ライフサイエンスコーパス: immunoprecipitation

1 irmed by protein structure prediction and co-immunoprecipitation.

2 ndard" chromatin assays, including chromatin immunoprecipitation.

3 ation with intact LTCC complexes isolated by immunoprecipitation.

4 riptase (qRT)-PCR, zymography, and chromatin immunoprecipitation.

5 XR1 by using a BioID proximity assay and RNA immunoprecipitation.

6 3 and Osx in odontoblasts was detected by co-immunoprecipitation.

7 70-kDa protein, and OGT were confirmed by co-immunoprecipitation.

8 e TFIID subunit coactivator TAF4 assessed by immunoprecipitation.

9 1) was validated using RNA pull-down and RNA immunoprecipitation.

10 electrophoretic mobility assay and chromatin immunoprecipitation.

11 or inflammatory factors was measured by RNA immunoprecipitation.

12 promoter was examined in NAc using chromatin immunoprecipitation after repeated cocaine.

13 ine direct targets, we performed a chromatin immunoprecipitation against Lmx1b in mouse limbs at embr

14 Chromatin immunoprecipitation analyses demonstrated that these gen

15 Chromatin immunoprecipitation analyses of liver tissue showed that

16 Notably, biochemical and chromatin immunoprecipitation analyses reveal constitutive binding

17 ioinformatics, reporter assay, and chromatin immunoprecipitation analyses, we found that NFkappaB and

18 ble ribonucleoside-enhanced crosslinking and immunoprecipitation analyses.

19 Chromatin immunoprecipitation analysis confirmed that clofibrate a

20 Finally, chromatin immunoprecipitation analysis confirmed that Lyn overexpr

21 Immunoprecipitation analysis demonstrated that ATP incre

22 However, chromatin immunoprecipitation analysis in embryonic stem cells sho

23 ophoretic mobility shift assay and chromatin immunoprecipitation analysis indicated that Klf5 bound t

24 Furthermore, chromatin immunoprecipitation analysis revealed that OA-NO2 increa

25 oter was demonstrated by EMSAs and chromatin immunoprecipitation analysis, suggesting transcriptional

26 ver regeneration using genome-wide chromatin immunoprecipitation analysis.

27 changes to hnRNP K metabolism by RNA binding immunoprecipitation analysis.

28 Using co-immunoprecipitation and (55)Fe-radiolabeling experiments

29 d ilp8) are putative targets of miR-277; RNA immunoprecipitation and a luciferase reporter assay conf

30 Using yeast two-hybrid, GST pull-down, co-immunoprecipitation and bimolecular florescence compleme

31 Co-immunoprecipitation and biochemical fractionation data s

32 n between sigma1R and DAT was detected by co-immunoprecipitation and bioluminescence resonance energy

33 Using co-immunoprecipitation and CDK kinase activity assays, we f

34 The results from our immunoprecipitation and cell culture experiments showed

35 yed for beta-catenin activity and studied in immunoprecipitation and chromatin immunoprecipitation as

36 We performed co-immunoprecipitation and chromatin immunoprecipitation ex

37 TRIM24) and confirmed this interaction by co-immunoprecipitation and co-immunostaining.

38 Immunoprecipitation and ELISA-style binding assays confi

39 tions in the tru1 gene as shown by chromatin immunoprecipitation and gel shifts.

40 antly with kinesin light chain (KLC-1/2) and immunoprecipitation and GST pull-down showed that these

41 Immunoprecipitation and immunofluorescence experiments r

42 In vitro co-immunoprecipitation and in vivo colocalization experimen

43 Chromatin immunoprecipitation and luciferase reporter assays revea

44 ainst human Mregs was identified as DHRS9 by immunoprecipitation and MALDI-MS sequencing.

45 uman trophoblast-derived cells by performing immunoprecipitation and mammalian one hybrid assays.

46 Immunoprecipitation and mass spectrometry of the EZH2-pr

47 Here we used immunoprecipitation and mass spectrometry to identify hu

48 We have used co-immunoprecipitation and mass spectrometry to identify pr

49 protein 2 (LRP2), also known as megalin, by immunoprecipitation and mass spectrometry.

50 Chromatin immunoprecipitation and NNMT promoter luciferase assays

51 n blot, reverse-transcriptase PCR, chromatin immunoprecipitation and promoter reporter assays.

52 Co-immunoprecipitation and proximity ligation assay (Duolin

53 Using co-immunoprecipitation and proximity ligation assays on end

54 Immunocytochemistry, co-immunoprecipitation and proximity ligation assays reveal

55 Co-immunoprecipitation and pulldown assays confirmed PKC an

56 In immunoprecipitation and pulldown assays, ShcA, via its S

57 novel molecular assay, ChIPnQASO (Chromatin Immunoprecipitation and Quantitative Allele-Specific Occ

58 terature, based on next generation chromatin immunoprecipitation and RNA sequencing of reward brain r

59 UV crosslinking immunoprecipitation and sequencing (CLIP-seq) identify R

60 Finally, our ribonucleoprotein immunoprecipitation and sequencing (RIP-seq) analyses of

61 Chromatin immunoprecipitation and sequencing analysis revealed inc

62 Chromatin immunoprecipitation and sequencing experiments revealed

63 Immunoprecipitation and simultaneous assay by Western bl

64 In line with this interpretation, co-immunoprecipitation and SPR experiments indicated that E

65 mma-catenin and actin was demonstrated in co-immunoprecipitation and surface plasmon resonance experi

66 Using RNA immunoprecipitation and UV cross-linking, we show that W

67 lymerase chain reaction, (far) Western blot, immunoprecipitation, and immunocytochemistry were used t

68 such as RNA sequencing (RNA-Seq), chromatin immunoprecipitation, and ribosome profiling.

69 cal microscopy, quantitative image analysis, immunoprecipitation, and RT-qPCR.

70 were investigated by native electrophoresis, immunoprecipitation, and sucrose density centrifugation.

71 ical interaction between HDAC4/Rad51/Ubc9 by immunoprecipitation; and the downstream targets of HDAC4

72 his end, we performed Argonaute crosslinking immunoprecipitation (Argonaute [Ago]-CLIP) sequencing in

73 A chromatin immunoprecipitation assay confirmed that hypermethylatio

74 Moreover, a chromatin immunoprecipitation assay demonstrated that MYC binds to

75 Double immunostaining and an immunoprecipitation assay revealed that TB4 interacted w

76 Furthermore, as measured in a co-immunoprecipitation assay, substitution of the His or Cy

77 This was further confirmed by co-immunoprecipitation assay.

78 Chromatin immunoprecipitation assays and PCR analysis confirmed HN

79 Chromatin immunoprecipitation assays confirmed that hyperglycemia

80 By using quantitative co-immunoprecipitation assays coupled with tandem mass spec

81 Immunoprecipitation assays demonstrated that the PARP-1

82 Luciferase reporter and chromatin immunoprecipitation assays demonstrated that TSPAN2 is r

83 Chromatin immunoprecipitation assays indicated that KAT8 regulates

84 Chromatin immunoprecipitation assays indicated that PAF-treatment

85 In silico analysis and chromatin immunoprecipitation assays revealed that the downstream

86 RD4, an important BET protein, and chromatin immunoprecipitation assays showed that JQ1 alters the di

87 treated with or without T3 and for chromatin immunoprecipitation assays with these chips, we determin

88 TPase activity, luciferase assays, chromatin immunoprecipitation assays, and network analyses were us

89 Employing immunoprecipitation assays, hRETNTg(+)Tlr4(-/-) mice, an

90 We also used immunoprecipitation assays, immunoblotting, and an in si

91 In chromatin immunoprecipitation assays, p65 bound directly to the pr

92 ediated transcriptome analysis and chromatin immunoprecipitation assays, suggesting that MYB112 may b

93 electrophoretic mobility shift and chromatin immunoprecipitation assays, that phosphorylation of YY1

94 Using luciferase and chromatin immunoprecipitation assays, we demonstrate that GLI2 dir

95 combination of yeast 2-hybrid screens and co-immunoprecipitation assays.

96 studied in immunoprecipitation and chromatin immunoprecipitation assays.

97 bunit p65 in cells was analyzed in chromatin immunoprecipitation assays.

98 EDNRB gene in transactivation and chromatin immunoprecipitation assays; results were validated in fu

99 s from peaks identified by Ago2 Cross-Linked ImmunoPrecipitation associated to high-throughput sequen

100 plicing and performed quantitative chromatin immunoprecipitation at downstream targets in NAc followi

101 xpression, transposition activity, chromatin immunoprecipitation at the target loci, and targeted kno

102 ination of fluorescence polarization- and co-immunoprecipitation-based assays, we establish that bind

103 hensive analysis of bisulfite conversion and immunoprecipitation-based methylation and hydroxymethyla

104 However, we did not observe co-immunoprecipitation between Nedd4L and NKCC1, suggesting

105 tion of elongation rate in vivo by chromatin immunoprecipitation can be confounded by the kinetics an

106 We show through chromatin immunoprecipitation (ChIP) and chemical inhibitor studie

107 Chromatin immunoprecipitation (ChIP) and chromatin isolation by RN

108 Chromatin immunoprecipitation (ChIP) and micrococcal nuclease (MNa

109 L4 transcription, we quantified by chromatin immunoprecipitation (ChIP) assays RNA polymerase II occu

110 ffymetrix microarray profiling and chromatin immunoprecipitation (ChIP) assays, we found that ALOX5 i

111 hich houses the annotation of 1870 chromatin immunoprecipitation (ChIP) datasets of 585 TFs in five s

112 The validation with the chromatin immunoprecipitation (ChIP) sequencing (ChIP-Seq) data sh

113 Chromatin immunoprecipitation (ChIP) studies illustrated that M in

114 is a transcription factor, we used chromatin immunoprecipitation (ChIP) to assess PDC's ability to in

115 ic mobility shift assay (EMSA) and chromatin immunoprecipitation (ChIP), we found evidence for the NR

116 Unlike Chromatin Immunoprecipitation (ChIP), which fragments and solubili

117 Chromatin immunoprecipitation (ChIP-seq) is the omics technique th

118 ChIP-seq (chromatin immunoprecipitation [ChIP] combined with high-throughput

119 Here, we leveraged p53 ChIP-seq (chromatin immunoprecipitation [ChIP] combined with high-throughput

120 ChIP-seq (chromatin immunoprecipitation [ChIP] followed by deep sequencing)

121 Here we used cross-linking immunoprecipitation (CLIP) and ligation of miRNA-target

122 UV cross-linking and immunoprecipitation (CLIP), followed by high-throughput

123 Using co-immunoprecipitation combined with mass spectrometry and

124 To identify putative CD47 interactants, immunoprecipitation combined with Nano LC-MS/MS mass spe

125 Immunoprecipitation confirmed that DPP4 is displayed on

126 Surface plasmon resonance and co-immunoprecipitation confirmed that recombinant human TSP

127 Using immunoprecipitation coupled with mass spectrometry and i

128 decreased H3K27me3 as revealed by chromatin immunoprecipitation coupled with quantitative polymerase

129 Our binding, competition, and immunoprecipitation data corroborate and elaborate on th

130 ilico analysis in conjunction with chromatin immunoprecipitation demonstrated MADS-RIN protein bindin

131 Chromatin immunoprecipitation, DNase I hypersensitivity and transp

132 ys, sucrose density gradient centrifugation, immunoprecipitation, dot and Western blotting, and confo

133 ered DNA-binding molecule-mediated chromatin immunoprecipitation (enChIP), coupled with mass spectrom

134 expression, the magnitude of SHB1 chromatin immunoprecipitation enrichment and the over-representati

135 Analysis by the chromatin immunoprecipitation-exonuclease (ChIP-exo) method allowe

136 T-type channels associate with CaM using co-immunoprecipitation experiments and single particle cryo

137 Co-immunoprecipitation experiments demonstrated that Cx43-b

138 Integration of omics data and RNA immunoprecipitation experiments established DGCR8 as a d

139 Pulldown and co-immunoprecipitation experiments identified the ArfGAP wi

140 tion factor-DNA-binding arrays and chromatin immunoprecipitation experiments identified the formation

141 r fluorescence complementation (BiFC) and co-immunoprecipitation experiments indicated that CERK1 phy

142 Immunoprecipitation experiments performed in transfected

143 In co-immunoprecipitation experiments performed on H2O2-treate

144 FLAG-immunoprecipitation experiments retrieve a ferrochelatas

145 Chromatin immunoprecipitation experiments reveal increased binding

146 To map Coy1 protein interactions, co-immunoprecipitation experiments revealed an association

147 Chromatin immunoprecipitation experiments revealed that a wide reg

148 Additional co-immunoprecipitation experiments revealed that FGF13 pote

149 Surprisingly, immunoprecipitation experiments revealed that FX and PTX

150 Chromatin-immunoprecipitation experiments showed that HES1 and NR3

151 Co-immunoprecipitation experiments suggested that these ubi

152 d with 2xhemagglutinin allowed us to perform immunoprecipitation experiments that showed that MceA fo

153 By co-immunoprecipitation experiments we found that PC1 trunca

154 or the autoinhibition model, we performed co-immunoprecipitation experiments with combinations of ART

155 This was supported by co-immunoprecipitation experiments, where membrane-bound di

156 cytoskeleton organization and binds actin in immunoprecipitation experiments.

157 rformed co-immunoprecipitation and chromatin immunoprecipitation experiments.

158 -like receptor 4 (TLR4) was determined by co-immunoprecipitation, fluorescein isothiocyanate-probing,

159 Using crosslinking and immunoprecipitation followed by deep sequencing (ChIP-se

160 or efficient generation of histone chromatin immunoprecipitation followed by deep sequencing (ChIP-se

161 c acid sequencing datasets such as chromatin immunoprecipitation followed by deep sequencing (ChIP-se

162 Chromatin immunoprecipitation followed by deep sequencing (ChIP-se

163 h PBM through Argonaute 1 cross-linking and immunoprecipitation followed by high-throughput sequenci

164 Immunoprecipitation followed by mass spectrometry analys

165 and ALS-linked MATR3 mutations, we performed immunoprecipitation followed by mass spectrometry using

166 Chromatin immunoprecipitation followed by massively parallel DNA s

167 HuR ribonucleoprotein immunoprecipitation followed by microarray (RIP-chip) an

168 ntial ISE2 substrates were identified by RNA immunoprecipitation followed by next-generation sequenci

169 Using chromatin immunoprecipitation followed by next-generation sequenci

170 Chromatin immunoprecipitation followed by sequencing (ChIP-Seq) ha

171 d 214 public datasets representing chromatin immunoprecipitation followed by sequencing (ChIP-Seq) of

172 Crosslinking or RNA immunoprecipitation followed by sequencing (CLIP-seq or

173 and crystal structural studies and chromatin-immunoprecipitation followed by sequencing analyses reve

174 lysine 27 of histone H3 (H3K27me3) chromatin immunoprecipitation followed by sequencing identify 76 g

175 mmon scenario of ERG upregulation, chromatin immunoprecipitation followed by sequencing indicates tha

176 Genome-wide analysis of chromatin immunoprecipitation followed by sequencing reveals that

177 ours after surgery and analyzed by chromatin immunoprecipitation followed by sequencing.

178 Using immunoprecipitation, followed by MS, we identified a tra

179 By chromatin immunoprecipitation FOXO1 was shown to bind to the MMP9

180 After an exposure event, immunoprecipitation from blood with a BChE-specific anti

181 l-nucleotide resolution UV cross-linking and immunoprecipitation (hiCLIP) is a transcriptome-wide met

182 Chromatin immunoprecipitation high-throughput sequencing (ChIP-seq

183 t sequencing of RNA isolated by crosslinking immunoprecipitation (HITS-CLIP), we identified the vRNA

184 ning individual-resolution cross-linking and immunoprecipitation (iCLIP) and mass spectrometry, we sh

185 nsfer, immunofluorescence microscopy, and co-immunoprecipitation in cells expressing receptors exogen

186 cessible chromatin sequencing, and chromatin immunoprecipitation in human umbilical vein endothelial

187 isiae Mediator from chromatin with chromatin immunoprecipitation in order to reveal Mediator occupanc

188 tion experiments by using immunoblotting and immunoprecipitation in STAT1-deficient cell lines.

189 Reciprocal immunoprecipitations indicated that TCTP forms complexes

190 However, in our immunoprecipitation (IP) experiments, we did not observe

191 The combination of immunoprecipitation (IP) with MALDI technology delivers

192 or screening, small interfering RNA (siRNA), immunoprecipitation (IP), immunoblots and bioinformatics

193 exes interacting with the specific RBP using immunoprecipitation; ligation of the two arms of RNA dup

194 Using differential immunoprecipitation, mass spectrometry and a stringent f

195 anisms were investigated by RNA pulldown and immunoprecipitation, mass spectrometry, microarray, seve

196 Finally, immunoprecipitation-mass spectrometry analyses using PTH

197 Immunoprecipitation-mass spectrometry identified ribosom

198 Immunoprecipitation/mass spectrometry and coimmunoprecip

199 zyme-substrate interactions, conventional co-immunoprecipitation methods frequently fail to identify

200 Subsequently, co-immunoprecipitation of Ang-1 and CD18 demonstrated their

201 Immunoprecipitation of ARC from mouse islet lysates show

202 Performing immunoprecipitation of bromouridine-labeled p21 mRNAs th

203 not in IS5S6 or in IIS5S6, prevented the co-immunoprecipitation of CaV1.2 with CaValpha2delta1.

204 Using immunoprecipitation of COPII vesicles and immunogold ele

205 Nbeal2 with additional validation by reverse immunoprecipitation of Dock7, Sec16a, and Vac14 as inter

206 aturally presented peptides was performed by immunoprecipitation of HLA and subsequent analysis of HL

207 the 1,25(OH)2D target gene CYP24A1 involved immunoprecipitation of hnRNPC1/C2 with CYP24A1 chromatin

208 Finally, addition of DRB reduces co-immunoprecipitation of ICP27 using an anti-SPT5 antibody

209 Immunoprecipitation of isoform 2 validated a binding aff

210 substitution of Thr-38 with Asp increased co-immunoprecipitation of the CAR DBD with CAR LBD in Huh-7

211 lar localization of the MybA::Gfp fusion and immunoprecipitation of the MybA::Gfp or MybA::3xHa prote

212 action with the E3 ubiquitin ligase HRD1, as immunoprecipitation of Tomo-1 from neurons co-precipitat

213 truct containing an MS2-binding site, and by immunoprecipitation of WIG1 and detection of WIG1-associ

214 Through immunoprecipitation of YY1-bound chromatin from affected

215 d gene regions (DMRs) using a methylated DNA immunoprecipitation on chip (MeDIP-chip).

216 We performed chromatin immunoprecipitation on reporter genes containing these e

217 r, we developed an oligonucleotide retrieval immunoprecipitation (ORiP) assay using a novel platinate

218 ble ribonucleoside-enhanced crosslinking and immunoprecipitation (PAR-CLIP), we isolated RNAs associa

219 Chromatin immunoprecipitation-PCR detected increased ETS1 and hist

220 the Human Phospho-Kinase Array and chromatin immunoprecipitation-PCR revealed that unlike GBMDC, PRMT

221 e apply permanganate treatment and chromatin immunoprecipitation (PIP-seq) of initiation factors to i

222 product ions, collected over 23 independent immunoprecipitation preparations, established method ope

223 We then optimized a Gag immunoprecipitation procedure that permitted sampling of

224 Findings from co-immunoprecipitation, protein-fragment complementation, a

225 Chromatin-Immunoprecipitation-qPCR and electrophoretic mobility sh

226 pitation sequencing (ChIP-seq) and chromatin immunoprecipitation quantitative PCR (ChIP-qPCR) indicat

227 to identify targets of MIR122 and chromatin immunoprecipitation quantitative polymerase chain reacti

228 Furthermore, chromatin immunoprecipitation-quantitative PCR assay showed enrich

229 Moreover, ENCODE data and our chromatin immunoprecipitation results indicate that cohesin is alm

230 Immunoprecipitation revealed interaction of NLRP1 with C

231 Chromatin immunoprecipitation revealed that H3K4me3, the target of

232 Chromatin immunoprecipitation revealed that MYST3 binds to the pro

233 Cross-linking immunoprecipitation revealed that Pum1 and Pum2 bind to

234 METHODS AND RNA immunoprecipitation revealed the involvement of CELF1-re

235 In vivo RNA immunoprecipitation (RIP) assays revealed that SFPS asso

236 We integrated sequencing data from chromatin immunoprecipitation, RNA expression, DNA methylation, an

237 RNA immunoprecipitation-RNAseq (RIP-Seq) identified transcri

238 chromatin immunoprecipitation-seq analyses of NRSF targets identif

239 Chromatin immunoprecipitation sequencing (ChIP-seq) and chromatin

240 Using chromatin immunoprecipitation sequencing (ChIP-seq) combined with

241 Chromatin immunoprecipitation sequencing (ChIP-seq) experiments sh

242 in primary response, making use of chromatin immunoprecipitation sequencing (ChIP-seq), protein-bindi

243 a from related experiments such as Chromatin Immunoprecipitation sequencing (ChIP-Seq).

244 nsive, and more easily scaled than chromatin immunoprecipitation sequencing (ChIP-seq).

245 In addition, chromatin immunoprecipitation sequencing analyses showed that a su

246 Gene profiling and chromatin immunoprecipitation sequencing analyses unraveled a tran

247 Chromatin immunoprecipitation sequencing analysis with immnolocali

248 Chromatin immunoprecipitation sequencing and gene expression profi

249 d these profiles with whole-animal chromatin immunoprecipitation sequencing data to deconvolve the ce

250 Using RNA-sequencing and chromatin immunoprecipitation sequencing experiments, we show that

251 OCK in human neurons by performing chromatin immunoprecipitation sequencing for endogenous CLOCK in a

252 whole-transcriptome sequencing and chromatin immunoprecipitation sequencing pinpointed oncogenic tran

253 Furthermore, microarray and chromatin immunoprecipitation sequencing screens led to the discov

254 ole of Rbfox2 in stress granules we used RNA-immunoprecipitation sequencing to identify cytoplasmic t

255 es for the study of the epigenome (chromatin immunoprecipitation sequencing) and transcriptome (RNA s

256 dopsis seedlings were generated by chromatin immunoprecipitation sequencing, and changes induced by G

257 However, most chromatin immunoprecipitation-sequencing (ChIP-seq) analyses have

258 using epigenetic data derived from chromatin immunoprecipitation-sequencing (ChIP-Seq).

259 Genome-wide chromatin immunoprecipitation-sequencing analysis reveals that LSD

260 were identified by integration of chromatin immunoprecipitation-sequencing and RNA-sequencing data.

261 Reciprocal co-immunoprecipitations show that KhpA forms a complex in c

262 Immunoprecipitation showed enhanced Rac1-bound 11beta-HS

263 Chromatin immunoprecipitation showed PPAR-gamma binding to the TRP

264 Chromatin immunoprecipitation showed that C/EBPbeta was recruited

265 Chromatin immunoprecipitation showed that further induction of Mmp

266 RNA-immunoprecipitation showed that KhpA/KhpB bind an overla

267 Immunoprecipitation showed that PTST2 interacts with STA

268 Chromatin immunoprecipitation showed the presence of HDAC11 at the

269 demethylation was tested by using chromatin immunoprecipitation, small interfering RNA-mediated down

270 By chromatin immunoprecipitation, STAT1 bound a putative regulatory s

271 The complexity and inefficiency of chromatin immunoprecipitation strategies restrict their sensitivit

272 scopy, western blotting, gel filtration, and immunoprecipitation studies in macrophages from control

273 Chromatin immunoprecipitation studies revealed that the GR and KLF

274 Reciprocal co-immunoprecipitation studies show that Megf10 and Notch1

275 Co-immunoprecipitation studies with epitope-tagged PP1c and

276 Using HDAC5 deletion mutants and co-immunoprecipitation studies, we showed that HDAC5 physic

277 ses using luciferase reporters and chromatin immunoprecipitation suggested that the -70 kb region ups

278 We confirmed by chromatin immunoprecipitation that P4 recruits PR to the CK5 promo

279 s with different epitope tags, we show by co-immunoprecipitation that this is true in vivo.

280 gated to adaptors, and after damage-specific immunoprecipitation, the adaptor-ligated oligonucleotide

281 cing of Rgs10 Furthermore, we used chromatin immunoprecipitation to demonstrate that H3 histones at t

282 nd reverse genetic approaches with chromatin immunoprecipitation to identify centromeres of the model

283 Western blotting, ELISA, and ChIP (chromatin immunoprecipitation) to characterize Pb-induced gene up-

284 and high throughput sequencing crosslinking immunoprecipitation) to evaluate simultaneous changes in

285 d higher voltage-gated potassium channel-IgG immunoprecipitation values (0.33nmol/l, range = 0.02-5.1

286 were determined in both sexes, and chromatin immunoprecipitation was used to determine transcription

287 ing, immunofluorescence cell staining and co-immunoprecipitation, we define a critical region at the

288 dual-luciferase reporter assay and Chromatin immunoprecipitation, we demonstrate there is a reciproca

289 well as targeted metabolomics and chromatin immunoprecipitation, were performed on the livers of the

290 hanistic insights were provided by chromatin immunoprecipitation, Western blot, and immunostaining.

291 esence of bona fide Abeta oligomers, whereas immunoprecipitation-Western blotting using high-detergen

292 These interactions were validated by immunoprecipitation/Western blotting, immunofluorescence

293 We developed a new technique that replaces immunoprecipitation with a simplified chromatin fragment

294 By using chromatin immunoprecipitation with CRISPR/Cas9 knockin of GFP fusi

295 Here, using co-immunoprecipitation with different channel domains, we f

296 Immunoprecipitation with menin or ubiquitin was used to

297 Using cell-based immunoprecipitation with plasma from cGVHD patients and

298 Here, by combining studies using chromatin immunoprecipitation with sequencing and RNA sequencing,

299 Immunoprecipitation with Sesn2 Ab revealed that cardiac

300 Immunoprecipitation with the RNA chaperone Hfq drafts an