1 are specific for spermatogenesis between the
two hybrids.
2 haracterized their interactions by bacterial
two-hybrid analyses and could show that the permease Bce
3 lize phylogenetic conservation and bacterial
two-hybrid analyses to predict residues in Crl important
4 Yeast
two-hybrid analyses using serial domain deletion constru
5 molecular complementation assays, i.e. yeast
two-hybrid analysis and Arabidopsis leaf protoplast spli
6 s actually binds to ankyrin-G, both in yeast
two-hybrid analysis and by coimmunoprecipitation in situ
7 We have demonstrated using bacterial
two-hybrid analysis and confirmatory coelution experimen
8 nascent PG processing in vivo, and bacterial
two-hybrid analysis identified an MltG-PBP1b interaction
9 Here we use bacterial
two-hybrid analysis in vivo and p-benzoyl-phenylalanine
10 oteome, we carried out a comprehensive yeast
two-hybrid analysis of all the putative proteins encoded
11 Two-hybrid analysis revealed that the dynamins are part
12 Yeast
two-hybrid analysis reveals that SIX6OS1 interacts with
13 Yeast
two-hybrid analysis showed no evidence of a direct inter
14 Yeast
two-hybrid analysis shows that the rod domain of KRT1 in
15 Here, we used bacterial
two-hybrid analysis to identify a surface-exposed alpha-
16 We used yeast (Saccharomyces cerevisiae)
two-hybrid analysis to map the binding site of Bud23 on
17 A yeast
two-hybrid analysis uncovered the actin-depolymerizing f
18 hat disrupted the interaction, as assayed by
two-hybrid analysis, did not display a growth defect.
19 vel binding partner of E5, YIPF4 using yeast
two-hybrid analysis.
20 loss of interaction that we have defined by
two-hybrid analysis.
21 ay crystallography, electron microscopy, and
two-hybrid analysis.
22 Yeast-
two-hybrid and a green-fluorescent protein fragment comp
23 deacetylase subunits were observed in yeast
two-hybrid and bimolecular fluorescence assays, consiste
24 Yeast
two-hybrid and bimolecular fluorescence complementation
25 In yeast (Saccharomyces cerevisiae)
two-hybrid and bimolecular fluorescence complementation
26 Furthermore, yeast
two-hybrid and bimolecular fluorescence complementation
27 Yeast- or protoplast-based
two-hybrid and bimolecular fluorescent complementation a
28 Our complementary yeast
two-hybrid and biochemical assays reveal that CHD7 is a
29 Yeast
two-hybrid and biochemical studies have revealed that th
30 Results from yeast
two-hybrid and co-expression in Escherichia coli confirm
31 Two-hybrid and co-immunoprecipitation analysis has been
32 Here, using yeast
two-hybrid and co-immunoprecipitation approaches, we sho
33 Yeast
two-hybrid and co-immunoprecipitation assays demonstrate
34 Yeast
two-hybrid and coimmunoprecipitation analyses associated
35 Additional
two-hybrid and coimmunoprecipitation assays demonstrated
36 On the basis of yeast
two-hybrid and coimmunoprecipitation assays, we demonstr
37 Using both yeast
two-hybrid and copurification approaches, we identified
38 Analysis of interactions using the bacterial
two-hybrid and cross-linking assays showed that TraE and
39 Yeast
two-hybrid and direct pulldown assays revealed that the
40 Bacterial
two-hybrid and gene-reporter assays demonstrated that Fs
41 (an E3 ubiquitin ligase), as shown by yeast
two-hybrid and in vitro pulldown assays.
42 Combined yeast
two-hybrid and protein array experiments demonstrated th
43 Furthermore, yeast
two-hybrid and pull-down experiments indicated that MYC2
44 Two-hybrid and pulldown assays demonstrated that UL20, b
45 Importantly, bacterial
two-hybrid and quantitative imaging assays revealed a si
46 therian and avian cDNA libraries using yeast-
two-hybrid and split-ubiquitin systems.
47 Transcriptional assays, such as yeast
two-hybrid and TANGO, that convert transient protein-pro
48 Modeling, yeast
two-hybrid,
and functional data reveal that this PF2-lik
49 our USH proteins using colocalization, yeast
two-hybrid,
and pull-down assays.
50 coimmunoprecipitation, colocalization, yeast
two-hybrid,
and small interfering RNA (siRNA) analyses.
51 irus replication, we have been using a yeast
two-hybrid approach to identify host proteins that inter
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 3A-DCTN3 interaction identified by the yeast
two-hybrid approach was further confirmed in mammalian c
55 TolA-pIII complex, we developed a bacterial
two-hybrid approach, named Oxi-BTH, suited for studying
56 Here, using a yeast
two-hybrid approach, we have assessed interactions betwe
57 By using the Yeast
Two-Hybrid approach, we identified a disintegrin and met
58 Using a yeast
two-hybrid approach, we identified cellular protein DCTN
59 Using a yeast
two-hybrid approach, we identified the 5'-3' exonuclease
60 Using a bacterial
two-hybrid approach, we show that the three key LTA synt
61 PI maps at proteome scale, first using yeast
two-hybrid approaches and more recently via affinity pur
62 We used proteomic and yeast
two-hybrid approaches to elucidate host factors involved
63 Using bacterial
two-hybrid approaches, we showed that the P. aeruginosa
64 nity purification-mass spectrometry or yeast
two-hybrid approaches.
65 de, extended-peptide, and protein levels and
two "hybrid"
approaches (i.e., protein calibrator with S
66 By a combination of yeast-
two hybrid assay, in vitro binding, and coimmunoprecipit
67 s) in human cells, termed mammalian-membrane
two-hybrid assay (MaMTH).
68 Bacterial
two-hybrid assay and accumulation of Gp0.6 only in MreB-
69 We performed a yeast
two-hybrid assay and identified hematopoietically expres
70 interact with Hsp90Ecin vivo in a bacterial
two-hybrid assay and in vitro in a bio-layer interferome
71 e in ClpB interaction in vivo in a bacterial
two-hybrid assay and in vitro in a fluorescence anisotro
72 ns also directly interact in vivo in a yeast
two-hybrid assay and in vitro through ammonium sulfate c
73 s transcription factor prey library by yeast
two-hybrid assay and isolated six class I members of the
74 reliminary experiments involving a bacterial
two-hybrid assay are presented that corroborate the exis
75 The yeast
two-hybrid assay identified that proteasome subunit alph
76 Yeast
two-hybrid assay indicated that the PDH45 protein intera
77 Yeast
two-hybrid assay revealed that the N-terminal region of
78 Furthermore, results of the mammalian
two-hybrid assay showed that cyclin-dependent kinase 3 (
79 reened a kidney cDNA library through a yeast
two-hybrid assay using NKCC2 C terminus as bait.
80 h deletion analysis, co-immunoprecipitation,
two-hybrid assay, and pulldown assays with expressed pro
81 cessary for the interaction with FeoB in the
two-hybrid assay, and when either of these amino acids w
82 ructure was corroborated using the bacterial
two-hybrid assay, biochemical characterization of the pu
83 ions with core exocyst subunits in the yeast
two-hybrid assay, cytoplasmic localization, and genetic
84 According to a yeast
two-hybrid assay, ORRM1 interacts selectively with penta
85 We searched for such proteins by yeast
two-hybrid assay, using GARP as a bait to screen a human
86 Using a modified version of the mammalian
two-hybrid assay, we demonstrate that the interaction st
87 Using the above-mentioned
two-hybrid assay, we found that zebrafish Tmc1 and Tmc2a
88 racting proteins were screened using a yeast
two-hybrid assay.
89 at prevent DEPTOR binding to mTOR in a yeast-
two-hybrid assay.
90 proteins were identified by a modified yeast
two-hybrid assay.
91 high-throughput, array-based, directed yeast
two-hybrid assay.
92 ing proteins with GLP-1R by a membrane yeast
two-hybrid assay.
93 was further confirmed by Co-IP and mammalian
two-hybrid assay.
94 ck proteins, Hsp16.9 and Hsp17.5, in a yeast
two-hybrid assay.
95 amK and the two proteins interact in a yeast
two-hybrid assay.
96 -interacting proteins using a modified yeast
two-hybrid assay.
97 modulate its function, we performed a yeast
two-hybrid assay.
98 subunits including Sgf29 and Spt7 in a yeast
two-hybrid assay.
99 PYL6 and MYC2 interact in yeast
two hybrid assays and the interaction is enhanced in the
100 Site-directed mutagenesis and yeast-
two hybrid assays identified DnaA and DnaN binding sites
101 In yeast-
two hybrid assays, ORRM3 interacts with RIP1, ORRM2 and
102 ters, subcellular localization and bacterial
two hybrid assays.
103 length protein in vivo, as measured by yeast-
two hybrid assays.
104 e ESCRT-III-related proteins CHMP1A in yeast
two hybrid assays.
105 ABD1 directly interacts with ABI5 in yeast
two-hybrid assays and associates with ABI5 in vivo by co
106 By yeast-
two-hybrid assays and chromatin immunoprecipitation we d
107 Yeast
two-hybrid assays and coimmunoprecipitation experiments
108 and TMC1 or TMC2 was observed in both yeast
two-hybrid assays and coimmunoprecipitation experiments.
109 o the blue-light photoreceptor FKF1 in yeast
two-hybrid assays and delays flowering in Arabidopsis wh
110 with beta-catenin was confirmed using yeast
two-hybrid assays and in vitro synthesized proteins.
111 fects in vivo, ARC3 interacted with FtsZ2 in
two-hybrid assays and inhibited FtsZ2 assembly in a hete
112 Yeast
two-hybrid assays established a direct interaction of Ce
113 cular fluorescence complementation and yeast-
two-hybrid assays indicated that the IDR3 domain does no
114 Furthermore, our yeast
two-hybrid assays show that MoVps17 and MoVps5 can inter
115 -seq and proteomics data together with yeast
two-hybrid assays suggest that MS23 along with MS32, bHL
116 ass spectrometry, split-luciferase and yeast-
two-hybrid assays to generate a single reliability score
117 we used membrane-based split ubiquitin yeast
two-hybrid assays to identify novel GLP1R interactors in
118 Here, we carry out directional yeast
two-hybrid assays to identify the interactions between t
119 tion of pull-downs, mass spectrometry, yeast
two-hybrid assays, and chemical genomics, we demonstrate
120 Based on bacterial
two-hybrid assays, CelR homodimerizes but does not inter
121 In yeast
two-hybrid assays, FgMcm1 interacted with Mat1-1-1 and F
122 with P. blakesleeanus Ras homologs in yeast
two-hybrid assays, indicating that MadC is a regulator o
123 amily member periplakin, identified in yeast
two-hybrid assays, interacted with a membrane-proximal d
124 In yeast
two-hybrid assays, MAS2 interacted with splicing and rib
125 fatty acid synthase II (FAS-II) in bacterial
two-hybrid assays, suggesting essentiality may be linked
126 Using yeast
two-hybrid assays, we determined the interactions among
127 und state failed to bind to AvrL567 in yeast
two-hybrid assays, while binding was detected to the sig
128 an interact with both TTI1 and TTI2 in yeast
two-hybrid assays.
129 ptide aptamers for further analysis in yeast
two-hybrid assays.
130 with UNC-116 kinesin-1 heavy chain in yeast
two-hybrid assays.
131 h the CAR ligand-binding domain in mammalian
two-hybrid assays; and 5) disrupts CAR binding to the pr
132 In this study,
two hybrid biochemical routes combining lignin chemical
133 Using yeast
two-hybrid,
biochemical, and cellular assays, we determi
134 Conversely, protein-level and the
two hybrid calibrations achieved good quantitative accur
135 offspring phenotypes suggest the presence of
two hybrid classes, F1s and var. incana backcrosses, as
136 Yeast
two-hybrid,
co-immunoprecipitation and pulldown experime
137 binding partner of IL-13Ralpha2 using yeast
two-hybrid,
co-immunoprecipitation, co-localization and
138 Yeast
two-hybrid,
coimmunoprecipitation and bimolecular fluore
139 size exclusion chromatography, and bacterial
two-hybrid data revealed that PilM forms dimers mediated
140 Furthermore, yeast
two-hybrid data showed that CPTL2 and CPT3 interact.
141 Bacterial
two-hybrid data suggested the connectivity of the cytopl
142 Competitive yeast-
two hybrid experiments indicate that the LIM domains and
143 xperiments, chemical crosslinking, bacterial
two-hybrid experiments and nuclear magnetic resonance ch
144 Yeast
two-hybrid experiments confirmed the direct interaction
145 Two-hybrid experiments demonstrate self-interaction of t
146 Yeast
two-hybrid experiments identified PG core proteins ABC1K
147 Yeast
two-hybrid experiments indicate that the interaction of
148 Yeast
two-hybrid experiments suggested that the phosphorylatio
149 and IAA7 in yeast (Saccharomyces cerevisiae)
two-hybrid experiments, indicating that these proteins w
150 tory subunits of PP2A, Wdb and Wrd, in yeast
two-hybrid experiments.
151 Two hybrid fluorinated double-chain surfactants with a d
152 Using a yeast
two-hybrid genome-wide screen, we identified novel inter
153 pha-helix(656-666), which are required for a
two-hybrid Gln3-Tor1 interaction, also abolished rapamyc
154 Using yeast
two-hybrid,
GST pull-down, co-immunoprecipitation and bi
155 ary methods-a high-throughput enhanced yeast
two-hybrid (
HT-eY2H) assay and a mammalian-cell-based Ga
156 s between the various MORF proteins by yeast
two-hybrid,
in vitro pulldown, and bimolecular fluoresce
157 Two-hybrid interaction experiments suggest that the inte
158 to its principal endomembrane cargo, a yeast
two-hybrid library of Arabidopsis thaliana cDNAs was scr
159 Using a yeast (Saccharomyces cerevisiae)
two-hybrid library of S. reilianum-infected maize tissue
160 Screening a yeast
two-hybrid library revealed that UNC-89 interacts with p
161 as a Myb1-binding protein using a bacterial
two-hybrid library screening system.
162 Using bacterial
two-hybrid library screening, NR1D1 was identified as a
163 Here, we screened a yeast
two-hybrid library using the Arabidopsis LDAP3 isoform a
164 We screened a yeast
two-hybrid library using the central domain of ubiquilin
165 Therefore, a pancreatic islet yeast
two-hybrid library was produced and searched for glucoki
166 Using an RXR-VDR mammalian
two-hybrid (
M2H) biologic assay system, we measured vita
167 Recently, we constructed a yeast
two-hybrid map around three rice proteins that control t
168 cadherin 23 with expressed exon 68) by yeast
two-hybrid mating and co-transformation protocols, pulld
169 we utilized the bacterial adenylate cyclase
two-hybrid method and carried out a saturation mutagenes
170 rall prediction accuracy, with the in-silico
two-hybrid method contributing most to performance.
171 we used random mutagenesis and the mammalian
two-hybrid method MAPPIT (mammalian protein-protein inte
172 re, we present a massively multiplexed yeast
two-hybrid method, CrY2H-seq, which uses a Cre recombina
173 Here, we demonstrate by yeast
two-hybrid method, immunoprecipitation assays, and surfa
174 Using yeast
two-hybrid methods, we identified a large set of protein
175 sequence-based prediction methods: in-silico
two-hybrid,
mirror-tree, gene fusion, phylogenetic profi
176 Sho1p PPIs through the use of membrane yeast
two-hybrid (
MYTH), an assay specifically suited to ident
177 The volatile profile of
two hybrids of "Radicchio di Chioggia", Corelli and Bott
178 es associated with ontologic cancer sets and
two hybrids of separate experimental replicates clustere
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 ture (SILAC) data with high-throughput yeast
two hybrid results, we showed that five of these protein
184 in Containing Protein, HvELMOD_C, in a yeast
two hybrid screen for proteins interacting with HvMAGAP1
185 We performed a yeast
two hybrid screen with SR34 as bait and discovered SR45
186 C2.2]) in a yeast (Saccharomyces cerevisiae)
two-hybrid screen and have confirmed this interaction th
187 regulation, we performed a large-scale yeast
two-hybrid screen and identified CONSTANS-LIKE 3 (COL3)/
188 We performed a yeast
two-hybrid screen and identified the adaptor protein, FH
189 interacting partner of SIS8 based on a yeast
two-hybrid screen and in planta bimolecular fluorescence
190 interacting factor for Kbtbd5 using a yeast
two-hybrid screen and in vitro binding assays.
191 t with known clock components in a mammalian
two-hybrid screen and modulate in vitro cellular rhythms
192 In this study, using a yeast
two-hybrid screen approach, we identified the NF-YB and
193 On the basis of a yeast
two-hybrid screen for the MT1-MMP cytoplasmic tail-bindi
194 A yeast
two-hybrid screen has identified the adaptor protein X11
195 A yeast
two-hybrid screen has revealed that the transcriptional
196 A bacterial
two-hybrid screen identified an interaction between CtsP
197 Here, a yeast
two-hybrid screen revealed that RABV P interacts with th
198 Using a split-ubiquitin yeast
two-hybrid screen that covers a test-space of 6.4 x 10(6
199 -terminal subdomain that was used in a yeast
two-hybrid screen that identified the proline-rich domai
200 We have previously shown through a yeast
two-hybrid screen that it is also a cardiac binding part
201 nding of MTM1 function, we conducted a yeast
two-hybrid screen to identify MTM1-interacting proteins.
202 otes genomic stability by performing a yeast
two-hybrid screen to identify potential substrates/inter
203 Using a membrane-based
two-hybrid screen to identify proteins that bind to PCDH
204 cular functions of FTO, we performed a yeast
two-hybrid screen to identify the protein(s) that could
205 TDP-43 protein interactors found in a yeast
two-hybrid screen using an adult human brain cDNA librar
206 teractions, we performed a large-scale yeast
two-hybrid screen using both wild-type (WT) and six diff
207 We have now performed a yeast
two-hybrid screen using dysbindin as bait against a card
208 hat may remove the CRD, we performed a yeast
two-hybrid screen using twitchin kinase as bait.
209 otein interaction partners of NBP35, a yeast-
two-hybrid screen was carried out that identified NBP35
210 luence its subcellular localization, a yeast
two-hybrid screen was performed.
211 A yeast-
two-hybrid screen with CPRabA5e as bait revealed 13 inte
212 Using a yeast
two-hybrid screen, we discovered an interaction between
213 Using a yeast
two-hybrid screen, we identified a novel transcription c
214 Using a yeast
two-hybrid screen, we identified cyclin L2 as a DCAF1-in
215 Using a yeast
two-hybrid screen, we identified four cytoskeletal compo
216 Using a yeast
two-hybrid screen, we identified the anti-apoptotic prot
217 Using a yeast
two-hybrid screen, we identified the hematopoietic-restr
218 Furthermore, using a yeast
two-hybrid screen, we identified the motor protein Kif15
219 Using a yeast
two-hybrid screen, we searched for novel AIRE-interactin
220 eneurin-1 ICD interaction partner in a yeast
two-hybrid screen.
221 tify Wor1-interacting proteins using a yeast
two-hybrid screen.
222 we performed a comprehensive pairwise yeast
two-hybrid screen.
223 in was identified by a Split-Ubiquitin Yeast-
Two-Hybrid screen.
224 rotein interaction data from a focused yeast
two-hybrid screen.
225 genase in a yeast (Saccharomyces cerevisiae)
two-hybrid screen; other TX and TN proteins interacted w
226 tein-protein interactions (PPIs) using yeast
two-hybrid screening (Y2H).
227 D11) as a new interactor of PLEKHA7 by yeast
two-hybrid screening and by mass spectrometry analysis o
228 Using yeast
two-hybrid screening and co-immunoprecipitation assays,
229 oteins in Vpu function, we carried out yeast
two-hybrid screening and identified a previously reporte
230 Yeast
two-hybrid screening combined with bimolecular fluoresce
231 Using yeast
two-hybrid screening coupled with a candidate approach,
232 We isolated Myosin Vc in a yeast
two-hybrid screening for proteins that interact with Rab
233 Yeast
two-hybrid screening identified an interaction between N
234 To address this, we performed yeast
two-hybrid screening of PRMT7 and identified argininosuc
235 A yeast
two-hybrid screening revealed a specific interaction wit
236 Yeast
two-hybrid screening suggests that XB130 interacts with
237 40 was found to be a centrin target by yeast-
two-hybrid screening using both Homo sapiens centrin 2 (
238 In a
two-hybrid screening using the catalytic Sec7 domain as
239 To identify the presumed receptor proteins,
two-hybrid screening was performed.
240 SPBB1 was identified through yeast
two-hybrid screening with the kinase-dead TbPLK as the b
241 proteins determined using multivector yeast
two-hybrid screening, and these PPIs were further suppor
242 By means of yeast (Saccharomyces cerevisiae)
two-hybrid screening, we identified basic helix-loop-hel
243 Through yeast
two-hybrid screening, we identified tumor suppressor p27
244 Through yeast
two-hybrid screening, we identify the centrosomal protei
245 ins that can interact with JSRV Env by yeast
two-hybrid screening.
246 entified by yeast (Saccharomyces cerevisiae)
two-hybrid screening.
247 rotein 1 (SR1IP1) was identified by CytoTrap
two-hybrid screening.
248 ified as a Vav3 interacting protein by yeast
two-hybrid screening.
249 e interacting partner of NLRC3 through yeast
two-hybrid screening.
250 mation efficiency is critical, such as yeast
two-hybrid screening.
251 artner of the E2 protein of CSFV using yeast
two-hybrid screening.
252 of thromboxane A2 receptor (TPbeta) by yeast
two-hybrid screening.
253 the roles of IDRs in CBP, we performed yeast-
two-hybrid screenings of placenta and lung cancer cDNA l
254 Employing pooled RNAi and yeast
two-hybrid screenings, we report that the mitochondrial
255 aling pathway components, we performed yeast
two-hybrid screens and identified the muscle-specific pr
256 ify host targets of AVR1, we performed yeast
two-hybrid screens and selected Sec5 as a candidate.
257 Yeast-
two-hybrid screens identify RhoC as a Fam65b binding par
258 Here we performed yeast
two-hybrid screens of 3,305 baits against 3,606 preys (
259 Yeast
two-hybrid screens revealed that CEFIP interacts with th
260 olycystic kidney disease, we performed yeast
two-hybrid screens using the C-terminus of polycystin-1
261 tor-protein interactions, we conducted yeast
two-hybrid screens using the cytosolic domains of ETR1 a
262 In addition, using yeast
two-hybrid screens we identified several candidates of N
263 argets in the host cells, we performed yeast
two-hybrid screens, allowing us to find 48 high-confiden
264 Using STK38 as bait in yeast-
two-hybrid screens, we discovered STK38 as a novel bindi
265 s results from electron microscopy and yeast
two-hybrid screens.
266 er NCX1 was found to interact with Ano6 in a
two-hybrid split-ubiquitin screen.
267 Yeast
two-hybrid studies revealed that meiosis-expressed gene
268 n interaction which we confirmed using yeast
two-hybrid studies.Taken together, we find evidence for
269 In a yeast
two-hybrid study, we identified a novel interaction betw
270 TaFROG-interacting protein based on a yeast
two-hybrid study.
271 A Bacterial
Two Hybrid system indicates that DauA and the sensor com
272 By employing a bacterial
two hybrid system, pull down assays and surface plasmon
273 is sensitivity issue, we introduced in vitro
two-hybrid system (IVT2H) into microfluidic drops and de
274 r-binding protein PspF to create an in vitro
two-hybrid system (IVT2H), capable of carrying out gene
275 Using the yeast
two-hybrid system and bimolecular fluorescence complemen
276 were systematically mapped using a mammalian
two-hybrid system and confirmed using a co-immunoprecipi
277 ly developed interaction assays (e.g., yeast
two-hybrid system and split-ubiquitin assay) usually are
278 brane-based yeast (Saccharomyces cerevisiae)
two-hybrid system established that tetraspanins can phys
279 its original description in 1989, the yeast
two-hybrid system has been extensively used to identify
280 domains of each immune receptor in the yeast
two-hybrid system in a kinase activity-dependent manner.
281 criptional effectors (LITEs), an optogenetic
two-hybrid system integrating the customizable TALE DNA-
282 d the Sos recruitment system, an alternative
two-hybrid system method to detect protein-protein inter
283 A bacterial
two-hybrid system screen identified bacterioferritins an
284 Here we use a yeast
two-hybrid system to identify novel TIR1 mutants with al
285 we used the yeast (Saccharomyces cerevisiae)
two-hybrid system to screen for NF-YC1-interacting prote
286 Here, using a yeast
two-hybrid system to search for AtRALF1-interacting prot
287 raction of full-length PsIAA4 in vivo (yeast
two-hybrid system).
288 Using a bacterial
two-hybrid system, it could be shown that the N-terminus
289 y-capture complex purification and the yeast
two-hybrid system, may produce inaccurate data sets owin
290 Using a modified yeast substrate trapping
two-hybrid system, we identified a cytosolic adaptor pro
291 as a novel DAT binding partner using a yeast
two-hybrid system.
292 aptured proteins was verified in a bacterial
two-hybrid system.
293 also detected with the yeast split-ubiquitin
two-hybrid system.
294 -immunoprecipitation assay and the mammalian
two-hybrid system.
295 PIP5K6 interacted with MPK6 in yeast
two-hybrid tests, immuno-pull-down assays, and by bimole
296 f the NS4A TM domain in a well-characterized
two-hybrid TM protein interaction system.
297 teractions (PPIs) of HEV by systematic Yeast
two-hybrid (
Y2H) and LuMPIS screens, providing a basis f
298 ystems, such as affinity purification, yeast
two-hybrid (
Y2H) and protein-fragment complementation as
299 We performed a yeast
two-hybrid (
Y2H) screen and uncovered TNKS as a putative
300 We recently used yeast
two-hybrid (
Y2H) screening to identify a small set of no