ライフサイエンスコーパス: cell lysate

1 hieved for the detection of ERalpha in MCF-7 cell lysate.

2 of the kinase activity and inhibition in the cell lysate.

3 ntingtin aggregation in a cell model and its cell lysate.

4 e complex and slow with both whole cells and cell lysate.

5 ous concentrations in prostate cancer (PC-3) cell lysate.

6 complex biological samples such as serum and cell lysate.

7 the extraction of plasmid DNA from bacterial cell lysate.

8 ve standard deviations of up to 70% in crude cell lysate.

9 these ligands, even in samples as complex as cell lysate.

10 ies of pyrophosphopeptide in the presence of cell lysate.

11 ormation from nanogram quantities of protein cell lysate.

12 with standard protein mixtures and a complex cell lysate.

13 ross-linked protein-DNA complexes from yeast cell lysate.

14 with a concomitant retention of sGAG in the cell lysate.

15 is advantageous to measure miRNA in a crude cell lysate.

16 ide gel electrophoresis (PAGE) of the single-cell lysate.

17 s was performed in both a pure buffer and in cell lysate.

18 d analysis of picogram loadings of RAW 264.7 cell lysate.

19 nd dimers were successfully pulled down from cell lysate.

20 cterize full-length otoferlin from mammalian cell lysate.

21 espite the presence of growth media and Vero cell lysate.

22 h the protein(s) they react with in cells or cell lysate.

23 ed MALAT1 ENE+A RNA upon addition of HEK293T cell lysate.

24 mutant virus protein in the transfected BHK cell lysate.

25 strated with standard proteins and a complex cell lysate.

26 rks for complex mixtures of trypsin-digested cell lysate.

27 om a complex sample such as blood, serum, or cell lysate.

28 ectrometer for three proteins and an E. coli cell lysate.

29 at high concentrations as well as of a crude cell lysate.

30 es, to complex aggregates, as found in total cell lysates.

31 vity changes in hundreds of cysteines within cell lysates.

32 ipitated with IGF1 receptor (IGFR1) in whole-cell lysates.

33 mains that are unstructured when analyzed in cell lysates.

34 of NAAAR mutant gene libraries directly from cell lysates.

35 w separation of as little as 20 mug of total cell lysates.

36 little as 25 mug tryptic peptides from whole cell lysates.

37 extraction of phosphopeptides from the whole cell lysates.

38 PLC fractionation of Chlamydia-infected HeLa cell lysates.

39 ures and for protein-protein interactions in cell lysates.

40 single-molecule motility assays of mammalian cell lysates.

41 -fructofuranosidase activity in T. vaginalis cell lysates.

42 and can be recapitulated by eosinophil whole-cell lysates.

43 molecules and unpurified protein targets in cell lysates.

44 rove their binding to endogenous PDEdelta in cell lysates.

45 er to enrich for such methylated lysine from cell lysates.

46 ably Escherichia coli cell free extracts and cell lysates.

47 he specificity of an inhibitor of calpain in cell lysates.

48 able to profile molecular activities within cell lysates.

49 the LMM fractions of both tumor and nontumor cell lysates.

50 and inhibits the enzyme's lyase activity in cell lysates.

51 of tools for profiling enzyme activities in cell lysates.

52 ogram or sub-picogram levels per nanogram of cell lysates.

53 ) as an interaction partner of Arl8b from NK cell lysates.

54 g it more versatile than other methods using cell lysates.

55 rring amyloid-forming proteins directly from cell lysates.

56 porin A) in complex protein mixtures such as cell lysates.

57 identifying patterns of enzyme activities in cell lysates.

58 tivities of 3'-5' exonuclease and DNase I in cell lysates.

59 ns such as e.g., biotechnologically relevant cell lysates.

60 chia coli were quantitatively estimated from cell lysates.

61 tivity of ITPA in bacterial, yeast and human cell lysates.

62 of overexpressed proteins directly in crude cell lysates.

63 (CANC) nanotubes captured SUN1 and SUN2 from cell lysates.

64 molecules and unpurified protein targets in cell lysates.

65 relevant concentrations of ERBB2/neu/Her2 in cell lysates.

66 known endogenous protein binders in complex cell lysates.

67 eins added in crude Escherichia coli or 293T cell lysates.

68 tion of SPSB2-iNOS interaction in macrophage cell lysates.

69 7 bacteriophage and His6-GroEL directly from cell lysates.

70 t of hTS with one such peptidic inhibitor in cell lysates.

71 in the lysosomal fraction, but not in whole-cell lysates.

72 e for two different grades of bladder cancer cell lysates.

73 es individual caspases can cleave in complex cell lysates.

74 t of detection 0.3ng/mL (1.5pM) for ERBB2 in cell lysates.

75 ystem for triplicate analysis of a RAW 264.7 cell lysate; 2 +/- 1 and 7 +/- 2 protein groups were con

76 amine 500 mug of a human foreskin fibroblast cell lysate a total of 1,944 unique phosphopeptides from

77 n (out of 35 fractions) from a crude HEK 293 cell lysate, a total of 640 proteins were identified in

78 In CHO-IR cell lysates, a glutathione S-transferase chimera of the

79 is capable of detecting miRNA-143 in cancer cell lysates, allowing for the discrimination between th

80 rcial reagent that can easily generate crude cell lysates amenable to direct analysis by one-step RT-

81 on and increased ENaC abundance in the total cell lysate and at the cell surface.

82 Through cell lysate and cell assays, a promising lead candidate

83 is was achieved by coating MPs with human ES cell lysate and centrifugation of specific ratios of ES

84 s to induce coacervation in Escherichia coli cell lysate and follow gene expression under crowded and

85 ) in presence of luciferin substrate both in cell lysate and in living cells.

86 in vitro translation assay containing human cell lysate and purified target mRNA fused to a reporter

87 SOD, GR, and CAT activities in red blood cell lysate and saliva and MDA levels in plasma and sali

88 single-molecule pull-down (SiMPull) from HEK cell lysate and subunit counting in the plasma membrane

89 d secosterol A and B (Seco A and Seco B), in cell lysates and apical washes.

90 generation of protein alpha-thioesters from cell lysates and applied this strategy for the semisynth

91 of this iBody for the isolation of FAP from cell lysates and blood serum as well as for its detectio

92 ere also detected and semiquantified in both cell lysates and cell culture supernatants by Western bl

93 l, we tested varicella zoster virus-infected cell lysates and clinically isolated virus and found evi

94 We also found that HpGroES bound to TLR4 in cell lysates and colocalized with TLR4 on the cell membr

95 sed for quantitative PCR, while protein from cell lysates and conditioned media were used for immunob

96 RNA target mir-21 could be detected in crude cell lysates and detected by imaging in live cells.

97 AX-haptenated proteins were detected in cell lysates and extracellularly, either as soluble prot

98 and in vitro by immunoprecipitation in crude cell lysates and from fractions after gel filtration and

99 nation of the presence of SLT-1 from complex cell lysates and ham/juice samples based on the detectio

100 ctin glycoprotein ligand-1 (PSGL-1), both in cell lysates and in cell-free assays.

101 2-hydroxyglutarate is also observed, both in cell lysates and in vivo in orthotopic tumours.

102 nuclear antigen expression, respectively, in cell lysates and individual cells.

103 reduced the rate of c-di-GMP degradation in cell lysates and inhibited the activity of EAL-dependent

104 in CSF-1R-deficient U251 human glioblastoma cell lysates and inhibited the proliferation, clonogenic

105 rapid and sensitive detection of miRNAs from cell lysates and serum samples.

106 on by protein tyrosine phosphatases (PTP) in cell lysates and single cells and to investigate the eff

107 as biocatalysts was investigated using crude cell lysates and soluble protein fractions of Azospira o

108 Gag peptides were detectable in both cell lysates and supernatants in CD4+ T cells infected i

109 Virus from cell lysates and synthetic templates could be readily am

110 ines demonstrated that LH2 is present in the cell lysates and the conditioned media in a dimeric, act

111 nd coproporphyrin, based on HPLC analysis of cell lysates and the culture medium, as well as cell-fre

112 sed to quantify the extent of interaction in cell lysates and the equilibrium binding constant for th

113 n complex physiological environments such as cell lysates and to measure their individual activities

114 ed that CacyBP/SIP forms a homodimer in NB2a cell lysate, and biophysical methods demonstrated that C

115 sis of immunoprecipitation product from OSCC cell lysate, and in situ proximity ligation assays.

116 t antiserum was used for Western blotting of cell lysates, and gel slices corresponding to reactive b

117 from different proteomic setups (live cells, cell lysates, and immobilized affinity matrix), we found

118 Single-cell lysates are generated at defined time points and an

119 tion of NF-kappaB by C. trachomatis-infected cell lysates as a biomarker for the presence of PG fragm

120 EF1G were identified in fractionated human T-cell lysates as reverse transcription cofactors, as thei

121 lex, is broad in scope, and is applicable in cell lysates as well as to covalent inhibition/modulatio

122 nce-based quantification of this fraction in cell lysate at a time point of interest.

123 Reproducibility for metabolites in cell lysate averaged 9% RSD.

124 SPAG1 was present in human airway epithelial cell lysates but was not present in isolated axonemes, a

125 elivery of B. burgdorferi DNA, RNA, or whole-cell lysate, but not by lysate that had been treated wit

126 port on accurate miRNA quantitation in crude cell lysate by a CE-based hybridization assay termed dir

127 allel multiple GTP-bound GTPases in the same cell lysate by flow cytometry.

128 ermore, the alkyne-tagged glycoproteins from cell lysates can be directly detected with AzBOCEt in ge

129 , Kd values for unpurified proteins in crude cell lysates can be obtained without prior knowledge of

130 n vitro DISC is assembled in the presence of cell lysate, caspase-8 Y380 phosphorylation attenuates D

131 immunotherapy consisting of autologous tumor cell lysate combined with toll-like receptor ligands.

132 ied a high quantity of mRNA from crude yeast cell lysate compared to a phenol/chloroform extraction m

133 of soluble, assembled RuBisCO recovered from cell lysates compared with co-expression of RuBisCO with

134 In addition, cell lysates containing recombinant Shiga-like toxins ta

135 that pretreatment of cell free extracts and cell lysates containing Sav mutants with diamide affords

136 The cell lysate content was measured with scanning probe mic

137 pH-exposure of DM-DO in cell lysates corroborates such a pH-regulated mechanism,

138 Protein captured from a crude bacterial cell lysate could also be deuterated without the need fo

139 ltiple kinase activity profiling from single cell lysate could potentially allow us to study heteroge

140 cellular phenoloxidase activity (present in cell-lysates), demonstrates >98% reduction in activity a

141 fibronectin by peritoneal cell-derived mast cell lysates diminished GBS adherence.

142 or was applied to detect miRNA-215 from A549 cell lysate directly without complex sample treatment, a

143 rol the transport and handling of each 17-pL cell lysate during analysis.

144 de biosensor at fmol levels from aliquots of cell lysate equivalent to ~15,000 cells.

145 inked small molecules and a model library of cell lysates expressing SNAP-target fusions combined in

146 polyacrylamide gel electrophoresis of single cell lysates followed by an in-gel immunoassay.

147 PLA2 activity (MJ33 sensitive) in cell lysates following angiotensin II treatment of MPMVE

148 cent isotope abundance of (15)N-ammonia in a cell lysate for (15)N-isotope tracing studies.

149 Following cell lysis and sampling crude cell lysate for analysis, the substrate and the product

150 measuring inhibition of PKA activity in MCF7 cell lysates for a panel of nine compounds.

151 ntify changes in global activity profiles of cell lysates for a wide variety of enzymatic activities.

152 Tested at the level of whole cell lysates for glycoproteomic applications, three diff

153 ion of O-glycans from glycoproteins in whole cell lysates for mass spectrometric analysis.

154 hrome c (Cyt c) is an important biomarker in cell lysates for the early stage of apoptosis or antican

155 yl di- and tripeptides in Chlamydia-infected cell lysate fractions.

156 SY and 2D (13)C-(1)H HSQC-TOCSY spectra of a cell lysate from E. coli, which yields a substantial imp

157 Escherichia coli cell lysate with 100 mug of cell lysate from mouse, corresponding to expected relati

158 Furthermore, in vitro assays with crude cell lysate from PCE grown cells revealed dechlorination

159 is of GLD is based on GALC activity of total cell lysates from blood, which does not discriminate whe

160 n (VH H) libraries against antigens in total cell lysates from Chlamydomonas reinhardtii.

161 f differentially expressed proteins in whole cell lysates from E. coli.

162 l inflammation, ii) the capacity of necrotic cell lysates from HT29 cells or human IECs to induce hum

163 for the purpose of generating RT-qPCR-ready cell lysates from MDCK cells infected with influenza vir

164 ryosections, and the protein was detected in cell lysates from synovium obtained from OA patients.

165 When cell lysates from wild type-transfected MCF7 cells under

166 e corresponding antigen from a complex whole-cell lysate generates a change in refractive index in th

167 analysis (HILIC-RPLC) of S. cerevisiae whole cell lysate has been used to acquire retention informati

168 ements from crude cultured colorectal cancer cell lysates (HCT116) and biopsied tumor tissues.

169 -top-down MS analysis of Pyrococcus furiosus cell lysate identified 134 proteins and 291 proteoforms

170 By operating in cell lysates, IDUP preserves native post-translational m

171 n isoforms in immune-purified sample and raw cell lysate in 2 hours with sample volume requirements o

172 es; for example, it could be used to analyze cell lysate in drug response studies or pricks of blood

173 -1 protein is 0.0078mg/ml of T24 (Grade III) cell lysate in phosphate buffered saline, artificial uri

174 in our platform by both tracking fluorescent cell lysate in sealed microwells and with a human-mouse

175 report a simple platform for trapping single-cell lysates in sealed, picoliter microwells capable of

176 lows reproducible near-complete digestion of cells lysates in 1-5 min.

177 ns identified in a tryptic digest of E. coli cell lysate increased by 13% and 14%, respectively, alon

178 e receptor ligands and M. tuberculosis whole-cell lysate, increased M. tuberculosis replication, and

179 rine A with cyclophilin A protein in a yeast cell lysate is successfully detected and quantified usin

180 levels and modification states of kinases in cell lysates is described.

181 Dicer activity in crude cell lysates is increased in the presence of Ca(2+), mos

182 and RIG-I coimmunoprecipitation of infected cell lysates isolated immunostimulatory CCHFV RNA.

183 in each microwell; (iii) PAGE of each single-cell lysate; (iv) exposure of the gel to UV light to blo

184 probes capable of assessing CTB activity in cell lysates, living cells, and animal models of disease

185 rease in CEST image contrast was observed in cell lysates (mean +/- standard deviation, 0.52% +/- 0.0

186 consisted of invasively collecting samples (cells, lysates, media, etc.) from an OOC.

187 The bisacetate is more effective in cell lysates, more cytotoxic in prostate cancer cells th

188 Chemical treatments of M. tuberculosis whole-cell lysates (MtbWL) ruled out protein, nucleic acid, an

189 Western blot analysis of total cell lysate obtained from normal human mammary epithelia

190 was used to detect protein hydroperoxides in cell lysates obtained from macrophages exposed to visibl

191 for detection of solubilized p16 protein in cell lysates obtained from patients.

192 tudy, a microparticulate vaccine using whole cell lysate of a murine ovarian cancer cell line, ID8 wa

193 When used on data obtained from the cell lysate of an unexplored oncogenic cell line, it rev

194 m to rapidly identify SLT-1 from the complex cell lysate of E. coli O157:H7.

195 richment approach was initially applied to a cell lysate of the filamentous fungus Aspergillus niger.

196 components of PRC2, NuRD, and SIN3A from the cell lysate of the TNBC cell line SUM149.

197 Further, the measurement of cyt c release in cell lysates of cardiomyocytes using the GNP/PPy based i

198 Analysis of whole cell lysates of mouse brain, liver, red muscle fibers, a

199 ling lysine deacetylase (KDAC) activities in cell lysates of the CHRF megakaryocytic (Mk) cell line.

200 Cell lysates of the cyanobacterial mutants further funct

201 e responsible for degrading pGpG, we assayed cell lysates of WT and orn strains of P. aeruginosa PA14

202 9) developed titers of IgG response to whole-cell lysates of Y. pestis (YpL) and subunit LcrV similar

203 alization of the banding patterns from whole-cell lysates on SDS-PAGE gels, by direct staining and/or

204 tes peptide samples from protein mixtures of cell lysate or body fluid origin.

205 ates, have activity in the presence of human cell lysate or BSA, and catalyze dephosphorylation of a

206 However, selectivity was restored by crude cell lysate or purified G-actin, which joined PPP1R15-PP

207 d BALB/c mice were inoculated with sham HeLa cell lysate or rhinovirus.

208 d TSLP receptor-knockout mice with sham HeLa cell lysate or RV.

209 on and transformation results collected from cell lysates or fixed-cells conceal important dynamic in

210 Necrotic cell lysates potently induced HIF IL-6 and IL-8 producti

211 proteins based on 20 peptides from the 6 ng cell lysate prepared with our approach.

212 a linear dependence on the concentration of cell lysate present while specificity is demonstrated by

213 d band broadening, even when handling single-cell lysate protein concentrations in an open device.

214 eport here that HBc expressed in a mammalian cell lysate, rabbit reticulocyte lysate (RRL), was able

215 ting CYP119 mutants containing Ir(Me)-PIX in cell lysates, rather than as purified enzymes.

216 RNase treatment of cell lysates reduces Gzm cleavage of RNA binding protein

217 the quantitative chemical analysis of single-cell lysates remains difficult.

218 ide protein interactions in E. coli and HeLa cell lysates, respectively, identifying 1,158 and 3,301

219 Indeed, measurements in cell lysate reveal that the gate interconversion rate de

220 recipitation of viral proteins from infected cell lysates revealed association of UL84, UL44, and nuc

221 Western blot analysis of cell lysates revealed that APOE4 macrophages displayed e

222 were determined for miRNA samples in a crude cell lysate, RNA extract from the lysate, and a pure buf

223 in targets were discovered from a eukaryotic cell lysate (Saccharomyces cerevisiae).

224 teins from 9 injections from a single Jurkat cell lysate sample consisting of 400 ng of total protein

225 g agents such as neutral detergents found in cell lysate samples even at high concentrations.

226 Starting with tissue or cell lysate samples, all of the unmodified free thiols a

227 the quantitation of ErbB2 in human serum and cell lysates samples without any matrix effect.

228 at 37 degrees C incubation for 1-2 hours, in cell-lysate samples either freshly prepared or previousl

229 omplexes immunoprecipitated from RV-infected cell lysates show both forms of NSP2 are phosphorylated,

230 An in vitro assay on macrophage cell lysates showed complete inhibition of SPSB2-iNOS in

231 Assays of cell lysates showed that ATP-dependent 5-oxoprolinase ac

232 Moreover, the addition of purified RelE to cell lysates shows promise as a method for generating ri

233 of effectively enriching SLT-1B from complex cell lysates simply by pipetting 20 muL of the sample in

234 l samples was assessed by testing samples of cell lysate solutions obtained from human astrocytoma (g

235 binding domains (LBDs) can be recruited from cell lysates specifically onto their target phospholipid

236 r the extraction of DNA from crude bacterial cell lysate spiked with 1 pg mL(-1) template DNA without

237 din-Sepharose beads to GL-biot-treated DU145 cell lysates, STAT3 was isolated and identified as a tar

238 t predominately precipitates with Hsp70 from cell lysates, suggesting a role for SGTA in early, Hsp70

239 e specific activity of M. tuberculosis whole-cell lysates, suggesting that a polysaccharide was requi

240 t of affinity-modulating adaptor proteins in cell lysates that would be absent in ligand screening or

241 uted by 100-fold in a trypsin-digested whole cell lysate, the O-GlcNAcylated peptide remains detectab

242 on with an immunoassay-based analysis of the cell lysate, the platform allowed the selective and sens

243 ollowing PIL-based SPME of DNA from a dilute cell lysate, the qPCR amplification efficiency was deter

244 In A431 cell lysates, the reporter was a poor substrate for pept

245 onality) to a tryptic digest of whole Jurkat cell lysate to estimate the depth of proteome coverage a

246 thase, was purified in only ten minutes from cell lysate to near homogeneity (>90 %).

247 A bisacetate analogue is converted in cell lysates to 3a.

248 Six proteins were purified from complex cell lysates to average homogeneities of 76 %.

249 cted hydrogen-deuterium exchange of quenched cell lysates to measure individual opening free energies

250 ty purified PI4KIIalpha from isotope-labeled cell lysates to quantitatively identify interactors.

251 ible to purify phytase simply by heating the cell lysate, to drive aggregation of non-cyclized protei

252 g a multistep enrichment strategy from whole cell lysate, to evaluate their abilities to enrich for d

253 ged protein complexes from minute volumes of cell lysates under close to physiological conditions and

254 to isolate interacting proteins from E. coli cell lysates under non-denaturing conditions.

255 dividual SOS molecules are captured from raw cell lysate using Ras-functionalized supported membrane

256 s and that these peptides can be detected in cell lysates using a bottom-up proteomic approach.

257 ferase activities of purified proteins or in cell lysates using a mass-differentiated carbohydrate li

258 P)-235, and Ser(P)-396/404) were measured in cell lysates using AlphaScreen assays.

259 olute quantitation of endogenous proteins in cell lysates using an automated capillary immunoassay sy

260 ) can be specifically pulled from K562 human cell lysates using beads decorated with phosphorylated g

261 s can be assessed by fractionating tissue or cell lysates using differential ultracentrifugation thro

262 nhibition by small molecules and activity in cell lysates using parallel DNA sequencing or quantitati

263 ions (1 x 10(2) CFU/ml) was detected in FCDI cell lysates using real-time PCR with greater consistenc

264 nd quantitation of carbonyl metabolites from cell lysate was accomplished using a carbonyl-reactive f

265 S analysis (SCX-RPLC) of S. cerevisiae whole cell lysate was used to generate a retention dataset of

266 When a B16F10 melanoma cell lysate was used to load DCs with tumor antigens dur

267 resis to grossly enrich GSK-3beta from whole cell lysate, we discover by MRM-MS a novel O-GlcNAcylate

268 e-adapted sedimentation velocity analysis of cell lysates, we collated a multidimensional view of Htt

269 arget 6 and Mycobacterium tuberculosis whole-cell lysate were associated with reduced bacillary burde

270 Cell lysates were analyzed by immunoprecipitation with a

271 or this purpose, tryptic peptides from whole cell lysates were analyzed by sheathless CE-ESI-MS/MS an

272 ene clone H3 (betaIGH3) mRNA expression from cell lysates were analyzed.

273 Cell lysates were prepared and reacted with glutathione-

274 Cell lysates were processed for IGFBP-3 ELISA analyses a

275 MiR-214 levels in exosomes but not in cell lysates were reduced by pretreatment of the cells w

276 could also be detected in dimeric form when cell lysates were subjected to SDS-PAGE under non-reduci

277 eriments using retinal or transfected HEK293 cell lysates were used to investigate the association be

278 ge tubes, a suitable method for studies with cell lysates when enzyme activity was moderate; and (iii

279 ed affinity probes report on KAT activity in cell lysates, where KATs exist as multiprotein complexes

280 In contrast to the whole CHO cell lysate which contained a variety of fatty acids, ca

281 These assays are performed on cell lysates, which circumvents the labor-intensive step

282 o the quantitative determination of Cyt c in cell lysates, which opens a new avenue to early diagnost

283 fied a subset of HDAC8 substrates from human cell lysates, which were further validated for catalytic

284 mixing 5, 10, 15 and 20 mug Escherichia coli cell lysate with 100 mug of cell lysate from mouse, corr

285 Separation of a cell lysate with a 60 min gradient showed extremely high

286 ferase added in the Escherichia coli or 293T cell lysate with better staining sensitivity than conven

287 and purification of DNA from crude bacterial cell lysate with subsequent quantification by real-time

288 ctivated as verified by cotreatment of HepG2 cell lysates with (2E)-hexadecenal and the acyl-CoA synt

289 thylated proteins are enriched by incubating cell lysates with 3xMBT, or with the binding-null D355N

290 rated using proteome-wide reactions of HT-29 cell lysates with a model probe of threonine beta-lacton

291 Moreover, incubations of cell lysates with deuterated (2E)-hexadecenal revealed t

292 mmunoprecipitation assay of mouse ameloblast cell lysates with either ameloblastin or Psma3 antibody

293 hibited dephosphorylation of the reporter in cell lysates with IC50 values of 470 nM, 35 muM, and 100

294 formation can be performed in blood serum or cell lysates with minimal interference from biomolecules

295 sed the phosphorylation status of Mga in GAS cell lysates with Phos-tag gels.

296 large number of MTs (>50) from human cancer cell lysates with remarkable specificity over other clas

297 ns, Western blotting of SHFV-infected, MA104 cell lysates with SHFV nsp1 protein-specific antibodies

298 attomoles of glycoproteins of interest from cell lysates, with sensitivity several orders of magnitu

299 tone inhibited STAT3 binding to DNA in DU145 cell lysates without affecting phosphorylation status of

300 of a low-abundance transcription factor from cell lysates without need for isolation or enrichment.