Western blot analysis demonstrated that only the car
54 quiescent cells is probably not direct since
Far Western blot analysis did not reveal the binding of
55 Moreover,
Far Western blot analysis identified at least three AKAP
56 Far Western blot analysis implicates A190 of Pol I as we
57 Far Western blot analysis suggested that the tandem SH2
58 Far Western blot analysis was used to demonstrate the bi
59 Far Western blot analysis with either Nck, the SH2 domai
60 eningitidis strains was detected by FACS and
Far Western blot analysis, and occurred in the absence o
61 This binding was confirmed by
Far Western blot analysis, sedimentation on a glycerol g
62 type 3 (CR3, CD11b/CD18) was used to probe a
Far Western blot of a detergent extract of Hc cell wall
63 recognized by DC, VLA-5 was used to probe a
Far Western blot of a yeast freeze/thaw extract (F/TE) t
64 interact tightly and specifically, both on a
far Western blot of yeast vacuolar proteins and in the y
65 wild-type but not kinase-inactive JAK2 in a
far Western blot.
66 Real-time polymerase chain reaction, (
far) Western blot, immunoprecipitation, and immunocytoch
67 the domain of VP2 required for binding VP1,
far-Western blot analyses using a series of truncated VP
68 Here we used
far-Western blot analysis and microscale thermophoresis
69 Far-Western blot analysis established that HMW1B interac
70 to bind only to the beta-subunit of eIF2 by
far-Western blot analysis.
71 Structure-function analyses using
far-Western blot and transient cotransfection assays rev
72 on of PCSK9 activity, and we demonstrated by
far-Western blot assay that the M1 and M2 domains are ne
73 A was detected with the yeast two-hybrid and
far-Western blot assays.
74 C10258 (MFn8, Lsa66), and LIC10537 (MFn9) by
far-Western blot assays.
75 o I in enzyme-linked immunosorbent assay and
far-Western blot assays.
76 the pea aphid, Acyrthosiphon pisum, using a
far-Western blot method.
77 xible competitive binding assay based on the
far-Western blot technique, in which a battery of Src ho
78 ith Ace from OG1RF mutanolysin extracts on a
far-Western blot.
79 A protein (
far Western)
blot analysis revealed that dTAFIII105, pre
80 ombinant Fg chains and truncation mutants in
Far Western blots and solid-phase binding assays.
81 size from 120 to 200 kDa were identified on
Far Western blots for their ability to bind pTP.
82 Comparative
far Western blots have shown that hTAF(II)135 interacts
83 Using the peptides as probes in
far Western blots showed direct binding of the phosphory
84 ation experiments with knockdown of GAB2 and
Far-Western blots proved the direct interaction of SHP2
85 In "
far Western"
blots of mouse embryonic protein extracts,
86 Binding assays and
far Western blotting analysis demonstrated association o
87 Binding assays and
far Western blotting analysis, using glutathione S-trans
88 Far Western blotting and two-hybrid analyses detect a di
89 Far Western blotting revealed the presence of an approxi
90 ELISA and
Far Western blotting showed that recombinant vimentin bo
91 Far Western blotting showed that this interaction was li
92 Moreover,
far Western blotting using platelet membrane proteins re
93 Far Western blotting with a CRKL-SH3 glutathione S-trans
94 acts directly with DNA polymerase beta using
far Western blotting, affinity precipitation and yeast t
95 PAK2 with CIN85 SH3 domains was confirmed by
Far Western blotting.
96 interaction based on Far Western and reverse
Far Western blotting.
97 Using
far-Western blotting analysis of chemically cleaved and
98 Furthermore,
far-Western blotting analysis shows that SopE directly i
99 n HPV type 11 (HPV-11) E1-binding protein by
far-Western blotting and by microsequence analyses of a
100 The
far-Western blotting and co-immunoprecipitation assays d
101 In
far-Western blotting and guanine nucleotide saturation s
102 Initially, using a combination of
far-western blotting and phosphoCTD affinity chromatogra
103 By
Far-Western blotting and yeast two-hybrid assay, we demo
104 To test this hypothesis, we performed EYS
Far-Western blotting assay and generated pomgnt1 mutant
105 Far-Western blotting detected interaction of SATB1 and C
106 Far-Western blotting identified proteins of 150 and 240
107 sociates to amplify its functional capacity,
far-Western blotting of cholangiocyte epithelial cell pr
108 Far-Western blotting of EBP50 isolated by two-dimensiona
109 Interacting protein partners indicated by
far-Western blotting were confirmed by immunoprecipitati
110 By
far-Western blotting, and verified by coimmunoprecipitat
111 in-binding assay (VOPBA) in combination with
far-Western blotting, gradient-purified EAV particles we
112 phosphorylation by quantitative Western and
far-Western blotting, mass spectrometry, and computation
113 Using copurification analysis and
far-Western blotting, we found that Asp2 and Asp3 could
114 t binding to the NM could be demonstrated by
far-Western blotting.
115 ne, immunoprecipitation, immunoblotting, and
far-Western blotting.
116 action of VirB9 and VirB6-2 was confirmed by
far-Western blotting.
117 and LAT upon CRP stimulation of platelets by
far-Western blotting.
118 nd that comigrated with that detected by pTP
far-Western blotting.
119 system was in contrast to a strong signal by
far-Western blotting.
120 ): 1) phospho-specific mass spectrometry; 2)
far-Western blotting; and 3) live cell single-molecule i
121 Using interaction "
Far Western"
blotting assays, we systematically tested f
122 rom 20 community forest user groups in three
far-western districts, we applied the structural equatio
123 teract with Sp1 in vitro as analyzed by West(
far)-Western,
electrophoretic mobility shift assay-super
124 However, immunoprecipitation and
far-western experiments identified the chromophorylated
125 obo groups of inferred Central, Western, and
Far-Western geographic origin within the bonobo range.
126 isted during early domestication, one at the
far western (
Iberia) and the other at the far eastern ra
127 mited, and have only been available from the
far western Maghreb (Morocco)(1-3).
128 hat-GTPgammaSN terminus was analyzed using a
far Western method for examining Galphat-GTPgammaS prote
129 Using
Far Western overlay assay, we have identified additional
130 Far-Western overlays of soluble extracts of cauliflower
131 C terminus (C1aB) was first identified via a
far-Western peptide screen and used to create a prothera
132 We have used
Far Western screening and in vitro interaction assays to
133 Far Western/
solid phase assays established TINag binding
134 shown by mammalian two-hybrid, pulldown, and
far Western studies.
135 munoprecipitation, quantitative imaging, and
far-Western studies with cells expressing wild type, as
136 polyclonal or C3b monoclonal antibodies in a
far-Western technique followed by mass spectroscopy to i
137 Using a
Far Western type of analysis, we detected several potent
138 e disease), in Ixodes pacificus ticks of the
far-western United States.
139 Far Westerns with digoxigenin-conjugated protein phospha
140 her co-immunoprecipitation experiments or in
Far Westerns with the SH2 domains of these two proteins.
141 e demonstrated by surface plasmon resonance,
far-western,
yeast two-hybrid, recombinant- and native-c