ライフサイエンスコーパス: lysate

1 lowing stimulation with an EBV-infected cell lysate.

2 uantification of unlabeled compounds in cell lysate.

3 0 phosphopeptides from 100 mug of MCF-7 cell lysate.

4 d perform western blotting on each resultant lysate.

5 ivated by a Mycobacterium tuberculosis (Mtb) lysate.

6 cy (RO) for a covalent binding drug in blood lysate.

7 rification of nucleic acids from the sampled lysate.

8 fectively used with purified protein or cell lysate.

9 d for the detection of ERalpha in MCF-7 cell lysate.

10 dvantageous to measure miRNA in a crude cell lysate.

11 de novo sequencing using whole cell E. coli lysate.

12 andard deviations of up to 70% in crude cell lysate.

13 ough on-chip electrical sensing of bacterial lysate.

14 en when dispersed in BSA or Escherichia coli lysate.

15 minant AEBSA target in diluted serum or cell lysate.

16 re protective compared to an uninfected cell lysate.

17 purity of >90% mitochondrial proteins in the lysate.

18 ered saline (PBS) and spiked in E. coli cell lysate.

19 of the total protein from breast cancer cell lysates.

20 demonstrated in food samples using crude DNA lysates.

21 rified esterases in bacterial and human cell lysates.

22 ment showed accumulation of LC3B II in heart lysates.

23 ing either protein standards or complex cell lysates.

24 ll as profiling glycosylase activity in cell lysates.

25 either FLAG or DYKD epitopes from crude cell lysates.

26 munoprecipitated from Schwann cell and nerve lysates.

27 es endogenous KCTD proteins from mouse brain lysates.

28 ins that bind to rRNA G-quadruplexes in cell lysates.

29 mounts of ADP-ribosylated peptides from cell lysates.

30 tivity of caspase-7 in Escherichia coli cell lysates.

31 ted and thioesterified forms of Ub from cell lysates.

32 m and function were also evaluated in tissue lysates.

33 vivo with parasite schizont and erythrocyte lysates.

34 y broad PcG domains in wildtype whole embryo lysates.

35 kines were measured in plasma and neutrophil lysates.

36 avage of PrP(C) is observed in mouse retinal lysates.

37 detection 0.3ng/mL (1.5pM) for ERBB2 in cell lysates.

38 -purified with PfMyoA isolated from parasite lysates.

39 tryptase were measured in plasma and biopsy lysates.

40 ies recognized native Siglec-E within spleen lysates.

41 exposed to P. falciprum infected erythrocyte lysates.

42 to profile molecular activities within cell lysates.

43 ly active Fic(E247G) mutant in Drosophila S2 lysates.

44 y of ITPA in bacterial, yeast and human cell lysates.

45 roteins, protein complexes or clarified cell lysates.

46 and CXCL2 were reduced in Il1a(-/-) oviduct lysates.

47 e the endogenous protein from mammalian cell lysates.

48 ltiple Ral-effector interactions in cellular lysates.

49 )-dependent desuccinylation activity in cell lysates.

50 culture media, but increased it in the cell lysates.

51 pattern of respective OH-metabolites in fly lysates.

52 g yeast, wheat germ, and rabbit reticulocyte lysates.

53 eracted with the P. falciparum-infected cell lysates.

54 coverage when applied to S. pombe whole cell lysates.

55 on of NTH1 activity in vitro and in cellular lysates.

56 ',4,6'-trichlorobiphenyl (3'-OHCB 28) in fly lysates.

57 cted immunoreactive IL-27 (953 +/- 504 pg/mg lysate), a mediator not previously associated with human

58 injected systemically, coupled with necrotic lysates, a higher number of large lesions was detected i

59 n the exosomal fraction from neuronal tissue lysates after spinal cord crush injury of mice.

60 tumor growth relative to simple mixtures of lysate and CpG-1826 (Lys-Mix) in both Py230 and Py8119 o

61 cantly, and simultaneously upregulated whole lysate and membrane portion NKCC1 protein expression.

62 g of alpha-mannosidases from both human cell lysate and mouse tissue extracts.

63 ion of proteins from minimal amounts of cell lysate and opens more opportunities for the isolation of

64 itro translation assay containing human cell lysate and purified target mRNA fused to a reporter was

65 ning a ribosome-depleted rabbit reticulocyte lysate and ribosomes prepared from HeLa or Huh-7.5 cells

66 oncentration was measured for mammalian cell lysate and serum, which led to estimates of low-mM ribos

67 trazole probe was also assessed in HeLa cell lysate and showed robust labeling only upon photoactivat

68 his iBody for the isolation of FAP from cell lysates and blood serum as well as for its detection by

69 as also measured by ELISA in bronchial/nasal lysates and by immunohistochemistry in bronchial tissue

70 and associated caspases in transgenic brain lysates and cells.

71 c comparison between metaphase-arrested cell lysates and chromosome-sorted samples reveals a cohort o

72 e mouse Htt transcripts directly from tissue lysates and demonstrate that this can replace the more w

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

74 e P300/CBP-associated factor (PCAF) in liver lysates and inhibited its activity in vitro This study t

75 by SuTEx fragments with site specificity in lysates and live cells to disrupt protein function.

76 V system, we purified AAVs from HEK293T cell lysates and medium by polyethylene glycol precipitation

77 also increased phospho-VEGFR2 in whole cell lysates and membrane fractions compared with control siR

78 ve assessment of all Htt transcripts in cell lysates and mouse tissues without the need to first extr

79 sed equivalent amounts of HgbA in whole-cell lysates and outer membranes.

80 In support of M2 polarization, PRF lysates and PRF conditioned medium enhanced the expressi

81 We report here that PRF lysates and PRF conditioned medium, the latter containin

82 aneous detection of two miRNAs in crude cell lysates and proved that the method was robust when used

83 agged cardiac myocyte ribosomes from cardiac lysates and subjecting the ribosome-protected mRNA fragm

84 Gag peptides were detectable in both cell lysates and supernatants in CD4+ T cells infected in vit

85 yn I serine 9, site 1, in the frontal cortex lysates and synaptosome preparations of male rhesus maca

86 uccessfully pull-down peptide-MHCs from cell lysates and the aAPCs generated using this technique wer

87 Pneumococcal lysates and the sputum fraction were separately evaluate

88 was verified with model samples of bacterial lysates and with four real-matrix samples of knee joint

89 in a crude cell lysate, RNA extract from the lysate, and a pure buffer.

90 idoyl fluoride electrophile, with human cell lysate, and the protein conjugates formed were identifie

91 sing co-IP using recombinant proteins, liver lysates, and mitochondria.

92 phosphopeptides in clinical specimens, cell lysates, and mouse liver tissue samples, demonstrating i

93 nd ELISA, we analyzed expression media, cell lysates, and purified proteins for FXII activation.

94 on of neutrophil elastase activity in tissue lysates, and we have applied it to demonstrate that this

95 ssolved organic carbon from Emiliana huxleyi lysates, and were conducted using surface-seawater colle

96 Previous investigations using Leishmania lysate antigen demonstrated that the immunoglobulin (Ig)

97 d immunosorbent assays (ELISAs) with rK39 or lysate antigens and novel IgG1 rK39 rapid diagnostic tes

98 e sought to evaluate the effect of bacterial lysate applied orally from the second until seventh mont

99 eds 10 pM while miRNA concentrations in cell lysates are below 1 pM.

100 Single-cell lysates are generated at defined time points and analyze

101 The lysates are identical to those used in Fig.

102 Together, these results show that the way lysates are processed and packaged has a profound impact

103 e assay-based kinome analysis (in which cell lysates are used to phosphorylate specific kinase substr

104 identifies native CAII in human kidney cell lysate as an AEBSA target.

105 g arachidonic acid as the substrate and worm lysate as source of enzyme(s).

106 against the gold standard Limulus Amoebocyte lysate assay in real bacteria culture containing natural

107 tally show that Ca2+ application to cellular lysates at physiological concentrations inhibits PP2C ac

108 -interactive proteins from the S. coelicolor lysate based on the tandem affinity purification (TAP).

109 Lysate-based cell-free systems have become a major platf

110 Levels of copper were measured in cell lysates, blood samples, liver homogenates, and subcellul

111 n HEK293T cells, we detected WT MESD in cell lysate but not in conditioned medium, whereas the conver

112 DH enzyme activity was detected in GV oocyte lysate, but CHDH became highly active during oocyte meio

113 o ability to suppress dicer activity in cell lysates, but higher expression of B2, following heat sho

114 o interrogate itaconate's reactivity in cell lysates, but methods for analyzing targets of itaconatio

115 on accurate miRNA quantitation in crude cell lysate by a CE-based hybridization assay termed direct q

116 ion of intracellular FA release through cell lysate calibration.

117 We also show that MDA-MB-231 cell lysates can "seed" aggregation of the central core domai

118 values for unpurified proteins in crude cell lysates can be obtained without prior knowledge of the c

119 emonstrated that human CBD and PSP tauopathy lysates (CBD-tau and PSP-tau) contain distinct tau strai

120 high quantity of mRNA from crude yeast cell lysate compared to a phenol/chloroform extraction method

121 oscopy and elemental Zn in bio-chelated cell lysate complex was confirmed by SEM and Energy Dispersiv

122 atly increased in Nf123aIN/23aIN mouse brain lysates, confirming that exon 23a inclusion inhibits Nf1

123 allergic parent received orally a bacterial lysate consisting of heat-killed Gram-negative Escherich

124 Addition of cell lysates containing baculovirus-expressed B2 to lysates f

125 We previously demonstrated that crude cell lysates could be used for some limited downstream DNA ap

126 dard data set and a public large-scale yeast lysate data set show that iTop-Q achieves highly accurat

127 mparison of adult bone marrow to fetal liver lysates demonstrated developmental silencing in IGF2BP1.

128 alyze the genome of SARS-CoV-2 in human cell lysate, demonstrating the capability and the utility of

129 al method for measuring enzyme activities in lysates derived from individual cells and will contribut

130 ides (CpG-1826) as adjuvants and encapsulate lysates derived from TNBC cell lines as antigens.

131 in-labeled viral dsRNA or poly(I.C) and cell lysate-derived or in vitro translated G3BP1 indicated th

132 of mdDiLeu-labeled Saccharomyces cerevisiae lysate digest on an Orbitrap Fusion Lumos mass spectrome

133 onectin by peritoneal cell-derived mast cell lysates diminished GBS adherence.

134 On-chip cell lysate electrical impedance spectroscopy has been utiliz

135 MDCK cells were inoculated with tissue lysates, enabling recovery of one IAV isolate confirmed

136 ines (MAV) prepared from S. pneumoniae TIGR4 lysates enriched for surface proteins by a chromatograph

137 In addition, our sensor could detect SP lysate even when dispersed in BSA or Escherichia coli ly

138 es of SGPs could be detected from total cell lysates, even at a signal-to-noise ratio of as low as 3:

139 CaMKII activity in hippocampal protein lysates exhibited a strain-dependence in Scn2a(Q54) mice

140 ein levels using 0.5 ug/sample total protein lysate extracted from 2 x 5 um FFPE slices absolutely an

141 with dried blood spot punches or fibroblast lysate followed by quantification of enzymatic products

142 r online detection of metabolites from tumor lysates following liquid chromatography (LC).

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

144 Following cell lysis and sampling crude cell lysate for analysis, the substrate and the product are s

145 -scale proteomics analysis of cell or tissue lysate for enhanced proteome coverage, particularly for

146 mensionality of datasets is shown using cell lysates for all possible combinations of up to 9 fingerp

147 f O-glycans from glycoproteins in whole cell lysates for mass spectrometric analysis.

148 mes and proteomes from detergent-free tissue lysates fractionated across a sucrose gradient.

149 It is based on cellular lysate fractionation by density gradient ultracentrifuga

150 Indeed, lysate from a zebrafish Staphylococcus isolate is suffic

151 ferently to syndecan-4 in the left ventricle lysate from aortic-banded heart failure (ABHF) rats comp

152 f both CXCR4 and CXCR7 compared with protein lysates from a nontumorigenic prostate epithelial cell l

153 The same lysates from a subset of matched samples were subjected

154 When scaffolds containing lysates from an insulin-producing beta-cell line were im

155 sates containing baculovirus-expressed B2 to lysates from dipteran (S2, Aag2) or lepidopteran (Sf9) c

156 in peripheral blood mononuclear cell (PBMC) lysates from individual donors.

157 ) using both recombinant enzymes and nuclear lysates from leukemia cells.

158 Size-exclusion chromatography of the lysates from mutant p53-containing breast cancer and ova

159 in receptors, a Clec2d reporter responded to lysates from necrotic cells.

160 e-affinity pulldown assays and proteomics of lysates from primary cortical neurons, we identified tha

161 ly, MLC2 phosphorylation was reduced in lung lysates from TIMAP-deficient mice and upon silencing of

162 ll types is challenging due to the fact that lysates from tissues always represent a mixture of cells

163 E. coli increased 5-oxoprolinase activity in lysates >/=1700-fold.

164 sis (HILIC-RPLC) of S. cerevisiae whole cell lysate has been used to acquire retention information fo

165 From whole tissues to single-cell lysate, heterogeneous immunoassays are widely utilized f

166 release of cytochrome c from mitochondria in lysates human embryonic kidney cells HEK293T.

167 d the presence of chlorotyrosine in the cell lysates, hypochlorous acid is hypothesized to be the che

168 Chemoproteomic analysis of cardiac lysates identified candidate ibrutinib targets, which we

169 detected in detergent-treated infected cell lysates.IMPORTANCE The entry of enveloped viruses is ach

170 roteoforms from 5 mug of intact E. coli cell lysate in 10 online-collected fractions.

171 exhibits good sensing performance toward SP lysate in a clinically relevant linear range from 5 to 1

172 Single-cell lysate in each microwell is "electrophoretically project

173 ng cation exchange-fractionated HEK293T cell lysate in XL-MS experiments using disuccinimidyl sulfoxi

174 eproducible near-complete digestion of cells lysates in 1-5 min.

175 compound 73 enriched NS4B protein from cell lysates in pull-down studies, and the findings together

176 tide-MHCs can directly be captured from cell lysates, including cancer cells using affinity beads, an

177 iple Dhb-modified proteins in mammalian cell lysates, including histone H3, a previously unknown targ

178 lli-Q(TM) water and the infiltration of cell lysate into the porous matrix was monitored by measuring

179 iently even after lysis of the cells, if the lysate is not protected from ambient light.

180 Less than 1 muL of cell lysate is required as starting material to solve the ato

181 ilitate priming anti- tumor T cells by tumor lysate-loaded DC vaccine.

182 toward the potential of oxidized tumor cell lysate-loaded SNAs as a potent class of immunotherapeuti

183 stant oligomers change in size over time and lysates made from de novo induced cultures are able to c

184 strated that, compared to standard bacterial lysates, MAV was enriched with Hsps and contained severa

185 tically significant cytochrome P450s in cell lysate, microsomes, and bacteria.

186 mple of bovine serum albumin (BSA) and yeast lysates mixed at different ratios.

187 Western blot analysis of total cell lysate obtained from normal human mammary epithelial (HM

188 popolysaccharides (LPS) with and without PRF lysates obtained by repeated freeze-thawing or the secre

189 ab27b protein levels were increased in brain lysates obtained from postmortem tissues of individuals

190 phA7 could be precipitated from the cellular lysate of BJAB cells using recombinant gH/gL, and knocko

191 of endogenous alpha-syn from red blood cells lysate of healthy controls and PD patients.

192 An oral bacterial lysate of heat-killed Gram-negative Escherichia coli and

193 Bruton's tyrosine kinase (BTK) in the blood lysate of monkeys after dosing with branebrutinib (BMS-9

194 mpanying HNSCC biomarkers from a single cell lysate of oral cancer cell cultures was demonstrated.

195 nents of PRC2, NuRD, and SIN3A from the cell lysate of the TNBC cell line SUM149.

196 abolome from the (12)C-/(13)C-dansyl labeled lysates of 100, 1000, and 10000 cells, respectively.

197 was then used to bind candidate ligands from lysates of activated monocytes and analyzed by mass spec

198 ining the inositol phosphate levels in brain lysates of animals previously treated with melatonin.

199 ever, many techniques analyze fixed cells or lysates of bulk populations, in which information about

200 Purified recombinant 3MST and lysates of COS cells expressing 3MST showed that Cys-SSH

201 Immunoprecipitation experiments with lysates of HSV-infected neurons showed that UL16 and thr

202 protein required further incubation with the lysates of human umbilical vein endothelial cells (HUVEC

203 Both whole cells and cell lysates of Oxf strains HC1 and OxWR were analyzed using

204 The immunomodulatory character of pancreatic lysates of patients with cancer differs from those with

205 oll-like receptor signaling were enriched in lysates of podocytes treated with the TrkC ligand neurot

206 P activity in both enzyme solutions and cell lysates of prostate cells.

207 se in CEST-MRI contrast was obtained in cell lysates of rdLRP transfected cells and in in vivo LRP ex

208 We show that lysates of RhCMV-infected cells contain an IgG-binding p

209 ody-based serotyping assay that uses culture lysates of Streptococcus pneumoniae This study describes

210 HIV trans-activation response element RNA in lysates of T cell lines or primary human CD4(+) T cells.

211 Cell lysates of the cyanobacterial mutants further functional

212 mining the numbers of CFU recovered from the lysates of the infected monolayers, by monitoring the le

213 tissue of patients with AF and from cardiac lysates of wild-type and Pln-knockout mice.

214 Addition of 2 mm ATP to the lysate or homogenate did not decrease the stability of t

215 n incubation with human lens-epithelial cell lysate or lens homogenate.

216 Cell lysate or mitochondria were isolated using standard tech

217 the form of a defined peptide antigen, cell lysates or antigens sourced from AML cells recruited in

218 d transformation results collected from cell lysates or fixed-cells conceal important dynamic informa

219 udy samples of limited lifetime such as cell lysates or whole cells.

220 ts as a biochemical precursor to NAD(+) Cell lysates possess an ATP-dependent kinase activity that ef

221 significantly increased cAMP levels in cell lysates prepared from inner medullary collecting duct (I

222 Measurements of enzyme activities in lysates prepared from transfected HEK293T cells expressi

223 ll types, nc886 bound to PKR in human T cell lysates, preventing PKR phosphorylation by polyinosinic:

224 MT 10-plex experiments with one microgram of lysate protein and 2000 sorted HeLa cells (roughly half

225 a linear range of 0.05-2.0 fmol/mug of total lysate protein and with coefficients of variation < 15%.

226 00 sorted HeLa cells (roughly half microgram lysate protein) in each channel, respectively.

227 ectrometric analysis indicated that 628 cell-lysate proteins enriched in 44 cellular component cluste

228 Cell-lysate proteins regulated by TGF-beta1 were characterise

229 nts with GBM undergoing treatment with tumor lysate-pulsed DC vaccination and PD-1 mAb blockade were

230 inimal experimental effort regardless of the lysate quality.

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

232 G and IgE antibody levels to whole bacterial lysate, recombinant P1 adhesin, and OVA.

233 f substance P, periostin, and red blood cell lysate (representing hemosiderin).

234 exes from as little as 4 micrograms of input lysate, representing a 50-100-fold downscaling compared

235 ucrose gradient fractionation of the nuclear lysate resolved several ribonucleoprotein (RNP) complexe

236 xcretion and respiration), viruses and viral lysate respectively.

237 rotein interactions in E. coli and HeLa cell lysates, respectively, identifying 1,158 and 3,301 uniqu

238 kinases and 15 lipid kinases from human cell lysates, respectively.

239 A-MB-231 xenografts were exposed to necrotic lysates, resulted in an increase in both proliferation a

240 determined for miRNA samples in a crude cell lysate, RNA extract from the lysate, and a pure buffer.

241 esolution reconstructions from a much cruder lysate sample.

242 which codes for the carbapenemase OXA-48, in lysate samples from Klebsiella pneumoniae.

243 LC/MS) quantifications of irinotecan in cell lysate samples were used to compare the results from Sin

244 d to detect pathogenic Leptospira whole cell lysates samples with the satisfactory results.

245 alization of BfrB-iron in P. aeruginosa cell lysates separated on native PAGE gels and stained for ir

246 Immunoprecipitation of ARC from mouse islet lysates showed ARC binds JNK, suggesting interaction bet

247 Western blot analysis of spleen lysates showed CD63 protein expression was reduced in a

248 Interestingly, ELISAs performed on BAL lysates showed protein levels may partly disagree with e

249 eover, the addition of purified RelE to cell lysates shows promise as a method for generating ribosom

250 rganic compounds and 0.2 mum filtered diatom lysate significantly enhanced the growth of this bacteri

251 mplexity were compared: (1) data from a cell lysate study performed in our lab, (2) data from an inte

252 ABPP on crude cell lysates suggested that general proteome thiol reactivity

253 d human patients compared with lymphoma cell lysates, suggesting a concentration of these factors ove

254 Moreover, PRF lysates suppressed the translocation of p65 from the cyt

255 ndent desuccinylation activity in crude cell lysate systems, as compared to the desuccinylation react

256 tion identified Hspb1 mRNA in wild-type lens lysate TDRD7-pulldowns, and single-molecule RNA imaging

257 tivities in dried blood spots and fibroblast lysates that allow newborn screening and diagnosis of al

258 ded cellular environment and eukaryotic cell lysates, that parameters optimized toward a pseudo first

259 protein could be obtained directly from cell lysates, thus leading to an improved method to recombina

260 for sensitive and selective analysis in cell lysates, tissues, and serums by mass spectrometry (MS).

261 We applied iTORC to a mouse hepatocyte lysate to identify known sulfenylated and disulfide-bond

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

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

264 an embryonic kidney cells and cardiac tissue lysates to enable the identification of 188 and 124 endo

265 RT-PCR of cell lysates transfected with rdLRP demonstrated a stable rep

266 egation of both model proteins and cytosolic lysates under standardized conditions.

267 ual SOS molecules are captured from raw cell lysate using Ras-functionalized supported membrane micro

268 n of inflammatory markers in the lung tissue lysates using reverse transcription quantitative polymer

269 man and mouse GBM extracellular nanovesicles lysates using the Ras-binding domain of Raf also copreci

270 lammatory cytokines were analyzed in corneal lysates using Western blot and Luminex assays.

271 lysis (SCX-RPLC) of S. cerevisiae whole cell lysate was used to generate a retention dataset of appro

272 The anti-inflammatory activity of PRF lysates was further confirmed by IL6 immunoassay.

273 o enrich members of the CDK family from cell lysates, was investigated.

274 labels for Rictor and mTOR in the whole cell lysate (WCL) blots were swapped in Fig.

275 In the analysis of MCF7 cell lysate, we show collision-induced dissociation (CID) and

276 te middle-range sized peptides from cellular lysates, we explored the use of the proteases Asp-N and

277 ced conversion assays with RML-infected cell lysates, we observed a strong signal over all six passag

278 .250 nM for drug-bound BTK (DB-BTK) in blood lysate were successfully achieved by using this IC-LC-MS

279 Whole cell protein lysates were collected and analysed using stabled isotop

280 increased levels of Cyc-D and p21 in spleen lysates were observed in animals administered control.

281 Further, Zn enriched cell lysates were prepared by Ultrasonication, as an organic

282 Bacterial lysates were probed by using Western blot analysis with

283 nd in complex environments of mammalian cell lysates, where relative amounts of free reactive oxygen

284 e spectral matches enriched from mouse brain lysates, which more than triples identifications from st

285 of BSH activity with purified protein, cell lysates, whole cells, and in human gut microbiome sample

286 ct derivatization of AP sites in the nuclear lysate with O-(pyridin-3-yl-methyl)hydroxylamine, yieldi

287 lon cancer cell lines and flash-frozen tumor lysates with a linear range of 0.05-2.0 fmol/mug of tota

288 using proteome-wide reactions of HT-29 cell lysates with a model probe of threonine beta-lactone.

289 The comparison of lysates with and without previous RNase treatment enable

290 ith Lys-SNAs and simple mixtures of oxidized lysates with CpG-1826.

291 IIA heavy chain coimmunoprecipitated from EC lysates with endogenous TIMAP, and endogenous MLC2 coloc

292 ne cells when compared to simple mixtures of lysates with linear oligonucleotides both in vitro and i

293 tion can be performed in blood serum or cell lysates with minimal interference from biomolecules.

294 tation of rat liver or transfected HeLa cell lysates with rOATP1A1 antibody specifically co-immunopre

295 simple implementation and rapid recovery of lysates without additional reagents.

296 concentrations in the culture media and cell lysates without changing the expression of 5-HT synthesi

297 European Commission) using raw mitochondrial lysates without DNA extraction or polymerase chain react

298 ates, and also allows the direct use of cell lysates without the need for DNA purification or nuclear

299 ies and identified 1861 proteoforms in yeast lysate, yielding an approximately 40% increase over the

300 ntibodies against LcrV, Y. pestis whole-cell lysate (YPL), and F1 antigen and more balanced IgG1:IgG2