1 are specific for spermatogenesis between the
two hybrids.
2 Yeast
two-hybrid analyses showed that 4E02 targets A. thaliana
3 Yeast
two-hybrid analyses showed that RD21A interacts with mul
4 s actually binds to ankyrin-G, both in yeast
two-hybrid analysis and by coimmunoprecipitation in situ
5 nascent PG processing in vivo, and bacterial
two-hybrid analysis identified an MltG-PBP1b interaction
6 Bacterial
two-hybrid analysis identified several interactions of P
7 oteome, we carried out a comprehensive yeast
two-hybrid analysis of all the putative proteins encoded
8 Two-hybrid analysis revealed that the dynamins are part
9 Yeast
two-hybrid analysis reveals that SIX6OS1 interacts with
10 Yeast
two-hybrid analysis showed no evidence of a direct inter
11 Yeast
two-hybrid analysis shows that the rod domain of KRT1 in
12 Affinity purification and pairwise yeast
two-hybrid analysis suggest that ZC3H5 forms a complex w
13 Here, we used bacterial
two-hybrid analysis to identify a surface-exposed alpha-
14 We used yeast (Saccharomyces cerevisiae)
two-hybrid analysis to map the binding site of Bud23 on
15 A yeast
two-hybrid analysis uncovered the actin-depolymerizing f
16 hat disrupted the interaction, as assayed by
two-hybrid analysis, did not display a growth defect.
17 diate this electrostatic interaction using a
two-hybrid analysis.
18 ay crystallography, electron microscopy, and
two-hybrid analysis.
19 with the PAK kinase Ste20 and MAPKK Ste7 by
two-hybrid analysis.
20 vel binding partner of E5, YIPF4 using yeast
two-hybrid analysis.
21 ns to measure interactions, that complements
two-hybrid and affinity-purification techniques.
22 Yeast
two-hybrid and bimolecular complementation fluorescence
23 deacetylase subunits were observed in yeast
two-hybrid and bimolecular fluorescence assays, consiste
24 protein interaction studies including yeast
two-hybrid and Bimolecular Fluorescence Complementation
25 Furthermore, yeast
two-hybrid and bimolecular fluorescence complementation
26 Yeast
two-hybrid and bimolecular fluorescence complementation
27 Yeast
two-hybrid and bimolecular fluorescence complementation
28 In yeast (Saccharomyces cerevisiae)
two-hybrid and bimolecular fluorescence complementation
29 In this study, using membrane yeast
two-hybrid and bimolecular fluorescence complementation
30 Protein-protein interaction studies (yeast
two-hybrid and bimolecular fluorescence complementation)
31 GRMZM2G035341 and GRMZM2G152328) using yeast
two-hybrid and bimolecular fluorescent complementation a
32 Yeast
two-hybrid and biochemical studies have revealed that th
33 Results from yeast
two-hybrid and co-expression in Escherichia coli confirm
34 Yeast
two-hybrid and co-immunoprecipitation assays demonstrate
35 We demonstrate, using bacterial
two-hybrid and coimmunoprecipitation assays, that endoge
36 s cAMP's effects on NCC, and conducted yeast
two-hybrid and coimmunoprecipitation experiments in NCC-
37 Analysis of interactions using the bacterial
two-hybrid and cross-linking assays showed that TraE and
38 Bacterial
two-hybrid and gene-reporter assays demonstrated that Fs
39 (an E3 ubiquitin ligase), as shown by yeast
two-hybrid and in vitro pulldown assays.
40 nsiderably higher than that of proteome-wide
two-hybrid and mass spectrometry screens.
41 Using yeast
two-hybrid and mass-spectrometric analysis, we report th
42 cing" (DoMY-Seq), which leverages both yeast
two-hybrid and next-generation sequencing techniques.
43 Two-hybrid and pulldown assays demonstrated that UL20, b
44 therian and avian cDNA libraries using yeast-
two-hybrid and split-ubiquitin systems.
45 Yeast
two-hybrid and subsequent in silico structural predictio
46 Transcriptional assays, such as yeast
two-hybrid and TANGO, that convert transient protein-pro
47 DDBH2) domains, with contradicting bacterial
two-hybrid and yeast two-hybrid studies suggesting that
48 Modeling, yeast
two-hybrid,
and functional data reveal that this PF2-lik
49 coimmunoprecipitation, colocalization, yeast
two-hybrid,
and small interfering RNA (siRNA) analyses.
50 In the current study, we have used a yeast
two-hybrid approach to identify unknown partners of p22p
51 on with DCTN6 were mapped by a reverse yeast
two-hybrid approach using a randomly mutated E2 library.
52 In this study, a yeast
two-hybrid approach using the cytoplasmic domain of TfR2
53 ms and identify putative substrates, a yeast
two-hybrid approach was carried on and a protein was ide
54 TolA-pIII complex, we developed a bacterial
two-hybrid approach, named Oxi-BTH, suited for studying
55 Using a genetic
two-hybrid approach, we demonstrate that LpqN interacts
56 By using the Yeast
Two-Hybrid approach, we identified a disintegrin and met
57 Using a yeast
two-hybrid approach, we identified the 5'-3' exonuclease
58 We used proteomic and yeast
two-hybrid approaches to elucidate host factors involved
59 nity purification-mass spectrometry or yeast
two-hybrid approaches.
60 de, extended-peptide, and protein levels and
two "hybrid"
approaches (i.e., protein calibrator with S
61 By a combination of yeast-
two hybrid assay, in vitro binding, and coimmunoprecipit
62 Bacterial
two-hybrid assay and accumulation of Gp0.6 only in MreB-
63 interact with Hsp90Ecin vivo in a bacterial
two-hybrid assay and in vitro in a bio-layer interferome
64 e in ClpB interaction in vivo in a bacterial
two-hybrid assay and in vitro in a fluorescence anisotro
65 ns also directly interact in vivo in a yeast
two-hybrid assay and in vitro through ammonium sulfate c
66 reliminary experiments involving a bacterial
two-hybrid assay are presented that corroborate the exis
67 A split-ubiquitin membrane yeast
two-hybrid assay demonstrated specific interactions of t
68 The yeast
two-hybrid assay identified that proteasome subunit alph
69 Yeast
two-hybrid assay results indicated that MKT1 directly in
70 Furthermore, results of the mammalian
two-hybrid assay showed that cyclin-dependent kinase 3 (
71 ssisted RNA-RNA-binding protein [RBP] yeast)
two-hybrid assay to assess binding of our CEH mutant RNA
72 addressed this question using the bacterial
two-hybrid assay to determine how the initiation protein
73 reened a kidney cDNA library through a yeast
two-hybrid assay using NKCC2 C terminus as bait.
74 h deletion analysis, co-immunoprecipitation,
two-hybrid assay, and pulldown assays with expressed pro
75 ructure was corroborated using the bacterial
two-hybrid assay, biochemical characterization of the pu
76 ions with core exocyst subunits in the yeast
two-hybrid assay, cytoplasmic localization, and genetic
77 We searched for such proteins by yeast
two-hybrid assay, using GARP as a bait to screen a human
78 Using a modified version of the mammalian
two-hybrid assay, we demonstrate that the interaction st
79 Utilizing a yeast
two-hybrid assay, we discovered several novel interactor
80 Using the above-mentioned
two-hybrid assay, we found that zebrafish Tmc1 and Tmc2a
81 modulate its function, we performed a yeast
two-hybrid assay.
82 subunits including Sgf29 and Spt7 in a yeast
two-hybrid assay.
83 racting proteins were screened using a yeast
two-hybrid assay.
84 at prevent DEPTOR binding to mTOR in a yeast-
two-hybrid assay.
85 proteins were identified by a modified yeast
two-hybrid assay.
86 high-throughput, array-based, directed yeast
two-hybrid assay.
87 ing proteins with GLP-1R by a membrane yeast
two-hybrid assay.
88 was further confirmed by Co-IP and mammalian
two-hybrid assay.
89 ck proteins, Hsp16.9 and Hsp17.5, in a yeast
two-hybrid assay.
90 PYL6 and MYC2 interact in yeast
two hybrid assays and the interaction is enhanced in the
91 Site-directed mutagenesis and yeast-
two hybrid assays identified DnaA and DnaN binding sites
92 In yeast-
two hybrid assays, ORRM3 interacts with RIP1, ORRM2 and
93 e ESCRT-III-related proteins CHMP1A in yeast
two hybrid assays.
94 ters, subcellular localization and bacterial
two hybrid assays.
95 ABD1 directly interacts with ABI5 in yeast
two-hybrid assays and associates with ABI5 in vivo by co
96 Yeast
two-hybrid assays and coimmunoprecipitation experiments
97 and TMC1 or TMC2 was observed in both yeast
two-hybrid assays and coimmunoprecipitation experiments.
98 o the blue-light photoreceptor FKF1 in yeast
two-hybrid assays and delays flowering in Arabidopsis wh
99 r the interaction of CRY2 with COP1 in yeast
two-hybrid assays and in planta Mutations in the VP moti
100 with beta-catenin was confirmed using yeast
two-hybrid assays and in vitro synthesized proteins.
101 Mammalian
two-hybrid assays demonstrated that PB selectively incre
102 Yeast
two-hybrid assays established a direct interaction of Ce
103 cular fluorescence complementation and yeast-
two-hybrid assays indicated that the IDR3 domain does no
104 Yeast
two-hybrid assays involving seven ABA receptor proteins
105 Yeast
two-hybrid assays reveal that RgsD can interact with the
106 Furthermore, our yeast
two-hybrid assays show that MoVps17 and MoVps5 can inter
107 -seq and proteomics data together with yeast
two-hybrid assays suggest that MS23 along with MS32, bHL
108 Yeast
two-hybrid assays suggested that GID1a has the highest a
109 ass spectrometry, split-luciferase and yeast-
two-hybrid assays to generate a single reliability score
110 we used membrane-based split ubiquitin yeast
two-hybrid assays to identify novel GLP1R interactors in
111 Yeast
two-hybrid assays were used to identify ABA signaling co
112 tion of pull-downs, mass spectrometry, yeast
two-hybrid assays, and chemical genomics, we demonstrate
113 In yeast
two-hybrid assays, FgMcm1 interacted with Mat1-1-1 and F
114 with P. blakesleeanus Ras homologs in yeast
two-hybrid assays, indicating that MadC is a regulator o
115 amily member periplakin, identified in yeast
two-hybrid assays, interacted with a membrane-proximal d
116 In yeast
two-hybrid assays, MAS2 interacted with splicing and rib
117 fatty acid synthase II (FAS-II) in bacterial
two-hybrid assays, suggesting essentiality may be linked
118 Here we show that in yeast
two-hybrid assays, the non-EAR protein, Related to ABI3/
119 and thermal shift assays, and membrane yeast
two-hybrid assays, to define the mechanism mediating thi
120 ntaining plastidial proteins in binary yeast
two-hybrid assays, we also gained insights into the spec
121 ion of cross-linking/affinity pull-downs and
two-hybrid assays, we determined that TraK self-associat
122 Using yeast
two-hybrid assays, we determined the interactions among
123 und state failed to bind to AvrL567 in yeast
two-hybrid assays, while binding was detected to the sig
124 an interact with both TTI1 and TTI2 in yeast
two-hybrid assays.
125 h the CAR ligand-binding domain in mammalian
two-hybrid assays; and 5) disrupts CAR binding to the pr
126 zation and subcellular localization by yeast
two-hybrid,
bimolecular fluorescence complementation and
127 By using yeast-
two-hybrid,
bimolecular fluorescence complementation and
128 In this study,
two hybrid biochemical routes combining lignin chemical
129 Using yeast
two-hybrid,
biochemical, and cellular assays, we determi
130 Conversely, protein-level and the
two hybrid calibrations achieved good quantitative accur
131 r surface to UVF's thermostability, we built
two hybrid,
chimeric proteins combining the sets of buri
132 offspring phenotypes suggest the presence of
two hybrid classes, F1s and var. incana backcrosses, as
133 tic approaches, physiological methods, yeast
two-hybrid,
co-immunoprecipitation, and chromatin immuno
134 binding partner of IL-13Ralpha2 using yeast
two-hybrid,
co-immunoprecipitation, co-localization and
135 Yeast
two-hybrid,
coimmunoprecipitation and bimolecular fluore
136 size exclusion chromatography, and bacterial
two-hybrid data revealed that PilM forms dimers mediated
137 Furthermore, yeast
two-hybrid data showed that CPTL2 and CPT3 interact.
138 Bacterial
two-hybrid data suggested the connectivity of the cytopl
139 d be assembled with GAA and TTC strands; the
two hybrid duplexes [r(GAA):d(TTC) and d(GAA):r(UUC)] in
140 xperiments, chemical crosslinking, bacterial
two-hybrid experiments and nuclear magnetic resonance ch
141 Yeast
two-hybrid experiments confirmed the direct interaction
142 Two-hybrid experiments demonstrate self-interaction of t
143 Yeast
two-hybrid experiments identified PG core proteins ABC1K
144 Yeast
two-hybrid experiments indicate that the interaction of
145 Follow-up bacterial
two-hybrid experiments suggest additional contacts creat
146 Yeast
two-hybrid experiments suggested that the phosphorylatio
147 ognition Nexus (MORN) domain; previous yeast
two-hybrid experiments with full-length and MORN-truncat
148 and IAA7 in yeast (Saccharomyces cerevisiae)
two-hybrid experiments, indicating that these proteins w
149 tory subunits of PP2A, Wdb and Wrd, in yeast
two-hybrid experiments.
150 Two hybrid fluorinated double-chain surfactants with a d
151 Using bacterial
two-hybrid,
gel filtration, and MS analyses, we demonstr
152 erase pulldown, coimmunoprecipitation, yeast
two-hybrid,
gel shift, and chromatin immunoprecipitation
153 Using a yeast
two-hybrid genome-wide screen, we identified novel inter
154 pha-helix(656-666), which are required for a
two-hybrid Gln3-Tor1 interaction, also abolished rapamyc
155 Using yeast
two-hybrid,
GST pull-down, co-immunoprecipitation and bi
156 ary methods-a high-throughput enhanced yeast
two-hybrid (
HT-eY2H) assay and a mammalian-cell-based Ga
157 s between the various MORF proteins by yeast
two-hybrid,
in vitro pulldown, and bimolecular fluoresce
158 Yeast-
two-hybrid interaction and complementation assays indica
159 The most widely used
two-hybrid interaction assay for proteins involved in en
160 sis, site-directed mutagenesis and bacterial
two-hybrid interaction studies, indicate an evolutionary
161 omato immune induced complementary DNA yeast
two-hybrid library and screened it with Me10 as bait.
162 G's mechanism of action, we screened a yeast
two-hybrid library for P. falciparum proteins that inter
163 Using a yeast (Saccharomyces cerevisiae)
two-hybrid library of S. reilianum-infected maize tissue
164 Screening a yeast
two-hybrid library revealed that UNC-89 interacts with p
165 Here, we screened a yeast
two-hybrid library using the Arabidopsis LDAP3 isoform a
166 We screened a yeast
two-hybrid library using the central domain of ubiquilin
167 ouple to each resonant cavity mode, yielding
two hybrid light-matter (polariton) modes and a reservoi
168 we utilized the bacterial adenylate cyclase
two-hybrid method and carried out a saturation mutagenes
169 rall prediction accuracy, with the in-silico
two-hybrid method contributing most to performance.
170 re, we present a massively multiplexed yeast
two-hybrid method, CrY2H-seq, which uses a Cre recombina
171 Here, we demonstrate by yeast
two-hybrid method, immunoprecipitation assays, and surfa
172 sequence-based prediction methods: in-silico
two-hybrid,
mirror-tree, gene fusion, phylogenetic profi
173 species, we show that selfish centromeres in
two hybrid mouse models use the same molecular pathway b
174 Sho1p PPIs through the use of membrane yeast
two-hybrid (
MYTH), an assay specifically suited to ident
175 We have engineered a novel NanoLuc
two-hybrid (
N2H) system that integrates 12 different ver
176 The volatile profile of
two hybrids of "Radicchio di Chioggia", Corelli and Bott
177 es associated with ontologic cancer sets and
two hybrids of separate experimental replicates clustere
178 interactions were not previously detected by
two-hybrid or AP-MS techniques.
179 III where the instability is dependent upon
two hybrid-
prone sequences.
180 Using yeast
two-hybrid protein interaction studies, we found that a
181 igh-content imaging and a mammalian membrane
two-hybrid protein-protein interaction method, we identi
182 ith our interactions studies including yeast
two-hybrid,
pull-down, and in planta fluorescence resona
183 for the interacting fragments using a yeast
two-hybrid reporter system.
184 We performed a yeast
two hybrid screen with SR34 as bait and discovered SR45
185 The interaction was found in a yeast
two-hybrid screen (human leukocyte and mononuclear libra
186 Both a yeast
two-hybrid screen and a pull-down assay identified plast
187 Using a yeast
two-hybrid screen and coimmunoprecipitation assays, we s
188 C2.2]) in a yeast (Saccharomyces cerevisiae)
two-hybrid screen and have confirmed this interaction th
189 regulation, we performed a large-scale yeast
two-hybrid screen and identified CONSTANS-LIKE 3 (COL3)/
190 We performed a yeast
two-hybrid screen and identified the adaptor protein, FH
191 interacting partner of SIS8 based on a yeast
two-hybrid screen and in planta bimolecular fluorescence
192 interacting factor for Kbtbd5 using a yeast
two-hybrid screen and in vitro binding assays.
193 t with known clock components in a mammalian
two-hybrid screen and modulate in vitro cellular rhythms
194 In this study, using a yeast
two-hybrid screen approach, we identified the NF-YB and
195 Here, we conducted yeast
two-hybrid screen assay and identified an E3 ligase, COP
196 Using an unbiased yeast
two-hybrid screen for interactions between murine RNA-bi
197 Here, using a yeast
two-hybrid screen for proteins interacting with its C-te
198 A yeast
two-hybrid screen has revealed that the transcriptional
199 Here, a yeast
two-hybrid screen revealed that RABV P interacts with th
200 Using a split-ubiquitin yeast
two-hybrid screen that covers a test-space of 6.4 x 10(6
201 Using a membrane-based
two-hybrid screen to identify proteins that bind to PCDH
202 We have now performed a yeast
two-hybrid screen using dysbindin as bait against a card
203 hat may remove the CRD, we performed a yeast
two-hybrid screen using twitchin kinase as bait.
204 otein interaction partners of NBP35, a yeast-
two-hybrid screen was carried out that identified NBP35
205 Using a yeast
two-hybrid screen, we discovered an interaction between
206 Using a yeast
two-hybrid screen, we identified cyclin L2 as a DCAF1-in
207 Using a yeast
two-hybrid screen, we identified four cytoskeletal compo
208 Using a yeast
two-hybrid screen, we identified the hematopoietic-restr
209 Furthermore, using a yeast
two-hybrid screen, we identified the motor protein Kif15
210 Using a yeast
two-hybrid screen, we searched for novel AIRE-interactin
211 in was identified by a Split-Ubiquitin Yeast-
Two-Hybrid screen.
212 rotein interaction data from a focused yeast
two-hybrid screen.
213 eneurin-1 ICD interaction partner in a yeast
two-hybrid screen.
214 tify Wor1-interacting proteins using a yeast
two-hybrid screen.
215 tein-protein interactions (PPIs) using yeast
two-hybrid screening (Y2H).
216 D11) as a new interactor of PLEKHA7 by yeast
two-hybrid screening and by mass spectrometry analysis o
217 Using yeast
two-hybrid screening and co-immunoprecipitation assays,
218 Using an unbiased yeast
two-hybrid screening and complementary approaches, we fo
219 KDR interactors using a combination of yeast
two-hybrid screening and dedicated confirmations with bi
220 oteins in Vpu function, we carried out yeast
two-hybrid screening and identified a previously reporte
221 ng hetero- or homodimers, we conducted yeast-
two-hybrid screening and identified an SVP-like MADS-box
222 in Vpu's function, here we carried out yeast
two-hybrid screening and identified the V0 subunit C of
223 Using yeast
two-hybrid screening and pull-down assays, MDT-28/PLIN-1
224 Yeast
two-hybrid screening combined with bimolecular fluoresce
225 Yeast
two-hybrid screening identified an interaction between N
226 To address this, we performed yeast
two-hybrid screening of PRMT7 and identified argininosuc
227 A yeast
two-hybrid screening revealed a specific interaction wit
228 Yeast
two-hybrid screening revealed several interactive partne
229 Yeast
two-hybrid screening suggests that XB130 interacts with
230 TAF4b functions in spermatogenesis, we used
two-hybrid screening to identify a novel TAF4b-interacti
231 Here, we have used yeast-
two-hybrid screening to identify OsPIP5K1, a member of t
232 40 was found to be a centrin target by yeast-
two-hybrid screening using both Homo sapiens centrin 2 (
233 To identify the presumed receptor proteins,
two-hybrid screening was performed.
234 SPBB1 was identified through yeast
two-hybrid screening with the kinase-dead TbPLK as the b
235 proteins determined using multivector yeast
two-hybrid screening, and these PPIs were further suppor
236 Here, using yeast
two-hybrid screening, co-immunoprecipitation, and severa
237 Through yeast
two-hybrid screening, we identify the centrosomal protei
238 e interacting partner of NLRC3 through yeast
two-hybrid screening.
239 mation efficiency is critical, such as yeast
two-hybrid screening.
240 artner of the E2 protein of CSFV using yeast
two-hybrid screening.
241 of thromboxane A2 receptor (TPbeta) by yeast
two-hybrid screening.
242 ins that can interact with JSRV Env by yeast
two-hybrid screening.
243 the roles of IDRs in CBP, we performed yeast-
two-hybrid screenings of placenta and lung cancer cDNA l
244 Employing pooled RNAi and yeast
two-hybrid screenings, we report that the mitochondrial
245 aling pathway components, we performed yeast
two-hybrid screens and identified the muscle-specific pr
246 Mutational analysis, combined with bacterial
two-hybrid screens and in vivo functional assays, verifi
247 ify host targets of AVR1, we performed yeast
two-hybrid screens and selected Sec5 as a candidate.
248 Yeast-
two-hybrid screens identify RhoC as a Fam65b binding par
249 Yeast
two-hybrid screens indicated that GhDsPTP3a interacts wi
250 Here we performed yeast
two-hybrid screens of 3,305 baits against 3,606 preys (
251 Yeast
two-hybrid screens revealed that CEFIP interacts with th
252 tor-protein interactions, we conducted yeast
two-hybrid screens using the cytosolic domains of ETR1 a
253 In addition, using yeast
two-hybrid screens we identified several candidates of N
254 Using STK38 as bait in yeast-
two-hybrid screens, we discovered STK38 as a novel bindi
255 s results from electron microscopy and yeast
two-hybrid screens.
256 er NCX1 was found to interact with Ano6 in a
two-hybrid split-ubiquitin screen.
257 Cross-linking, protein capture and
two-hybrid studies demonstrated that Spc and PilA intera
258 Yeast
two-hybrid studies revealed that meiosis-expressed gene
259 contradicting bacterial two-hybrid and yeast
two-hybrid studies suggesting that either the former or
260 n interaction which we confirmed using yeast
two-hybrid studies.Taken together, we find evidence for
261 In a yeast
two-hybrid study, we identified a novel interaction betw
262 TaFROG-interacting protein based on a yeast
two-hybrid study.
263 A Bacterial
Two Hybrid system indicates that DauA and the sensor com
264 By employing a bacterial
two hybrid system, pull down assays and surface plasmon
265 is sensitivity issue, we introduced in vitro
two-hybrid system (IVT2H) into microfluidic drops and de
266 interactions naively tested using the yeast
two-hybrid system and 2.7 times better than for randomly
267 Using the yeast
two-hybrid system and bimolecular fluorescence complemen
268 were systematically mapped using a mammalian
two-hybrid system and confirmed using a co-immunoprecipi
269 ly developed interaction assays (e.g., yeast
two-hybrid system and split-ubiquitin assay) usually are
270 We here report on a genome-wide screening by
two-hybrid system for MmpL3 binding partners.
271 A bacterial
two-hybrid system screen identified bacterioferritins an
272 Here we use a yeast
two-hybrid system to identify novel TIR1 mutants with al
273 Here, using a yeast
two-hybrid system to search for AtRALF1-interacting prot
274 The BACTH-TM bacterial
two-hybrid system was successfully used to study peripla
275 temporal control of NCKX4 activity, a yeast
two-hybrid system was used to search for protein interac
276 raction of full-length PsIAA4 in vivo (yeast
two-hybrid system).
277 ecapping complex VARICOSE (VCS) in the yeast
two-hybrid system, and co-localizes with components of t
278 Using a bacterial
two-hybrid system, it could be shown that the N-terminus
279 Using a mammalian
two-hybrid system, real-time monitoring of circadian rhy
280 Using the yeast
two-hybrid system, we previously identified a swine host
281 also detected with the yeast split-ubiquitin
two-hybrid system.
282 -immunoprecipitation assay and the mammalian
two-hybrid system.
283 as a novel DAT binding partner using a yeast
two-hybrid system.
284 cription factor interactions using the yeast
two-hybrid system.
285 es NGS to remove multiple bottlenecks of the
two-hybrid system.
286 ith themselves and each other in a bacterial
two-hybrid system.
287 Two-hybrid systems can be used for investigating protein
288 g interactions involving such proteins using
two-hybrid systems has therefore been problematic.
289 eir success in mapping protein interactions,
two-hybrid systems have remained mostly untouched by imp
290 The
two-hybrid systems rely on one-versus-all methods in whi
291 c studies of protein-protein interactions by
two-hybrid techniques and of affinity-purified protein c
292 volved in PPIs by advancing the use of yeast
two-hybrid technology.
293 PIP5K6 interacted with MPK6 in yeast
two-hybrid tests, immuno-pull-down assays, and by bimole
294 cosubcellular enrichment analysis and yeast
two-hybrid validation.
295 We applied a yeast-
two-hybrid (
Y2H) analysis to screen for ubiquitin varian
296 teractions (PPIs) of HEV by systematic Yeast
two-hybrid (
Y2H) and LuMPIS screens, providing a basis f
297 We employed yeast-
two-hybrid (
Y2H) assays, co-immunoprecipitation, transcr
298 We performed a yeast
two-hybrid (
Y2H) screen and uncovered TNKS as a putative
299 We recently used yeast
two-hybrid (
Y2H) screening to identify a small set of no
300 cs to determine patterns of gene flow across
two hybrid zones formed between two independent pairs of