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1 ation (electron microscopy) and interaction (coimmunoprecipitation).
2 binding sites and can interact with EBNA2 by coimmunoprecipitation.
3  a combination of covalent cross-linking and coimmunoprecipitation.
4 s not interact with Yap1, as demonstrated by coimmunoprecipitation.
5 cence, in situ proximity ligation assay, and coimmunoprecipitation.
6 ween chIL-17RA and chIL-17A was confirmed by coimmunoprecipitation.
7 ed membrane protein 7 (VAMP7) is detected by coimmunoprecipitation.
8  between otoferlin and AP-2 was confirmed by coimmunoprecipitation.
9      Homomultimer formation was confirmed by coimmunoprecipitation.
10  cross-linking, followed by Western blot and coimmunoprecipitation.
11 UALIZED ENDOCYTIC TRAFFICKING DEFECTIVE1) by coimmunoprecipitation.
12 inase B and p38 upstream kinases as shown by coimmunoprecipitation.
13 racts with Rga7 in affinity purification and coimmunoprecipitation.
14 NaC and HDAC7 form a complex, as detected by coimmunoprecipitation.
15  by bioinformatics, immunocytochemistry, and coimmunoprecipitation.
16 tern blotting (WB), immunocytochemistry, and coimmunoprecipitation.
17 he interacting regions have relied mainly on coimmunoprecipitation, a technique with some pitfalls.
18 s stably expressing LANA and was verified by coimmunoprecipitation analyses and with purified protein
19                         Yeast two-hybrid and coimmunoprecipitation analyses associated ANKRD1 with nu
20 Forster resonance energy transfer (FRET) and coimmunoprecipitation analyses demonstrated that Gag and
21 vo photocross-linking along with genetic and coimmunoprecipitation analyses dissecting interactions b
22  by >30-fold), subcellular distribution, and coimmunoprecipitation analyses lead us to propose that V
23 escence resonance energy transfer (FRET) and coimmunoprecipitation analyses, we observed increased in
24                                              Coimmunoprecipitation analysis and proximity ligation as
25 nit of integrin alpha2beta1 to platelets and coimmunoprecipitation analysis confirmed integrin alpha2
26  Moreover, an unbiased proteomics screen and coimmunoprecipitation analysis identified Galphas as a n
27                                              Coimmunoprecipitation analysis of cholesterol-loaded cel
28                                              Coimmunoprecipitation analysis revealed the physical int
29                                              Coimmunoprecipitation analysis reveals for the first tim
30                                  Finally, by coimmunoprecipitation analysis, we found that ASF1 physi
31 Rab31 was found to interact with the EGFR by coimmunoprecipitation and affinity pulldown analyses, an
32 ntain only the miRNA 3' box was confirmed by coimmunoprecipitation and an in situ proximity ligation
33 d in planta, we further demonstrated by both coimmunoprecipitation and bimolecular fluorescence compl
34           SlCipk6 and SlRd2 interacted using coimmunoprecipitation and bimolecular fluorescence compl
35                                 We conducted coimmunoprecipitation and bimolecular fluorescence compl
36                            Yeast two-hybrid, coimmunoprecipitation and bimolecular fluorescent comple
37                                              Coimmunoprecipitation and bioluminescence resonance ener
38  the A2A receptor and SAP102 was verified by coimmunoprecipitation and by tracking its impact on rece
39 or-Galphai-GPR complex was also confirmed by coimmunoprecipitation and cell fractionation.
40 tion between RRP1B and SRSF1 was verified by coimmunoprecipitation and coimmunofluorescence.
41  and have confirmed this interaction through coimmunoprecipitation and colocalization assays in the C
42 en these two proteins was confirmed by their coimmunoprecipitation and colocalization in cultured cel
43 teraction was confirmed in infected cells by coimmunoprecipitation and colocalization of FAK with P i
44 STAT3 and FLAG-tagged STAT3 and showed using coimmunoprecipitation and colocalization studies that S3
45 B, the p.Gly131Glu mutant VPS33B had reduced coimmunoprecipitation and colocalization with Rab11a and
46 ia ni KLC and kinesin-1 heavy chain (KHC) by coimmunoprecipitation and colocalization.
47      We approach the protein interactions by coimmunoprecipitation and confocal microscopy and show t
48 raction of OGT and EZH2/PRC2 was detected by coimmunoprecipitation and cosedimentation experiments.
49 (phox) interacts with cytosolic cortactin by coimmunoprecipitation and double immunofluorescence stai
50 satRNA was confirmed in vivo and in vitro by coimmunoprecipitation and electrophoretic mobility shift
51                                   Using both coimmunoprecipitation and flow-cytometric strategies, we
52 hat BAK1 interacts with the BRL1 receptor by coimmunoprecipitation and fluorescence microscopy analys
53                                        Using coimmunoprecipitation and fluorescence resonance energy
54                                              Coimmunoprecipitation and glutathione S-transferase (GST
55                                              Coimmunoprecipitation and immunofluorescence analysis di
56 imentin interaction was further confirmed by coimmunoprecipitation and immunofluorescence staining to
57                                              Coimmunoprecipitation and immunofluorescence studies rev
58 with NKA-alpha2s in astrocytes, as gauged by coimmunoprecipitation and in situ proximity ligation ass
59  B-Raf(V600E) or K-Ras(G12C/D) Intriguingly, coimmunoprecipitation and in vitro binding assays reveal
60                                          RNA coimmunoprecipitation and in vitro binding studies revea
61 alidated the mLANA-Hsc70 interaction through coimmunoprecipitation and in vitro glutathione S-transfe
62                                              Coimmunoprecipitation and in vitro kinase assays demonst
63                                              Coimmunoprecipitation and in vitro pulldown assays revea
64                                              Coimmunoprecipitation and inhibition studies demonstrate
65                                              Coimmunoprecipitation and kinetic analysis showed that E
66                                        Using coimmunoprecipitation and live-cell imaging, we show tha
67                                              Coimmunoprecipitation and mass spectrometric analysis of
68 20 with dentin sialoprotein was confirmed by coimmunoprecipitation and mass spectrometry analysis of
69                                              Coimmunoprecipitation and mass spectrometry analysis rev
70                                              Coimmunoprecipitation and mass spectrometry confirmed th
71 f CESA redundancy in a mutant background, by coimmunoprecipitation and mass spectrometry using label-
72                                        Using coimmunoprecipitation and mass spectrometry, we identifi
73 croscopy and its biochemical interactions by coimmunoprecipitation and mass spectrometry.
74                                        Using coimmunoprecipitation and MS, we found the cGMP-AMP synt
75 rgo complexes associated with synapsin using coimmunoprecipitation and multidimensional protein ident
76                                              Coimmunoprecipitation and overlay experiments show that
77                                     Finally, coimmunoprecipitation and proximity ligation assays indi
78                                           By coimmunoprecipitation and pull-down assays, we provide e
79                                       Tandem coimmunoprecipitation and re-ChIP experiments with epith
80              We validated the interaction by coimmunoprecipitation and showed direct binding between
81 ternary complex of BNRF1-Daxx-H3.3-H4, using coimmunoprecipitation and size-exclusion chromatography
82 ring infection as demonstrated by reciprocal coimmunoprecipitation and supported by immunofluorescenc
83                                        Using coimmunoprecipitation and surface plasmon resonance (SPR
84 eracted with oligomeric Abeta42, as shown by coimmunoprecipitation and surface plasmon resonance/Biac
85 mouse primary hepatocytes, and mouse livers, coimmunoprecipitation and two-dimensional gel electropho
86 /INPP5F interaction could be demonstrated by coimmunoprecipitation and was potentiated by Rab5, whose
87 Protein-protein interactions were studied by coimmunoprecipitations and a systems biology approach.
88  a putative candidate and through reciprocal coimmunoprecipitations and immunocytochemistry analyses
89  binding assays, real-time quantitative PCR, coimmunoprecipitation, and ELISA techniques.
90                            Yeast two-hybrid, coimmunoprecipitation, and fluorescence resonance energy
91 by using flow cytometry, immunofluorescence, coimmunoprecipitation, and gene expression analysis.
92 irmed by glutathione S-transferase pulldown, coimmunoprecipitation, and laser confocal microscopy ass
93 n, bimolecular fluorescence complementation, coimmunoprecipitation, and mass spectrometry analyses su
94 n, bimolecular fluorescence complementation, coimmunoprecipitation, and mass spectrometry analyses su
95 d assays and associates with ABI5 in vivo by coimmunoprecipitation, and the interaction was found in
96  immunoprecipitation assay, gel-shift assay, coimmunoprecipitation, and western blottings.
97 tion, Forster resonance energy transfer, and coimmunoprecipitation approaches revealed that SERK1 int
98 h interactive regions have relied heavily on coimmunoprecipitation approaches, whose limitations incl
99                                            A coimmunoprecipitation assay followed by mass spectrometr
100                                        Using coimmunoprecipitation assay, we showed that BAM1 is capa
101 ed with the EBV immediate early R protein in coimmunoprecipitation assays and partially colocalized w
102 PIs were further supported by the results of coimmunoprecipitation assays and protein structural mode
103                       Proximity ligation and coimmunoprecipitation assays confirmed thrombin-dependen
104                                           In coimmunoprecipitation assays copper binding promotes APP
105 ith fluorescent cellular protein markers and coimmunoprecipitation assays demonstrated that FHV repli
106                    Additional two-hybrid and coimmunoprecipitation assays demonstrated that metformin
107                                 Furthermore, coimmunoprecipitation assays demonstrated that the two p
108                      Furthermore, reciprocal coimmunoprecipitation assays revealed an association bet
109                         In situ and in vitro coimmunoprecipitation assays revealed that SH2D4A direct
110                                              Coimmunoprecipitation assays revealed the presence and i
111 more, in silico analysis in combination with coimmunoprecipitation assays show an interaction between
112                                              Coimmunoprecipitation assays show that TGD5 physically i
113                                              Coimmunoprecipitation assays showed an interaction betwe
114                                              Coimmunoprecipitation assays showed lack of association
115                                              Coimmunoprecipitation assays showed that both Hdac7-u an
116                                    Moreover, coimmunoprecipitation assays showed that phosphorylation
117 bimolecular fluorescence complementation and coimmunoprecipitation assays showed that PYL4-CAR1 as we
118 abidopsis tgd1-1 Coevolutionary analysis and coimmunoprecipitation assays showed that the TGD1 L45 lo
119                                              Coimmunoprecipitation assays were used to examine the in
120  EKLF and PIAS proteins confirmed by in vivo coimmunoprecipitation assays with both exogenous and end
121                            Moreover, in vivo coimmunoprecipitation assays with tagged Mex67 document
122 ction between HSP90 and Tax was validated by coimmunoprecipitation assays, and colocalization between
123  SIVmac239 binding to CD4 in Biacore assays, coimmunoprecipitation assays, and enzyme-linked immunoso
124 3I11) interacted with TRP32 as determined by coimmunoprecipitation assays, colocalization with TRP32
125         On the basis of yeast two-hybrid and coimmunoprecipitation assays, we demonstrate here that N
126      By using mass spectrometry analysis and coimmunoprecipitation assays, we show here that VP35 is
127 n was confirmed by both peptide pulldown and coimmunoprecipitation assays, which also demonstrated th
128 Env and Zfp111 was confirmed through in vivo coimmunoprecipitation assays.
129 bimolecular fluorescence complementation and coimmunoprecipitation assays.
130 tide was sufficient for M protein binding in coimmunoprecipitation assays.
131 xes that are stable enough to be captured in coimmunoprecipitation assays.
132                                           By coimmunoprecipitation, BET proteins were found to be com
133                 Our data clearly showed that coimmunoprecipitation between AtMC1 and AtSerpin1 and fo
134           Acute beta-AR activation increases coimmunoprecipitation between P-RyR and cardiac spliced
135 omplementary inactive AR mutants and promote coimmunoprecipitation between unlike forms of AR suggest
136                                     Two-step coimmunoprecipitation (co-IP) and fluorescence resonance
137 unctions, we used two complementary methods, coimmunoprecipitation (co-IP) and proximity biotinylatio
138 , we developed in vivo beta-importin complex coimmunoprecipitation (co-IP) assays using budding yeast
139               Mass spectrometry analysis and coimmunoprecipitation (co-IP) identified a direct intera
140 hromatin immunoprecipitation (ChIP), protein coimmunoprecipitation (Co-IP), and bimolecular fluoresce
141                                Studies using coimmunoprecipitation (co-IP), bimolecular fluorescence
142 experimental and computational methods for a coimmunoprecipitation (Co-IP)-based workflow from sample
143                                              Coimmunoprecipitation, coimmunolocalization, and ChIP an
144                                              Coimmunoprecipitation (coIP) and anisotropy-based FRET (
145  of lepidopteran microtubule transport using coimmunoprecipitation, colocalization, yeast two-hybrid,
146                                              Coimmunoprecipitation confirmed a physical interaction b
147                                              Coimmunoprecipitation confirmed that AGAP1 and AGAP2 can
148                                              Coimmunoprecipitation confirmed the identified interacti
149                                              Coimmunoprecipitation confirmed the interaction between
150                                              Coimmunoprecipitation confirmed the interaction of RhgH
151 at AVR1 and Sec5 are in close proximity, and coimmunoprecipitation confirmed the interaction.
152                                              Coimmunoprecipitation demonstrated protein-protein inter
153                                              Coimmunoprecipitation demonstrated that XB130 and Tks5 i
154                                              Coimmunoprecipitation detected binding of phosphorylated
155                                            A coimmunoprecipitation experiment reveals that PPM1G bind
156  brain and formed a complex in vivo based on coimmunoprecipitation experiments and coimmunostaining i
157                                           By coimmunoprecipitation experiments and mass spectrometry,
158                                              Coimmunoprecipitation experiments and proximity ligation
159                  Yeast two-hybrid assays and coimmunoprecipitation experiments confirm the structural
160                                              Coimmunoprecipitation experiments confirmed interaction
161    Immunoprecipitation/mass spectrometry and coimmunoprecipitation experiments confirmed that PLD4 bi
162                                              Coimmunoprecipitation experiments demonstrated loss of p
163                                              Coimmunoprecipitation experiments demonstrated that RBPG
164                                              Coimmunoprecipitation experiments demonstrated that thes
165                                              Coimmunoprecipitation experiments examined protein inter
166                                    Moreover, coimmunoprecipitation experiments from rat DRG lysates i
167                                              Coimmunoprecipitation experiments further revealed that
168                                Proteomic and coimmunoprecipitation experiments identified pontin as a
169            This interaction was confirmed by coimmunoprecipitation experiments in both neuronal and n
170                                              Coimmunoprecipitation experiments in HEK293 cells reveal
171                                              Coimmunoprecipitation experiments in these tomato plants
172                                              Coimmunoprecipitation experiments indicate that two-thir
173                                              Coimmunoprecipitation experiments indicated that 5LO-CLP
174                                              Coimmunoprecipitation experiments indicated that AMPK le
175 r gH/UL116 complex formation was obtained by coimmunoprecipitation experiments on both transfected an
176 , electrophoretic mobility shift assays, and coimmunoprecipitation experiments reveal a specific inte
177 bioinformatics analyses, sequential ChIP and coimmunoprecipitation experiments reveal that Atro inter
178                                              Coimmunoprecipitation experiments revealed an interactio
179                          IL13Ralpha2-FAM120A coimmunoprecipitation experiments revealed further signa
180 N-glycosylation inhibitor tunicamycine while coimmunoprecipitation experiments revealed galectin-3 bi
181                                              Coimmunoprecipitation experiments revealed that both gK
182                                              Coimmunoprecipitation experiments revealed that core doe
183                                              Coimmunoprecipitation experiments revealed that the majo
184 imolecular fluorescence complementation, and coimmunoprecipitation experiments show that DRB3 acts do
185                                              Coimmunoprecipitation experiments showed that BMAA treat
186                                              Coimmunoprecipitation experiments showed that Hsp90 inte
187                                              Coimmunoprecipitation experiments showed that syntaxin-1
188                                              Coimmunoprecipitation experiments showed that TnBVANK1 b
189                                              Coimmunoprecipitation experiments suggest that Cu is imp
190                                              Coimmunoprecipitation experiments suggested that endogen
191 hmwBP complex was corroborated by reciprocal coimmunoprecipitation experiments using antipeptide anti
192 n SH3 binding domain, immunofluorescence and coimmunoprecipitation experiments were conducted and rev
193                                              Coimmunoprecipitation experiments were used to demonstra
194 7 (aa 693 to 982) was identified by fragment coimmunoprecipitation experiments, and a head-to-tail se
195 romoter reporter and in vitro kinase assays, coimmunoprecipitation experiments, and confocal microsco
196   A time course study of import, followed by coimmunoprecipitation experiments, confirmed that Hsp93
197 RP mutants, FRP:OCP docking simulations, and coimmunoprecipitation experiments, we conclude that the
198 nd endogenous M3R interacted with PLCbeta in coimmunoprecipitation experiments.
199 observed in both yeast two-hybrid assays and coimmunoprecipitation experiments.
200 kA N-terminal deletion mutants and performed coimmunoprecipitation experiments.
201 ble subunit alpha-2 using colocalization and coimmunoprecipitation experiments.
202      The Tcl1-Hsp70 complex was validated by coimmunoprecipitation experiments.
203 a(2) integrin-mediated adhesion, as shown by coimmunoprecipitation experiments.
204 down, in vitro ubiquitination, and in planta coimmunoprecipitation experiments.
205  in chloroplast protein homeostasis based on coimmunoprecipitation experiments.
206                                      Yet, by coimmunoprecipitation, fluorescence microscopy, and a pr
207 ssociation of these proteins is evident from coimmunoprecipitation followed by mass spectrometry, coe
208 lathrin adaptor proteins AP2-mu2 revealed by coimmunoprecipitation, followed by a decrease in associa
209 east-two hybrid assay, in vitro binding, and coimmunoprecipitation from mouse spermatocytes, we ident
210        Moreover, MRTF-A and YAP associate in coimmunoprecipitations from S1P-stimulated cells.
211                                              Coimmunoprecipitation-immunoblot analyses in the presenc
212                                              Coimmunoprecipitation, immunofluorescent, and electrophy
213                                              Coimmunoprecipitation, immunohistochemistry, confocal im
214  for Nm23-H1, verifying their interaction by coimmunoprecipitation in 4T1 cells as well as in human M
215 ed protein 97 (SAP97; also known as DLG1) by coimmunoprecipitation in human embryonic 293 (HEK 293) c
216 -G, both in yeast two-hybrid analysis and by coimmunoprecipitation in situ in HEK293 cells expressing
217 ership of UGT1A_i2 and PKM2 was confirmed by coimmunoprecipitation in the HT115 colon cancer cells an
218                              As indicated by coimmunoprecipitation, in latently infected B cells that
219 by mass spectrometry analysis as well as RNA coimmunoprecipitation indicated differential binding of
220 ce resonance energy transfer microscopy, and coimmunoprecipitation indicated that LRRC26 was located
221                                              Coimmunoprecipitation/mass spectrometry and glutathione
222                                              Coimmunoprecipitation of CB1R protein complexes demonstr
223                                   Reciprocal coimmunoprecipitation of endogenous HeLa cell BIG1 and B
224                                 Furthermore, coimmunoprecipitation of epitope-tagged SRP72 indicated
225  the two different subunits was confirmed by coimmunoprecipitation of epitope-tagged TREK-1 and TREK-
226                                              Coimmunoprecipitation of GluN2B subunits revealed an age
227                                              Coimmunoprecipitation of green fluorescent protein-tagge
228                                              Coimmunoprecipitation of hippocampal extracts revealed t
229 ells and from virion preparations, and RIG-I coimmunoprecipitation of infected cell lysates isolated
230                                 Furthermore, coimmunoprecipitation of Jurkat cell lysates revealed th
231         With the use of specific antibodies, coimmunoprecipitation of p67(phox) and phosphorylated Pr
232                                    Chromatin coimmunoprecipitation of Piwi, the PRC2 enzymatic subuni
233 omic analysis also confirmed the interaction/coimmunoprecipitation of PSMA1-GFP with 13/14 proteasoma
234                      Sedimentation analysis, coimmunoprecipitation of recombinant proteins, and bioin
235 erminal protein (P4), which was confirmed by coimmunoprecipitation of recombinant proteins.
236 t incorporates subcellular fractionation and coimmunoprecipitation of tau from human AD and non-demen
237         These events corresponded to reduced coimmunoprecipitation of the PSD95 and KV1 proteins with
238 e SKAP55 dimerization motif (DM) enabled the coimmunoprecipitation of the Rap1-dependent integrin reg
239                     Both TM4 and TM6 blocked coimmunoprecipitation of TRAM and TLR4 ectopically expre
240                       Although TF5 prevented coimmunoprecipitation of TRIF with both TRAM and TLR4, s
241                                              Coimmunoprecipitation of Tyk2 by IL-12Rbeta1 and Jak2 by
242                                   Reciprocal coimmunoprecipitation of viral proteins from infected ce
243                                Additionally, coimmunoprecipitation of XXT2YFP and XXT5HA proteins fro
244 f this phosphorylation site does not prevent coimmunoprecipitation of yAsf1 and Rad53 from yeast extr
245                                              Coimmunoprecipitations of caveolin-3 and the voltage-gat
246           These findings in combination with coimmunoprecipitations of SEMA3A and Kv4.3 revealed a po
247 rmally in cells and was found in SAC-induced coimmunoprecipitations of the BTR complex.
248 ery after photobleaching beam-size analysis, coimmunoprecipitation, quantitative imaging, and far-Wes
249                                              Coimmunoprecipitation results indicated that gH, gL, UL1
250               Superresolution microscopy and coimmunoprecipitation reveal that ATM associates exclusi
251                                              Coimmunoprecipitation revealed diminished LPS-driven int
252                                              Coimmunoprecipitation revealed that both AP1M2 and its l
253                                              Coimmunoprecipitation revealed that FL118 slightly decre
254 the TRIF B helix residues affected TRIF-TRAM coimmunoprecipitation selectively, as these mutations di
255                                    ELISA and coimmunoprecipitation show that the TGN/endosomal small
256 esting down-regulation of Wnt signaling, and coimmunoprecipitation showed AQP1 interaction with beta-
257                                              Coimmunoprecipitation showed Cx43 being pulled down more
258                                              Coimmunoprecipitation showed that ERalpha-mGluR1 and mGl
259 ative polyacrylamide gel electrophoresis and coimmunoprecipitation showed that STIM1 in the heart exi
260                                          RNA coimmunoprecipitation showed that TTP specifically assoc
261                   Split-ubiquitin assays and coimmunoprecipitations showed interaction of MET1 with s
262                                              Coimmunoprecipitations showed that STXBP1 interacts with
263 n of type 1 PI3K with MT was demonstrated by coimmunoprecipitation, showing both PI3K subunits and in
264 was demonstrated in coimmunofluorescence and coimmunoprecipitation studies after overexpression of L2
265                                     Finally, coimmunoprecipitation studies and fluorescence microscop
266                                              Coimmunoprecipitation studies and proximity ligation ass
267             Receptor competition binding and coimmunoprecipitation studies combined with sulfo-SBED-b
268                                              Coimmunoprecipitation studies demonstrated that beta1-in
269                                              Coimmunoprecipitation studies demonstrated that KLF15 an
270               In support of this hypothesis, coimmunoprecipitation studies demonstrated that ORF2 sta
271                                              Coimmunoprecipitation studies identified Bruton tyrosine
272                                              Coimmunoprecipitation studies identified the nuclear EGR
273                                              Coimmunoprecipitation studies indicate ZMPSTE24 can comp
274  D failed to induce Akt phosphorylation, and coimmunoprecipitation studies indicated that Akt interac
275                                              Coimmunoprecipitation studies indicated that CB1R associ
276                                    These and coimmunoprecipitation studies indicated that DORs, Gbeta
277                                              Coimmunoprecipitation studies indicated that non-glycosy
278                             GST pulldown and coimmunoprecipitation studies reveal that RNF4, a RING-d
279                                              Coimmunoprecipitation studies revealed a multifaceted ro
280 play between the activities of EAAT and NCX, coimmunoprecipitation studies showed a physical interact
281                                              Coimmunoprecipitation studies showed constitutive associ
282                                              Coimmunoprecipitation studies showed that STXBP5 interac
283      Glutathione S-transferase pull-down and coimmunoprecipitation studies showed the alpha-actinin-4
284 st of these interactions are implicated from coimmunoprecipitation studies using expressed components
285 tion of LD22-4 with U87MG cells, LD22-4-NRP1 coimmunoprecipitation studies, and binding of LD22-4 to
286  AQP4 and AQP4-Delta4, which was detected in coimmunoprecipitation studies.
287                              Here we show by coimmunoprecipitation that KNOLLE forms two SNARE comple
288          We first systematically analyzed by coimmunoprecipitation the capability of 120 different G-
289 ployed live-cell imaging, gene silencing and coimmunoprecipitation to investigate the requirement of
290                                 By using RNA coimmunoprecipitation, we confirmed that a number of the
291 naptosome fractionation, immunostaining, and coimmunoprecipitation, we found that Celsr3 and Vangl2,
292     By far-Western blotting, and verified by coimmunoprecipitation, we observed that MBP-1 interacts
293                                    By MS and coimmunoprecipitation, we show that KLHL3 normally binds
294 ay, chromatin immunoprecipitation assay, and coimmunoprecipitation were exploited.
295                               MC159-IKKgamma coimmunoprecipitations were detected during infection of
296 ding Western blot, immunohistochemistry, and coimmunoprecipitation, were used to determine the expres
297                            Self-association, coimmunoprecipitation with HopBA1, and function of RBA1
298 eletion of the PLCbeta3 PDZ ligand inhibited coimmunoprecipitation with M3R and M3R-dependent PLCbeta
299  found in chorea-acanthocytosis based on Lyn coimmunoprecipitation with Ulk1 and Atg7 and on the pres
300         In this study, we combined nesprin-1 coimmunoprecipitations with mass spectrometry to identif

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