ライフサイエンスコーパス: pulldown

1 vels in a Dicer null cell line, and (3) Ago2 pulldown.

2 ined four proteins on an anti-FABP1 antibody pulldown.

3 CSNAP (Chemical Similarity Network Analysis Pulldown), a new computational target identification met

4 Here we miniaturize the concept of affinity pulldown, a gold-standard in vitro PPI interrogation tec

5 ed activation of GEF-H1 and RhoA detected in pulldown activation assays.

6 Thus, our MBD pulldown alignment model can improve methylation predict

7 Glutathione S-transferase (GST) affinity pulldowns also suggest that p18 and Gag interact.

8 However, both structural and pulldown analyses have suggested that EspG cannot intera

9 ransfer (FRET) and glutathione S-transferase pulldown analyses identified Akt1 pleckstrin homology do

10 Immunoprecipitation and pulldown analyses revealed that Plk3 physically interact

11 e EGFR by coimmunoprecipitation and affinity pulldown analyses, and the primarily trans-Golgi network

12 Here, using mutagenesis-based kinetic and pulldown analyses, we show that Noonan syndrome Ras muta

13 Accordingly, pulldown analysis and fluorescent FKBP12 binding studies

14 Immuno-pulldown analysis from wild-type (WT) mouse tissue showe

15 A pulldown analysis of eIF3 subunits associated with the H

16 Pulldown analysis revealed that Cdh1, but not Cdc20, was

17 Pulldown analysis revealed that Plk1 physically interact

18 e globular regions of C1q as demonstrated by pulldown and cell surface co-localization experiments.

19 By oligonucleotide pulldown and chromatin immunoprecipitation assays, we fo

20 The interaction was confirmed by in vitro pulldown and co-immunoprecipitation assays and was shown

21 ms a stable complex with DAT in vivo via GST pulldown and co-immunoprecipitation assays.

22 merizations of these three NHERF proteins by pulldown and co-immunoprecipitation assays.

23 Pulldown and co-immunoprecipitation experiments identifi

24 P1 interaction was confirmed by both peptide pulldown and coimmunoprecipitation assays, which also de

25 GST pulldown and coimmunoprecipitation studies reveal that R

26 Using in vitro pulldown and competition assays, we demonstrate that thi

27 equences was demonstrated by oligonucleotide pulldown and fluorescence polarization.

28 is an interacting partner of IRSp53 through pulldown and Forster resonance energy transfer analysis,

29 We show by mutagenesis, pulldown and hydrogen/deuterium exchange mass spectromet

30 o glutathione S-transferase (GST) E-cadherin pulldown and immunoblot analysis to assess levels of unc

31 man cell lines, fluorescence microscopy, and pulldown and immunoblotting assays, we show that alpha-d

32 SA-agarose pulldown and immunoblotting for IRF5 were used to determ

33 Pulldown and immunofluorescence binding assays and surfa

34 Nanog directly binds the FAK protein by pulldown and immunoprecipitation assays, and proteins co

35 In protein pulldown and immunoprecipitation experiments, binding of

36 olecular mechanisms were investigated by RNA pulldown and immunoprecipitation, mass spectrometry, mic

37 racts with ERK1/2 by using both in vitro GST pulldown and in vivo co-immunoprecipitation assays.

38 GST pulldown and indirect enzyme-linked immunosorbent assays

39 bination of GFP nanotrap association assays, pulldown and integrin-binding assays, and live-cell imag

40 Affinity pulldown and kinase profiling studies implicate Erb3 bin

41 is simple, reusable, and also applicable to pulldown and kinetic activity/binding assays.

42 By oligonucleotide pulldown and mass spectrometry discovery approaches, we

43 Using peptide pulldown and mass spectrometry, we identified angiomotin

44 target of Semapimod using ATP-desthiobiotin pulldown and mass spectroscopy.

45 , coimmunoprecipitation and HDAC assays, and pulldown and NMR experiments, we show that HDAC1/2 deace

46 d PAT1 was further confirmed by in vitro GST pulldown and overlay assays and in intact neutrophils an

47 We have used pulldown and peptide array overlay assays to study inter

48 Vav3-Cdc37 interaction was confirmed by GST pulldown and, for native proteins, by co-immunoprecipita

49 GST-based pulldowns and coimmunoprecipitation experiments demonstr

50 We demonstrate in this paper using GST pulldowns and coimmunoprecipitation studies that SAP con

51 RNA pulldowns and costainings show that MyoD mRNA interacts

52 Pulldowns and isothermal titration calorimetry revealed

53 Further analysis using pulldowns and size-exclusion chromatography underscored

54 MORF proteins by yeast two-hybrid, in vitro pulldown, and bimolecular fluorescence complementation a

55 Ai, in situ epitope tagging of proteins, GST pulldown, and coimmunoprecipitation assays, and immunofl

56 FAK could be shown by mammalian two-hybrid, pulldown, and far Western studies.

57 Here, using various enzymatic, pulldown, and immunoprecipitation assays, we describe si

58 tography, Forster resonance energy transfer, pulldown, and in vitro GEF assays to demonstrate that re

59 in staining, delayed competition in affinity pulldown, and inhibition of TNF biogenesis after washout

60 he inclusion of any estimate of SssI Control pulldown, and is comparable to - and in some cases bette

61 human and murine cells; immunoprecipitation, pulldown, and surface plasmon resonance assays; and immu

62 Immunohistochemical colocalization, GST pulldown, and surface plasmon resonance studies revealed

63 g, peptide-N-glycosidase F treatment, lectin pulldowns, and exoglycosidase treatment, we have now inv

64 ed Hspb1 mRNA in wild-type lens lysate TDRD7-pulldowns, and single-molecule RNA imaging showed co-loc

65 onuclease-deficient Cas9-based gene promoter pulldown approach coupled with mass spectrometry, we fou

66 Using a novel RNA pulldown approach that utilized endogenous S1-tagged PIN

67 We then used a DNA pulldown approach to discover that eptA transcription is

68 We used a biotinylated RNA pulldown approach to isolate host factors binding to the

69 Using a directed RNA pulldown approach, we identified two components of this

70 Similarly, results from CBX4-BioTAP protein pulldowns are consistent with reports of a diversity of

71 rabidopsis and Nicotiana benthamiana using a pulldown assay and fluorescence resonance energy transfe

72 egion of AKAP79 was able to bind PP1 by both pulldown assay and surface plasmon resonance.

73 interaction by site-directed mutagenesis and pulldown assay and thereby confirm that the major bindin

74 s work establishes the single-molecule lipid pulldown assay as a simple and highly sensitive approach

75 A protein pulldown assay coupled with mass spectrometry identified

76 A RAS-binding domain pulldown assay indicated that RIT1 A57G and Y89H were hi

77 Pulldown assay of GST-KOPR-C-tail with HA-GEC1 or HA-GAB

78 to embryonic organ explants, with a microRNA pulldown assay that allows direct identification of micr

79 To address this, we used an in vitro pulldown assay to define a series of five arginine resid

80 phila melanogaster and performed an unbiased pulldown assay to identify all possible interactions, re

81 A luciferase reporter assay and a pulldown assay using biotinylated INS-class I VNTR probe

82 V envelope glycoproteins were also used in a pulldown assay with beads coated with heparin, a close H

83 s and analyzed Rab5 binding with an in vitro pulldown assay with GST-Rab5(GTP) Of the 35 p110beta hel

84 otein-RNA reconstitution and a stringent RNA pulldown assay with human choriocarcinoma (JAR) cells, w

85 ctivity enzyme-linked immunosorbent assay, a pulldown assay, and immunostaining with a monoclonal ant

86 ipt in human T cells and found, using biotin pulldown assay, that HuR specifically interacts with its

87 In a pulldown assay, the His-tagged Myb1 interacted with a GS

88 d to form a stable complex with SpoIVFB in a pulldown assay.

89 led-coil domain of MuRF1 was demonstrated by pulldown assay.

90 f apoE, as determined by an in vitro heparin pulldown assay.

91 to 549, by a glutathione S-transferase (GST) pulldown assay.

92 s by confocal microscopy and in an in vitro "pulldown" assay.

93 In vitro pulldown assays also indicate that DinB(C66A) binds RecA

94 The pulldown assays also indicated the presence of Cox16p in

95 Furthermore, our results from both GST pulldown assays and analytical ultracentrifugation show

96 een aldolase and SUR was confirmed using GST pulldown assays and coimmunoprecipitation assays.

97 Using heme-affinity pulldown assays and proteomics of lysates from primary c

98 70-binding site in SOD2, we used a series of pulldown assays and showed that hsp70 binds to the amino

99 DM2 required for p21(Waf1) degradation using pulldown assays and Western blotting and then examined t

100 Complementary to this, we applied pulldown assays as well as microscale thermophoresis as

101 ation analysis, immunoprecipitation, and GST pulldown assays based on the theoretical predictions rev

102 We used L-selectin cytoplasmic tail peptide pulldown assays combined with high sensitivity liquid ch

103 Using pulldown assays combined with mass spectrometry analysis

104 Co-immunoprecipitation and pulldown assays confirmed PKC and beta-catenin as bindin

105 Pulldown assays confirmed that the binding between the p

106 Pulldown assays confirmed the presence of newly translat

107 In vitro pulldown assays confirmed this interaction, which was fo

108 Co-immunoprecipitation and pulldown assays coupled with site-directed mutagenesis d

109 GST pulldown assays demonstrate that the dimerization domain

110 Pulldown assays demonstrated interaction between betaCaM

111 erminal kinase domain combined with in vitro pulldown assays demonstrated that eriodictyol, a flavano

112 Pak-CRIB pulldown assays demonstrated that Norbin promotes the P-

113 RNA pulldown assays demonstrated that SRSF3 binds to an alte

114 Glutathione S-transferase (GST) pulldown assays demonstrated that the hnRNP H NLS intera

115 Two-hybrid and pulldown assays demonstrated that UL20, but no other HSV

116 GST pulldown assays demonstrated that vIRF1 interacts with U

117 roteins within platelets and confirmation by pulldown assays followed by immunoblotting, we identifie

118 Pulldown assays from Arabidopsis thaliana tissue culture

119 trometry and glutathione S-transferase (GST) pulldown assays identified integrin alpha5 as a novel Sc

120 GST pulldown assays in yeast lysates demonstrated physical i

121 , isothermal titration calorimetry data, and pulldown assays indicated that CaM-N and CaM-C both can

122 Structural results and pulldown assays indicated that L3 renders an in-built ge

123 In this study, glutathione S-transferase pulldown assays indicated that residues 1 to 68 of UL84

124 Pulldown assays of a Orai1-CMBD(W76E) mutant, gel filtra

125 Immunoprecipitation and pulldown assays of purified proteins demonstrated a dire

126 Finally, pulldown assays reveal a bipartite physical interaction

127 Co-immunopurification and pulldown assays reveal that P2X4 receptors complex with

128 Coimmunoprecipitation and in vitro pulldown assays reveal that phosphorylation of MyoGEF at

129 Pulldown assays revealed an interaction between NS5A and

130 Glutathione S-transferase pulldown assays revealed binding of CFTR to alpha-AP-2 (

131 Pulldown assays revealed that chimeric Galpha(13-i2)QL i

132 Rho pulldown assays revealed that Cryptococcus induces activ

133 pitation and glutathione S-transferase (GST) pulldown assays revealed that GBP1 interacted with the N

134 ctivity in RIalpha-knockdown cells, and cAMP pulldown assays revealed that P-REX1 preferentially inte

135 Pulldown assays revealed that Rab5-GTP levels are decrea

136 Yeast two-hybrid and direct pulldown assays revealed that the N-terminal domain of t

137 Results from pulldown assays show that ARF6 exchanges GDP for GTP in

138 r hemin exporter, results with hemin-agarose pulldown assays showed that Abc3 binds to hemin.

139 Pulldown assays showed that NS2 forms complexes with bot

140 by absorbance spectroscopy and hemin-agarose pulldown assays showed that Shu1 interacts with hemin, w

141 In vitro and in vivo pulldown assays showed that the carboxyl-terminal region

142 RNA pulldown assays showed that UL84 interacted with IRS1 mR

143 In vitro translation and pulldown assays suggest direct interaction between BCL10

144 Here, we show by yeast two-hybrid and pulldown assays that SpoVID also interacts directly with

145 selected biochemical pathways; (c) affinity pulldown assays that, in some cases, confirm and even ex

146 al mRNA-binding proteins identified from RNA pulldown assays to determine which of these exhibit bona

147 Here, we used biolayer interferometry and pulldown assays to identify regions of RAG1 necessary fo

148 Using G protein activity and in vitro pulldown assays we demonstrate that G alpha(i3) is a bet

149 depending on its CTD phosphorylation state, pulldown assays were performed using the CTD of the duck

150 lectrophoretic mobility shift assays and DNA pulldown assays with ChIP-PCR confirmed that MZF1 binds

151 However, our enzyme pulldown assays with different polymeric substrates sugg

152 o-immunoprecipitation, two-hybrid assay, and pulldown assays with expressed proteins.

153 For the active residues, we performed pulldown assays with membrane-impermeable 2-aminoethyl m

154 Pulldown assays with purified GST-l-PGDS and His(6)-Rab4

155 say that combines principles of conventional pulldown assays with single-molecule fluorescence micros

156 ults from flow cytometry, live-cell imaging, pulldown assays, and genetically-modified cell lines sup

157 Here, using size-exclusion chromatography, pulldown assays, and small angle x-ray scattering, we sh

158 brid mating and co-transformation protocols, pulldown assays, and surface plasmon resonance analysis.

159 In pulldown assays, CR binding to fusion proteins containin

160 biophysical methods, including heterocomplex pulldown assays, far-UV CD spectroscopy, the thioflavin

161 ombination of kindlin knockdown, biochemical pulldown assays, fluorescence microscopy, fluorescence r

162 oplasmic capping complex was demonstrated by pulldown assays, gel filtration and proximity-dependent

163 Using affinity pulldown assays, isothermal titration calorimetry, and t

164 As shown with affinity pulldown assays, PrgJ and the K471E mutant protein inter

165 In immunoprecipitation and pulldown assays, ShcA, via its SH2 domain, was associate

166 GST-VCP/p97 bound purified PP2A in pulldown assays, showing direct protein-protein interact

167 acted with the helicase domain of BKV Tag in pulldown assays, suggesting that NFI helps recruit Tag t

168 Using pulldown assays, surface plasmon resonance, and isotherm

169 By GST pulldown assays, the interaction domains between HMG2L1

170 In pulldown assays, the rank order of AnkG binding strength

171 g luciferase p-miR-Report constructs and RNA pulldown assays, we confirmed that miR-511 bound directl

172 Using pulldown assays, we demonstrate that SIRT1-Delta2/9 bind

173 By pulldown assays, we discovered that in addition to the p

174 Furthermore, using pulldown assays, we discovered that Sam68 is a possible

175 ce energy transfer experiments, and in vitro pulldown assays, we have now identified the key residues

176 Using the human Cad11 cytoplasmic domain in pulldown assays, we identified human angiomotin (Amot),

177 pitation (co-IP), mass spectrometry, and GST pulldown assays, we identified poly(ADP-ribose) polymera

178 re, using an array of immunofluorescence and pulldown assays, we report that expression of active or

179 assays, and glutathione S-transferase (GST) pulldown assays, we show that NR2A subunits interact dir

180 We next performed pulldown assays, with GGGGCC5, in conjunction with mass

181 al 44 amino acids of PDZD11, as shown by GST-pulldown assays.

182 h phosphatase abolishes their association in pulldown assays.

183 and in vitro glutathione S-transferase (GST) pulldown assays.

184 otein complex immunoprecipitation and biotin pulldown assays.

185 ), as shown by yeast two-hybrid and in vitro pulldown assays.

186 by using RNA immunoprecipitation and biotin pulldown assays.

187 cence, flow cytometry, real-time RT-PCR, and pulldown assays.

188 co-immunoprecipitation and in vitro protein pulldown assays.

189 d as the 14-3-3 binding region by GST-14-3-3 pulldown assays.

190 d the TM 4,5-loop was demonstrated using GST pulldown assays.

191 1 for binding to both PP2Acalpha isoforms in pulldown assays.

192 th E2 and interacted only weakly with NS3 in pulldown assays.

193 n protein (amino acids 475-589) on liposomal pulldown assays.

194 ently confirmed by glutathione S-transferase pulldown assays.

195 elope biosynthetic enzymes such as Ag85A via pulldown assays.

196 The interaction was confirmed by GST pulldown, blot overlay, and co-immunoprecipitation assay

197 ng endosome compartments were seen following pulldown by immunoaffinity chromatography with Rab-speci

198 n was confirmed by glutathione S-transferase pulldown, coimmunoprecipitation, and laser confocal micr

199 s (colocalization, glutathione S-transferase pulldown, coimmunoprecipitation, yeast two-hybrid, gel s

200 this stem-loop region using an RNA affinity pulldown-coupled mass spectrometry approach and identifi

201 in this study, BayMeth used with our modeled pulldown coverage performs better than BayMeth run witho

202 ed data in predicting methylation state on a pulldown data set with matching WGBS estimates.

203 In both internal and external MBD pulldown data sets tested in this study, BayMeth used wi

204 T84D enhances the ability of origin ssDNA to pulldown Dpb11, and Sld2 binding to origin ssDNA may be

205 reated samples, from which we also find that pulldown efficiency sharply increases for DNA fragments

206 found, although the corresponding biases in pulldown efficiency were all <5%.

207 equence specificity of MBD2-DNA binding in a pulldown experiment revealing three potential biases in

208 AGO-RNA pulldown experiment showed enrichment of AR, VEGFA and m

209 yl-CpG/MBD2 binding in the context of an MBD pulldown experiment, we build a model of expected MBD pu

210 third protein in yeast three-hybrid assays, pulldown experiments (luminescence-based mammalian inter

211 Pulldown experiments also indicated that all four core p

212 Pulldown experiments and chemical shift perturbation ana

213 According to pulldown experiments and in vitro binding assays, Cspalp

214 However, the target was identified based on pulldown experiments and in vitro binding data, without

215 Pulldown experiments and NMR spectroscopy revealed that

216 Pulldown experiments confirmed these results, as HMGB1 w

217 Yeast two-hybrid, co-immunoprecipitation and pulldown experiments demonstrate Piasy and Pias1 interac

218 Single-molecule pulldown experiments demonstrate that each molecule of O

219 Finally, pulldown experiments demonstrated that miR-125b physical

220 By RNA pulldown experiments followed by MALDI/TOF-MS analysis,

221 Pulldown experiments from adult parasite culture medium

222 Co-immunoprecipitation and pulldown experiments in livers of mice and in vitro usin

223 ct interaction between Med19 and Med1 by GST pulldown experiments indicating privileged contacts betw

224 Co-immunoprecipitation and GST pulldown experiments provided evidence that EPLIN intera

225 RNA pulldown experiments reveal that PTBP1 interacts with hT

226 Glutathione S-transferase pulldown experiments revealed a direct interaction betwe

227 Mutagenesis and pulldown experiments revealed multiple Hsp70-binding sit

228 Pulldown experiments revealed that it is not stably asso

229 Protein microarray and pulldown experiments revealed that this is indeed the ca

230 and glutathione S-transferase fusion protein pulldown experiments show that tyrosol-phosphorylated Er

231 Coimmunoprecipitation and biotin pulldown experiments showed that GR associates with CCL2

232 Pulldown experiments showed that the hsp90-iNOS complex

233 HCV pulldown experiments showed that this phenomenon was cau

234 ological measurements in Xenopus oocytes and pulldown experiments to analyze the direct interaction b

235 Pulldown experiments using affinity-tagged Spx showed th

236 Pulldown experiments using extracts of B. subtilis cells

237 his is a direct interaction, demonstrated by pulldown experiments using purified proteins.

238 affinity for matrix compared with p6 in GST-pulldown experiments was higher for ALIX than for TSG101

239 unoprecipitation and AQP0 C-terminal peptide pulldown experiments were used to confirm the protein-pr

240 ial ligand lipopolysaccharide and subsequent pulldown experiments with biotin-avidin affinity chromat

241 We performed pulldown experiments with biotinylated thymosin beta-4 (

242 Pulldown experiments with K. stuttgartiensis cell-free e

243 eins interacting with GlyRbeta, we performed pulldown experiments with rat brain extracts using a glu

244 wo proteins using co-immunoprecipitation and pulldown experiments with truncated or mutant Drosophila

245 trast, results from kinetic studies, heparin pulldown experiments, and inhibition experiments with an

246 analysis, immunoprecipitations, mutagenesis, pulldown experiments, and peptide arrays constrained PP1

247 (v) According to 20 S proteasome pulldown experiments, Hsp60 is physically associated wit

248 ected mutagenesis, glutathione S-transferase pulldown experiments, immunofluorescence, molecular mode

249 In pulldown experiments, PC1 bound to Galpha(12), but not t

250 ts in HEK-293 cells and Xenopus oocytes with pulldown experiments, we analyzed the direct interaction

251 -tagged in vivo and used as bait in separate pulldown experiments.

252 unoprecipitation and AQP0 C-terminal peptide pulldown experiments.

253 embled the GAP complex in label transfer and pulldown experiments.

254 to monitor Myo1c phosphorylation, along with pulldown, fluorescence binding, and additional biochemic

255 Affinity pulldown followed by mass spectrometry revealed that cir

256 PAR-resin pulldown, followed by proteomic analysis, demonstrated h

257 le length regulators were identified in EML1 pulldowns from embryonic brain extracts.

258 SMILR pulldowns further revealed its potential molecular mecha

259 This is confirmed by comparing input versus pulldown high-throughput sequencing data on M.SssI-treat

260 o anti-ubiquitin were seen in the optineurin pulldown, indicating that optineurin was ubiquitinated.

261 shion, SDCP-MS (SNP-specific DNA competition pulldown-mass spectrometry) to identify fSNP-bound prote

262 pled to a green fluorescent protein-nanotrap pulldown methodology and liquid chromatography-tandem ma

263 Cq-IGFBP) protein was produced and, using a "pulldown" methodology, was shown to specifically interac

264 Protein pulldown, molecular docking, molecular dynamics simulati

265 nterrogation technique, to perform nanoscale pulldowns (NanoSPDs) within living cells.

266 re, we used immunoprecipitation and affinity pulldown of ectopically expressed p30 coupled with mass

267 ircPVT1, only let-7 was found enriched after pulldown of endogenous CircPVT1, suggesting that CircPVT

268 ic peptides, as well as CaM-agarose affinity pulldown of full-length recombinant BdALMT12, we confirm

269 ts an initial slow slip followed by a sudden pulldown of the Philippine Sea slab so rapid that it cau

270 Using affinity pulldowns of Strep-tagged UAPs from Arabidopsis and rice

271 au interaction cluster that contained 33 Tau pulldown proteins.

272 experiment, we build a model of expected MBD pulldown reads as drawn from SssI-treated DNA.

273 ed these findings through deep sequencing of pulldown regions and whole-genome sequencing of independ

274 biological approaches, including active RAS pulldown, reporter and Comet assays, small interfering R

275 Moreover, affinity pulldowns show that p18 and the CTR interact.

276 GST pulldown showed that TAT-SNAP-23 bound to the combinatio

277 We use the single-molecule pulldown (SiMPull) assay that combines principles of con

278 By means of single-molecule pulldown (SiMPull), we determined a TAP/tapasin ratio of

279 Using poly(A) pulldown stranded RNA-seq and a 3' end transcript counti

280 Here, we use a novel RNA pulldown strategy coupled with mass spectrometry to iden

281 munoprecipitation and biotin-labeled miR-665 pulldown studies identified Kat6a as another potential t

282 FRET and surface pulldown studies in cell lines revealed that PKC activat

283 Vesicle pulldown studies showed that acidic phospholipids recrui

284 Using colocalization and pulldown studies we further document a noggin-insensitiv

285 t signaling that interacts with the VDR, GST pulldown studies were performed.

286 ble proteins were studied by a precipitation pulldown technique.

287 ly to purified 14-3-3zeta as demonstrated by pulldown techniques.

288 ed animals demonstrated stronger acute viral pulldown than controls, but a trend for higher acute vir

289 , we have utilized glutathione S-transferase pulldowns, two-hybrid analysis, and NMR to demonstrate t

290 is interaction was confirmed by a reciprocal pulldown using FLAG-tagged Ycf54 as bait.

291 Protein pulldown using Methyl-CpG binding domain (MBD) proteins

292 Biotin-RNA pulldown, UV-crosslinking and gel shift experiments indi

293 lly induced dimerization and single-molecule pulldown, we revealed that increasing the proximity of a

294 Using pulldowns, we here identify teneurins, type II transmemb

295 By using glutathione S-transferase (GST) pulldowns, we identified an essential role of lysine 343

296 density gradient centrifugation and antibody pulldowns, we show that all six A subunits are associate

297 Using TurboID proximity labeling and pulldowns, we show that LUZP1 associates with factors li

298 Protein pulldowns were used to identify Fam65b-interacting prote

299 proteins and AIDP-Wb (allele-imbalanced DNA pulldown-Western blot) to detect allele-specific protein

300 ots, reporter assays, biotin-tagged promoter pulldown with proteomics, and loss-of-function studies.