ライフサイエンスコーパス: coimmunoprecipitation

1 ation (electron microscopy) and interaction (coimmunoprecipitation).

2 UALIZED ENDOCYTIC TRAFFICKING DEFECTIVE1) by coimmunoprecipitation.

3 inase B and p38 upstream kinases as shown by coimmunoprecipitation.

4 racts with Rga7 in affinity purification and coimmunoprecipitation.

5 NaC and HDAC7 form a complex, as detected by coimmunoprecipitation.

6 by bioinformatics, immunocytochemistry, and coimmunoprecipitation.

7 tern blotting (WB), immunocytochemistry, and coimmunoprecipitation.

8 ds to Tyk2 and confirmed this interaction by coimmunoprecipitation.

9 a combination of covalent cross-linking and coimmunoprecipitation.

10 s not interact with Yap1, as demonstrated by coimmunoprecipitation.

11 cence, in situ proximity ligation assay, and coimmunoprecipitation.

12 ween chIL-17RA and chIL-17A was confirmed by coimmunoprecipitation.

13 ed membrane protein 7 (VAMP7) is detected by coimmunoprecipitation.

14 d in intact neutrophils and COSphox cells by coimmunoprecipitation.

15 case family member, by mass spectrometry and coimmunoprecipitation.

16 NEEP21 (NSG1), and ADAM10 were validated by coimmunoprecipitation.

17 cross-linking, followed by Western blot and coimmunoprecipitation.

18 binding sites and can interact with EBNA2 by coimmunoprecipitation.

19 2Shc was evaluated by proximity ligation and coimmunoprecipitations.

20 ME-DNM2 interaction was confirmed in two-way coimmunoprecipitations.

21 he interacting regions have relied mainly on coimmunoprecipitation, a technique with some pitfalls.

22 Yeast two-hybrid and coimmunoprecipitation analyses associated ANKRD1 with nu

23 vo photocross-linking along with genetic and coimmunoprecipitation analyses dissecting interactions b

24 by >30-fold), subcellular distribution, and coimmunoprecipitation analyses lead us to propose that V

25 This interaction was confirmed by coimmunoprecipitation analyses.

26 Coimmunoprecipitation analysis and proximity ligation as

27 Moreover, an unbiased proteomics screen and coimmunoprecipitation analysis identified Galphas as a n

28 Coimmunoprecipitation analysis of cholesterol-loaded cel

29 Coimmunoprecipitation analysis revealed that Mt2I286F, b

30 Coimmunoprecipitation analysis reveals for the first tim

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 We conducted coimmunoprecipitation and bimolecular fluorescence compl

34 d in planta, we further demonstrated by both coimmunoprecipitation and bimolecular fluorescence compl

35 SlCipk6 and SlRd2 interacted using coimmunoprecipitation and bimolecular fluorescence compl

36 Yeast two-hybrid, coimmunoprecipitation and bimolecular fluorescent comple

37 Further, our coimmunoprecipitation and binding studies showed that th

38 and wild-type A(1)R or A(1)R-G279S(7.44) by coimmunoprecipitation and bioluminescence resonance ener

39 the A2A receptor and SAP102 was verified by coimmunoprecipitation and by tracking its impact on rece

40 or-Galphai-GPR complex was also confirmed by coimmunoprecipitation and cell fractionation.

41 ligand blotting with CLC/Gal-10, followed by coimmunoprecipitation and coaffinity purifications.

42 tion between RRP1B and SRSF1 was verified by coimmunoprecipitation and coimmunofluorescence.

43 and have confirmed this interaction through coimmunoprecipitation and colocalization assays in the C

44 teraction was confirmed in infected cells by coimmunoprecipitation and colocalization of FAK with P i

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 satRNA was confirmed in vivo and in vitro by coimmunoprecipitation and electrophoretic mobility shift

50 Using both coimmunoprecipitation and flow-cytometric strategies, we

51 Using coimmunoprecipitation and fluorescence resonance energy

52 Coimmunoprecipitation and glutathione S-transferase (GST

53 Here, using purified recombinant proteins, coimmunoprecipitation and HDAC assays, and pulldown and

54 Coimmunoprecipitation and immunofluorescence analysis di

55 Here, we use coimmunoprecipitation and immunofluorescence microscopy

56 Coimmunoprecipitation and immunofluorescence studies rev

57 LITAF interactions were studied using coimmunoprecipitation and in situ proximity ligation ass

58 B-Raf(V600E) or K-Ras(G12C/D) Intriguingly, coimmunoprecipitation and in vitro binding assays reveal

59 alidated the mLANA-Hsc70 interaction through coimmunoprecipitation and in vitro glutathione S-transfe

60 Coimmunoprecipitation and in vitro pulldown assays revea

61 Coimmunoprecipitation and inhibition studies demonstrate

62 Using coimmunoprecipitation and live-cell imaging, we show tha

63 Coimmunoprecipitation and mass spectrometric analysis of

64 20 with dentin sialoprotein was confirmed by coimmunoprecipitation and mass spectrometry analysis of

65 Coimmunoprecipitation and mass spectrometry analysis rev

66 We reveal by coimmunoprecipitation and mass spectrometry analysis tha

67 Coimmunoprecipitation and mass spectrometry confirmed th

68 f CESA redundancy in a mutant background, by coimmunoprecipitation and mass spectrometry using label-

69 Using coimmunoprecipitation and mass spectrometry, we identifi

70 croscopy and its biochemical interactions by coimmunoprecipitation and mass spectrometry.

71 Using coimmunoprecipitation and MS, we found the cGMP-AMP synt

72 rgo complexes associated with synapsin using coimmunoprecipitation and multidimensional protein ident

73 Using coimmunoprecipitation and native gel analysis, we furthe

74 Coimmunoprecipitation and overlay experiments show that

75 Finally, coimmunoprecipitation and proximity ligation assays indi

76 we used tandem mass spectrometry followed by coimmunoprecipitation and proximity ligation assays to i

77 additional independent methodologies, i.e., coimmunoprecipitation and proximity ligation assays.

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 Coimmunoprecipitation and small RNA sequencing revealed

83 ring infection as demonstrated by reciprocal coimmunoprecipitation and supported by immunofluorescenc

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 eromeric protein complexes were validated by coimmunoprecipitation and Western blot analysis.

88 by using flow cytometry, immunofluorescence, coimmunoprecipitation, and gene expression analysis.

89 ing split luciferase complementation assays, coimmunoprecipitation, and in situ split Venus interacti

90 nvestigated using proximity ligation assays, coimmunoprecipitation, and knockdown of p300.

91 irmed by glutathione S-transferase pulldown, coimmunoprecipitation, and laser confocal microscopy ass

92 n, bimolecular fluorescence complementation, coimmunoprecipitation, and mass spectrometry analyses su

93 n, bimolecular fluorescence complementation, coimmunoprecipitation, and mass spectrometry analyses su

94 mass spectrometry, bioinformatics analysis, coimmunoprecipitation, and pull-down assays, we discover

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 Using a coimmunoprecipitation approach, we further demonstrate t

98 tion, Forster resonance energy transfer, and coimmunoprecipitation approaches revealed that SERK1 int

99 h interactive regions have relied heavily on coimmunoprecipitation approaches, whose limitations incl

100 n between LANA and RLIM could be detected in coimmunoprecipitation assay only in the presence of MG13

101 than in cycling T cells, and we detected, by coimmunoprecipitation assay, an interaction between Vpr

102 Using coimmunoprecipitation assay, we showed that BAM1 is capa

103 ed with the EBV immediate early R protein in coimmunoprecipitation assays and partially colocalized w

104 PIs were further supported by the results of coimmunoprecipitation assays and protein structural mode

105 Coimmunoprecipitation assays confirmed that GroEL protei

106 Proximity ligation and coimmunoprecipitation assays confirmed thrombin-dependen

107 In coimmunoprecipitation assays copper binding promotes APP

108 Additional two-hybrid and coimmunoprecipitation assays demonstrated that metformin

109 Furthermore, coimmunoprecipitation assays demonstrated that the two p

110 Coimmunoprecipitation assays indicated interactions betw

111 Furthermore, reciprocal coimmunoprecipitation assays revealed an association bet

112 Indeed, coimmunoprecipitation assays revealed increased interact

113 In situ and in vitro coimmunoprecipitation assays revealed that SH2D4A direct

114 Coimmunoprecipitation assays revealed the presence and i

115 more, in silico analysis in combination with coimmunoprecipitation assays show an interaction between

116 Coimmunoprecipitation assays show that TGD5 physically i

117 Coimmunoprecipitation assays showed lack of association

118 Coimmunoprecipitation assays showed TBC1D8B also interac

119 Quantitative mass spectrometry and coimmunoprecipitation assays showed that BRG1-containing

120 Moreover, coimmunoprecipitation assays showed that phosphorylation

121 bimolecular fluorescence complementation and coimmunoprecipitation assays showed that PYL4-CAR1 as we

122 abidopsis tgd1-1 Coevolutionary analysis and coimmunoprecipitation assays showed that the TGD1 L45 lo

123 Coimmunoprecipitation assays were used to examine the in

124 EKLF and PIAS proteins confirmed by in vivo coimmunoprecipitation assays with both exogenous and end

125 Moreover, in vivo coimmunoprecipitation assays with tagged Mex67 document

126 ction between HSP90 and Tax was validated by coimmunoprecipitation assays, and colocalization between

127 SIVmac239 binding to CD4 in Biacore assays, coimmunoprecipitation assays, and enzyme-linked immunoso

128 itope tagging of proteins, GST pulldown, and coimmunoprecipitation assays, and immunofluorescence and

129 demonstrate, using bacterial two-hybrid and coimmunoprecipitation assays, that endogenous LRRFIP1 (L

130 On the basis of yeast two-hybrid and coimmunoprecipitation assays, we demonstrate here that N

131 Using coimmunoprecipitation assays, we demonstrate that the Y1

132 By using mass spectrometry analysis and coimmunoprecipitation assays, we show here that VP35 is

133 Using a yeast two-hybrid screen and coimmunoprecipitation assays, we showed that Fignl1 bind

134 n was confirmed by both peptide pulldown and coimmunoprecipitation assays, which also demonstrated th

135 Env and Zfp111 was confirmed through in vivo coimmunoprecipitation assays.

136 bimolecular fluorescence complementation and coimmunoprecipitation assays.

137 tide was sufficient for M protein binding in coimmunoprecipitation assays.

138 xes that are stable enough to be captured in coimmunoprecipitation assays.

139 To address this, we performed a coimmunoprecipitation-based proteomics screen to identif

140 By coimmunoprecipitation, BET proteins were found to be com

141 Our data clearly showed that coimmunoprecipitation between AtMC1 and AtSerpin1 and fo

142 Acute beta-AR activation increases coimmunoprecipitation between P-RyR and cardiac spliced

143 omplementary inactive AR mutants and promote coimmunoprecipitation between unlike forms of AR suggest

144 Two-step coimmunoprecipitation (co-IP) and fluorescence resonance

145 identified binding partners of MATalpha1 by coimmunoprecipitation (co-IP) and mass spectrometry.

146 unctions, we used two complementary methods, coimmunoprecipitation (co-IP) and proximity biotinylatio

147 ractions, we used two independent untargeted coimmunoprecipitation (co-IP) approaches with the biosyn

148 , we developed in vivo beta-importin complex coimmunoprecipitation (co-IP) assays using budding yeast

149 Mass spectrometry analysis and coimmunoprecipitation (co-IP) identified a direct intera

150 hromatin immunoprecipitation (ChIP), protein coimmunoprecipitation (Co-IP), and bimolecular fluoresce

151 Studies using coimmunoprecipitation (co-IP), bimolecular fluorescence

152 experimental and computational methods for a coimmunoprecipitation (Co-IP)-based workflow from sample

153 Coimmunoprecipitation, coimmunolocalization, and ChIP an

154 Coimmunoprecipitation (coIP) and anisotropy-based FRET (

155 of lepidopteran microtubule transport using coimmunoprecipitation, colocalization, yeast two-hybrid,

156 Coimmunoprecipitation confirmed a physical interaction b

157 PPP1R3A as a novel RyR2-binding partner, and coimmunoprecipitation confirmed PPP1R3A binding to RyR2

158 Coimmunoprecipitation confirmed the interaction between

159 at AVR1 and Sec5 are in close proximity, and coimmunoprecipitation confirmed the interaction.

160 Coimmunoprecipitation demonstrated protein-protein inter

161 Coimmunoprecipitation demonstrated that XB130 and Tks5 i

162 Coimmunoprecipitation detected binding of phosphorylated

163 We reveal by coimmunoprecipitation, Duolink proximity ligation assay,

164 underlying this metabolic association, using coimmunoprecipitation, electrophysiologic measurements,

165 he ERBB4-VAV3 interaction by targeted MS and coimmunoprecipitation experiments and further defined it

166 Coimmunoprecipitation experiments and in vitro assays pr

167 By coimmunoprecipitation experiments and mass spectrometry,

168 Coimmunoprecipitation experiments and proximity ligation

169 Yeast two-hybrid assays and coimmunoprecipitation experiments confirm the structural

170 Coimmunoprecipitation experiments confirmed interaction

171 Immunoprecipitation/mass spectrometry and coimmunoprecipitation experiments confirmed that PLD4 bi

172 GST-based pulldowns and coimmunoprecipitation experiments demonstrate preferenti

173 Coimmunoprecipitation experiments demonstrated loss of p

174 Coimmunoprecipitation experiments demonstrated that RBPG

175 Coimmunoprecipitation experiments demonstrated that thes

176 Moreover, coimmunoprecipitation experiments from rat DRG lysates i

177 Proteomic and coimmunoprecipitation experiments identified pontin as a

178 Coimmunoprecipitation experiments in HEK293 cells reveal

179 s on NCC, and conducted yeast two-hybrid and coimmunoprecipitation experiments in NCC-expressing MDCK

180 Coimmunoprecipitation experiments in these tomato plants

181 Coimmunoprecipitation experiments indicate that two-thir

182 Coimmunoprecipitation experiments indicated that 5LO-CLP

183 Coimmunoprecipitation experiments indicated that AMPK le

184 r gH/UL116 complex formation was obtained by coimmunoprecipitation experiments on both transfected an

185 , electrophoretic mobility shift assays, and coimmunoprecipitation experiments reveal a specific inte

186 bioinformatics analyses, sequential ChIP and coimmunoprecipitation experiments reveal that Atro inter

187 Coimmunoprecipitation experiments revealed an interactio

188 IL13Ralpha2-FAM120A coimmunoprecipitation experiments revealed further signa

189 Coimmunoprecipitation experiments revealed that CO inhib

190 Coimmunoprecipitation experiments revealed that core doe

191 Coimmunoprecipitation experiments revealed that the majo

192 Coimmunoprecipitation experiments revealed that the ORF3

193 imolecular fluorescence complementation, and coimmunoprecipitation experiments show that DRB3 acts do

194 ively parallel DNA sequencing (ChIP-seq) and coimmunoprecipitation experiments show that LIN28B binds

195 Coimmunoprecipitation experiments showed that BMAA treat

196 Coimmunoprecipitation experiments showed that Hsp90 inte

197 Coimmunoprecipitation experiments showed that TnBVANK1 b

198 Coimmunoprecipitation experiments suggested that endogen

199 hmwBP complex was corroborated by reciprocal coimmunoprecipitation experiments using antipeptide anti

200 n SH3 binding domain, immunofluorescence and coimmunoprecipitation experiments were conducted and rev

201 Coimmunoprecipitation experiments were used to demonstra

202 7 (aa 693 to 982) was identified by fragment coimmunoprecipitation experiments, and a head-to-tail se

203 romoter reporter and in vitro kinase assays, coimmunoprecipitation experiments, and confocal microsco

204 directed mutagenesis, GTP hydrolysis assays, coimmunoprecipitation experiments, and structural analys

205 A time course study of import, followed by coimmunoprecipitation experiments, confirmed that Hsp93

206 Using coimmunoprecipitation experiments, identification of bou

207 Here we have used coimmunoprecipitation experiments, protein turnover and

208 in chloroplast protein homeostasis based on coimmunoprecipitation experiments.

209 nd endogenous M3R interacted with PLCbeta in coimmunoprecipitation experiments.

210 observed in both yeast two-hybrid assays and coimmunoprecipitation experiments.

211 kA N-terminal deletion mutants and performed coimmunoprecipitation experiments.

212 ble subunit alpha-2 using colocalization and coimmunoprecipitation experiments.

213 tion between apoE and Abeta was confirmed by coimmunoprecipitation experiments.

214 Yet, by coimmunoprecipitation, fluorescence microscopy, and a pr

215 Using coimmunoprecipitation, followed by mass spectrometry, we

216 east-two hybrid assay, in vitro binding, and coimmunoprecipitation from mouse spermatocytes, we ident

217 Moreover, MRTF-A and YAP associate in coimmunoprecipitations from S1P-stimulated cells.

218 ions (PPIs), such as in vitro pull downs and coimmunoprecipitations, have become popular in most labo

219 Coimmunoprecipitation identified a series of ERICH3 inte

220 Coimmunoprecipitation-immunoblot analyses in the presenc

221 Coimmunoprecipitation, immunofluorescent, and electrophy

222 ed protein 97 (SAP97; also known as DLG1) by coimmunoprecipitation in human embryonic 293 (HEK 293) c

223 -G, both in yeast two-hybrid analysis and by coimmunoprecipitation in situ in HEK293 cells expressing

224 ership of UGT1A_i2 and PKM2 was confirmed by coimmunoprecipitation in the HT115 colon cancer cells an

225 As indicated by coimmunoprecipitation, in latently infected B cells that

226 by mass spectrometry analysis as well as RNA coimmunoprecipitation indicated differential binding of

227 ce resonance energy transfer microscopy, and coimmunoprecipitation indicated that LRRC26 was located

228 Coimmunoprecipitation, mass spectrometry, and bioinforma

229 Coimmunoprecipitation/mass spectrometry and glutathione

230 Coimmunoprecipitation of CB1R protein complexes demonstr

231 the two different subunits was confirmed by coimmunoprecipitation of epitope-tagged TREK-1 and TREK-

232 Coimmunoprecipitation of green fluorescent protein-tagge

233 Coimmunoprecipitation of hippocampal extracts revealed t

234 ells and from virion preparations, and RIG-I coimmunoprecipitation of infected cell lysates isolated

235 This differential binding was confirmed via coimmunoprecipitation of overexpressed FBXW7 and NOTCH1.

236 Chromatin coimmunoprecipitation of Piwi, the PRC2 enzymatic subuni

237 Sedimentation analysis, coimmunoprecipitation of recombinant proteins, and bioin

238 erminal protein (P4), which was confirmed by coimmunoprecipitation of recombinant proteins.

239 te and mononuclear library) and confirmed by coimmunoprecipitation of tagged and endogenous proteins.

240 t incorporates subcellular fractionation and coimmunoprecipitation of tau from human AD and non-demen

241 These events corresponded to reduced coimmunoprecipitation of the PSD95 and KV1 proteins with

242 e SKAP55 dimerization motif (DM) enabled the coimmunoprecipitation of the Rap1-dependent integrin reg

243 Coimmunoprecipitation of Tyk2 by IL-12Rbeta1 and Jak2 by

244 Reciprocal coimmunoprecipitation of viral proteins from infected ce

245 their direct interaction in vitro Moreover, coimmunoprecipitation of ZFP628 and TAF4b proteins in te

246 Coimmunoprecipitations of caveolin-3 and the voltage-gat

247 These findings in combination with coimmunoprecipitations of SEMA3A and Kv4.3 revealed a po

248 of action of LGR4 and LGR5 in parallel using coimmunoprecipitation, proximity ligation, competition b

249 Coimmunoprecipitation results indicated that gH, gL, UL1

250 Superresolution microscopy and coimmunoprecipitation reveal that ATM associates exclusi

251 Coimmunoprecipitation revealed that FL118 slightly decre

252 Coimmunoprecipitation revealed that stretch promoted an

253 We show by RNA coimmunoprecipitation sequencing (RIP-seq) that artifici

254 ELISA and coimmunoprecipitation show that the TGN/endosomal small

255 esting down-regulation of Wnt signaling, and coimmunoprecipitation showed AQP1 interaction with beta-

256 Coimmunoprecipitation showed Cx43 being pulled down more

257 Coimmunoprecipitation showed that ERalpha-mGluR1 and mGl

258 ative polyacrylamide gel electrophoresis and coimmunoprecipitation showed that STIM1 in the heart exi

259 RNA coimmunoprecipitation showed that TTP specifically assoc

260 Split-ubiquitin assays and coimmunoprecipitations showed interaction of MET1 with s

261 Coimmunoprecipitations showed that STXBP1 interacts with

262 n of type 1 PI3K with MT was demonstrated by coimmunoprecipitation, showing both PI3K subunits and in

263 was demonstrated in coimmunofluorescence and coimmunoprecipitation studies after overexpression of L2

264 Finally, coimmunoprecipitation studies and fluorescence microscop

265 Coimmunoprecipitation studies and proximity ligation ass

266 Coimmunoprecipitation studies are consistent with an int

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 NA interactome, RNA immunoprecipitation, and coimmunoprecipitation studies identified BCALM-interacti

272 Coimmunoprecipitation studies identified Bruton tyrosine

273 Coimmunoprecipitation studies identified the nuclear EGR

274 Moreover, our coimmunoprecipitation studies in monocytes revealed that

275 Coimmunoprecipitation studies indicate ZMPSTE24 can comp

276 Coimmunoprecipitation studies indicated that CB1R associ

277 Coimmunoprecipitation studies indicated that non-glycosy

278 panded gene family in C. elegans Here we use coimmunoprecipitation studies paired with genetic analys

279 Chromatin immunoprecipitation and protein coimmunoprecipitation studies provided evidence that TCF

280 rnal reflection fluorescence microscopy, and coimmunoprecipitation studies reveal that IGF1R associat

281 Coimmunoprecipitation studies revealed a multifaceted ro

282 Immunofluorescence and coimmunoprecipitation studies revealed an interaction be

283 Coimmunoprecipitation studies showed constitutive associ

284 Coimmunoprecipitation studies showed that STXBP5 interac

285 Glutathione S-transferase pull-down and coimmunoprecipitation studies showed the alpha-actinin-4

286 st of these interactions are implicated from coimmunoprecipitation studies using expressed components

287 AQP4 and AQP4-Delta4, which was detected in coimmunoprecipitation studies.

288 We first systematically analyzed by coimmunoprecipitation the capability of 120 different G-

289 inds to Smad3 in human pulmonary artery SMC (coimmunoprecipitation), thereby blocking its phosphoryla

290 ployed live-cell imaging, gene silencing and coimmunoprecipitation to investigate the requirement of

291 versions of the proteins were refractory to coimmunoprecipitation under mild-detergent conditions.

292 naptosome fractionation, immunostaining, and coimmunoprecipitation, we found that Celsr3 and Vangl2,

293 Using tandem mass spectrometry and coimmunoprecipitation, we identified the kinase zeta-ass

294 By far-Western blotting, and verified by coimmunoprecipitation, we observed that MBP-1 interacts

295 ding Western blot, immunohistochemistry, and coimmunoprecipitation, were used to determine the expres

296 Self-association, coimmunoprecipitation with HopBA1, and function of RBA1

297 eletion of the PLCbeta3 PDZ ligand inhibited coimmunoprecipitation with M3R and M3R-dependent PLCbeta

298 found in chorea-acanthocytosis based on Lyn coimmunoprecipitation with Ulk1 and Atg7 and on the pres

299 In this study, we combined nesprin-1 coimmunoprecipitations with mass spectrometry to identif

300 ization, glutathione S-transferase pulldown, coimmunoprecipitation, yeast two-hybrid, gel shift, and