ライフサイエンスコーパス: tryptic

1 Tryptic activity has been attributed to acidic Glu(226)

2 phate (NADPH), a polyene was detected in the tryptic acyl carrier protein (ACP).

3 lly demonstrate the lack of commutability of tryptic and cleavable SIL peptides as internal calibrato

4 Combined data from the tryptic and Glu-C endoproteinase digests of neuraminidas

5 The mixtures of ions generated by tryptic and peptic digestions of lysozyme and insulin, r

6 extraction of phosphopeptides from 40 muL of tryptic beta-casein digest using 70 mug of magnetic Ti-I

7 Unexpected tryptic cleavage has been characterized at modified K48

8 pectrometry because of the hydrophobicity of tryptic cleavage peptides on the one hand and the noncov

9 ease for rhEPO is compromised, as no natural tryptic cleavage site is located between the glycosylati

10 alkylation strategy to introduce artificial tryptic cleavage sites at Cys29 and Cys33 in rhEPO.

11 Hydrolysis rates at tryptic cleavage sites were also shown to be affected by

12 eptide products expected under commonly used tryptic conditions, we observe that peptides are formed

13 antimicrobial peptides with stability toward tryptic degradation.

14 a 1% false-discovery rate (FDR) from a yeast tryptic digest (95% confidence, p = 0.019).

15 rotein groups using only 100-1000 ng of HeLa tryptic digest (equivalent to ~500-5,000 cells).

16 ilico identify the peptides from the E. coli tryptic digest and show the increased confidence in pept

17 kephalin and angiotensin II, spiked in a BSA tryptic digest matrix at different concentrations.

18 ratio of IgG and bovine serum albumin (BSA) tryptic digest mixtures reached to 1:500.

19 Our method used a tryptic digest of 12 purified glycoproteins, glycopeptid

20 okinetic elution and sample stacking using a tryptic digest of 16 proteins to maximize peptide identi

21 ilar results were obtained when evaluating a tryptic digest of a cellular lysate, representing a more

22 strated by fractionating the separation of a tryptic digest of a known protein mixture onto the micro

23 electrospray interface for the analysis of a tryptic digest of a sample of intermediate protein compl

24 The intact and the tryptic digest of AuNCs@ew were characterized by mass sp

25 as performed in the presence of a background tryptic digest of bovine albumin.

26 Application of the method to a tryptic digest of bovine coagulation factor V resulted i

27 peptides from injection of only 1 pmol of a tryptic digest of bovine serum albumin using an eluent f

28 illary LC for the analysis of substance P, a tryptic digest of bovine serum albumin, and a phosphopep

29 LC-MS/MS analysis of a tryptic digest of BSA demonstrated that these cleavages

30 A Chromeo P503 labeled tryptic digest of BSA was used as a complex mixture to a

31 The approach is illustrated by examining a tryptic digest of cytochrome c and by identifying a pept

32 bilities of 2D FT-ICR MS are explored with a tryptic digest of cytochrome c with both ECD and IRMPD a

33 ber of peptides and proteins identified in a tryptic digest of E. coli cell lysate increased by 13% a

34 the enzyme transglutaminase 2) or the peptic-tryptic digest of gliadin (in native and deamidated form

35 selective enrichment of phosphopeptides from tryptic digest of standard protein (alpha-casein, beta-c

36 ll of reversed-phase C18 functionality) to a tryptic digest of whole Jurkat cell lysate to estimate t

37 muFFE analysis of a Chromeo P503-labeled BSA tryptic digest produced a 2D separation that made effect

38 anoLC-FAIMS-MS/MS of an unfractionated yeast tryptic digest using the modified FAIMS device identifie

39 xoid has been established by analysis of its tryptic digest using two-dimensional liquid chromatograp

40 eline resolved, and peptides from an albumin tryptic digest were much better resolved than with exist

41 t of casein phosphopeptides from a simulated tryptic digest with bovine serum albumin (BSA:casein, 10

42 ior to cleanup by immunoaffinity extraction, tryptic digest, and preconcentration by solid-phase extr

43 quantities (100 ng) of a Pyrococcus furiosus tryptic digest, but with mass-limited amounts (5 ng) CE

44 Employing a Saccharomyces cerevisiae tryptic digest, careful consideration of several perform

45 f small molecules and a bovine serum albumin tryptic digest, TASF improved the peak shape and resolut

46 tides as well as biological peptides bearing tryptic digest-like features and peptides with post-tran

47 with both peptide standards and a HeLa cell tryptic digest.

48 ted form, prepared in a bovine serum albumin tryptic digest.

49 tect sequences that are not accessible after tryptic digest.

50 mplarily shown for a pesticide mixture and a tryptic digest.

51 In the initial stage, markers from tryptic digested protein of chilled, boiled and autoclav

52 With only 100 mug of tryptic digested, nonstimulated HeLa protein and 45 h of

53 Tryptic-digested gelatins were measured using HPLC/MS an

54 tified and quantified the abundance of 1,056 tryptic-digested peptides, representing 163 proteins in

55 erwise, the reverse reaction occurred during tryptic digestion and analysis.

56 onto a polymer surface, followed by in situ tryptic digestion and comparative analysis using DESI-MS

57 on blocks lysine side chains, and subsequent tryptic digestion and N-terminal peptide derivatization

58 , ubiquitinated peptides were enriched after tryptic digestion by peptide immunoprecipitation using a

59 Global tryptic digestion followed by liquid chromatographic/mas

60 We performed GeLC-MS/MS (in-gel tryptic digestion followed by liquid chromatography-tand

61 nocysteine (U, SeCys), were identified after tryptic digestion followed by their separation.

62 Our results demonstrate that LFASP-based tryptic digestion is efficient, robust, reproducible, an

63 sity coating, while the SPME protocol on the tryptic digestion of a protein supported that enzymes we

64 In silico tryptic digestion of amaranth globulins was carried out

65 Tryptic digestion of differentially labeled carbonic anh

66 tion of mAbs with intact disulfide bonds and tryptic digestion of mAbs after reduction and alkylation

67 The workflow comprises a 2 h tryptic digestion of PAPs in suspension, an immunoaffini

68 nd sequencing of phosphopeptides obtained by tryptic digestion of protein extracts from HeLa cells.

69 to dissociate ADA-drug bindings, followed by tryptic digestion of protein pellets and subsequent LC-M

70 of small molecules and peptides obtained by tryptic digestion of proteins and entire proteins.

71 em can realize rapid, efficient and reusable tryptic digestion of proteins by taking advantage of its

72 technique for protein separation, and in-gel tryptic digestion of resolved protein bands has enhanced

73 This prediction was verified by tryptic digestion of SERT-expressing membranes: in the a

74 the determination of thiolic peptides after tryptic digestion of serum albumins from different speci

75 alyzing conserved peptides, derived from the tryptic digestion of the B subunits.

76 Tryptic digestion of the CYP3A4-[(3)H]ritonavir incubati

77 chromatography (IMAC), which was followed by tryptic digestion of the enriched sample and quantificat

78 Carbamylation of proteins followed by tryptic digestion produced peptides similar to those exp

79 ed by MALDI-TOF mass spectrometry, and their tryptic digestion products sequenced via Shotgun proteom

80 Tryptic digestion products were sampled, detected, and i

81 s were generated based on a previous limited tryptic digestion result and hydrogen-deuterium exchange

82 ication of 10 pg/mL, while introduction of a tryptic digestion step, followed by quantification of a

83 ids reformation of disulfide bonds to enable tryptic digestion without alkylation of cysteine residue

84 the performance of "bottom-up" (in-solution tryptic digestion), "top-down" (intact protein fragmenta

85 ltistep sample cleanup at the protein level, tryptic digestion, and isotope dilution mass spectrometr

86 atography of protein on cobalt-loaded beads, tryptic digestion, and MALDI MS analysis are performed i

87 Biomarker peptides were selected, after tryptic digestion, and quantified by multitarget nanoHPL

88 al approach via immunoaffinity purification, tryptic digestion, and subsequent detection by HPLC-HRMS

89 only used in protein solubilization prior to tryptic digestion, but the presence of the DS(-) hampers

90 This method involves optimization of in situ tryptic digestion, followed by reproducible and uniform

91 radigm of chemical cross-linking followed by tryptic digestion, mass spectrometry, and database searc

92 h an orthogonal traceable method using total tryptic digestion, peptide separation, and isotope dilut

93 mization of the conditions of extraction and tryptic digestion, restructured meat and blank values (t

94 otocol, which includes cell lysis, overnight tryptic digestion, sample analysis and database searchin

95 by the Fe3O4@Al2O3 MNPs followed by on-plate tryptic digestion, selective enrichment, and MALDI-MS an

96 lly toxic epitopes released after peptic and tryptic digestion, showing inefficiency as a treatment t

97 Selective elution of captured protein, tryptic digestion, tandem mass spectrometry analysis, an

98 re used to show that after glycinylation and tryptic digestion, the mass spectrometric response from

99 After protein extraction and tryptic digestion, three to four selected marker peptide

100 sis of a LLDGSSTEIR glycopeptide released by tryptic digestion, which carried two variant structures,

101 BSA peptides were generated by tryptic digestion.

102 njunction with endoglycosidase treatment and tryptic digestion.

103 in comparison to the commonly used one-step tryptic digestion.

104 hat can be robustly detected following rapid tryptic digestion.

105 uction products, which were stable following tryptic digestion.

106 turn structure and the stereoselectivity of tryptic digestion.

107 cular species derived from trastuzumab after tryptic digestion: a stable signature peptide (FTISADTSK

108 ences in relative peptide concentrations for tryptic digestions ranging from 15 min to 48 h.

109 mics experiments rely on prefractionation of tryptic digests before online liquid chromatography-mass

110 ntiated from nonmodified peptides in complex tryptic digests created upon proteolysis of proteins aft

111 online LC-MS analysis of hemoglobin and its tryptic digests directly from microliters of blood, achi

112 produce missed cleavage peptides in protein tryptic digests even at prolonged digestion times.

113 s pump to perform nanoflow HPLC separations; tryptic digests of bovine serum albumin (BSA), transferr

114 In-solution tryptic digests of cooked meats were deposited onto a po

115 Tryptic digests of fibrin that underwent differential cr

116 sites are enriched by the modified tips from tryptic digests of horse radish peroxidase, chicken avid

117 uantitating, and annotating Cys34 adducts in tryptic digests of human serum/plasma.

118 n sites after ablation of CypD, we subjected tryptic digests of isolated cardiac mitochondria from wi

119 The yielded tryptic digests of proteins were analysed by CZE in four

120 Therefore, tryptic digests of regular and hay milk were analyzed by

121 The standard peptide mixtures and tryptic digests of samples of different origins were sep

122 Peptide mapping of tryptic digests of the inactivated CYP2B6 using electros

123 S) cross-linked precursors, derived from the tryptic digests of three model proteins (Human Serum Alb

124 k areas of the two transition fragments from tryptic digests of whey proteins in stored milk protein

125 furosine results indicated that MRM based on tryptic digests of whole products was a feasible method

126 ides from human serum immunoglobulin G (IgG) tryptic digests were obviously observed with greatly imp

127 Tryptic digests were prepared in 50 mM formic acid and l

128 Meat tryptic digests were subjected to peptidomics analysis b

129 m fetuin, glycophorin A, ovalbumin and gp120 tryptic digests were used to build a spectral database o

130 The strategy includes periodate oxidation of tryptic digests, solid-phase enrichment of glycopeptides

131 Dissociation (HCD) spectra or spectra of non-tryptic digests.

132 s conducted with peptide solutions mimicking tryptic digests.

133 verified using standard peptides and protein tryptic digests.

134 romatography/tandem mass spectrometry of NFT tryptic digests.

135 Tryptic footprinting suggested that S-hexadecyl-CoA indu

136 n of the epitope, we isolated immunoreactive tryptic fragments by Western blotting and analyzed them

137 this reagent are easily separated from other tryptic fragments using strong cation exchange chromatog

138 synthetic peptides with the sequence of the tryptic fragments.

139 In the second step, tryptic gelatin peptides were separated and analyzed wit

140 hieved, which led to the identification of 7 tryptic glycopeptides from HRP and 16 glycopeptides from

141 IgG tryptic glycopeptides were analyzed by liquid chromatogr

142 lumn for the proteomics analysis of 10 ng of tryptic HeLa cell digest.

143 of potential anti-inflammatory activities in tryptic hydrolysates of bovine beta-casein.

144 eparation and characterisation of enzymatic (tryptic) hydrolysates of water-soluble proteins from Bac

145 and beta-CN 30-50 showed resistance to both tryptic hydrolysis and simulated digestion.

146 homology in the phosphopeptides released by tryptic hydrolysis and simulated gastrointestinal digest

147 enatured proteins were used as substrate for tryptic hydrolysis and the hydrolysis progress was chara

148 The casein by-product was submitted to tryptic hydrolysis for 30, 60 and 120min and further pre

149 The tryptic-hydrolyzed peptides were quantified using LC-MS/

150 w subclass-specific MALDI-TOF-MS analysis of tryptic IgG glycopeptides.

151 d that doxycycline can inhibit activation of tryptic KLKs through an indirect mechanism by inhibition

152 live keratinocytes during the production of tryptic KLKs, this treatment indirectly resulted in decr

153 the Orbitrap while simultaneously analyzing tryptic-like peptides using the ion trap.

154 chicken, and turkey) was developed using six tryptic marker peptides (8-11 amino acids).

155 bin in restructured meat was developed using tryptic marker peptides of TG (five markers), and bovine

156 e through identification of peptides without tryptic miscleavages or posttranslational modifications,

157 It also differs from human in resisting tryptic peptidase inhibitors (e.g., aprotinin), while fa

158 arapsins are conserved, inhibitor-resistant, tryptic peptidases.

159 Levels of the tryptic peptide ALFDFLK, found in the schizophrenia risk

160 nal activation of modified lysine-terminated tryptic peptide anions is consistent with a covalent mod

161 ed multiple reaction monitoring quantitative tryptic peptide assays were developed for each phosphory

162 ein concentration was shown to be unequal to tryptic peptide concentrations for most peptides, includ

163 ometry (LC-MS) with tandem MS (MS/MS) of the tryptic peptide containing the intramolecular disulfide

164 pproach simplified the detection of glycated tryptic peptide elution in the LC/MS analysis by giving

165 ine resolve four distinct sets of Abeta17-28 tryptic peptide epimers on a rapid (~1 s) time scale.

166 to analysis by MALDI-TOF mass spectrometry, tryptic peptide fingerprinting, molecular characterizati

167 ne strong cation exchange chromatography for tryptic peptide fractionation and combining it with the

168 ectrometry/mass spectrometry analysis on the tryptic peptide fragments indicates that the 3-fluorosia

169 E to the mobile phase of nLC/MS experiments, tryptic peptide identifications increased from 93 to 111

170 ble-isotope-labeled standard for every ricin tryptic peptide in the sample.

171 ss spectrometry (IMS-MS) study revealed that tryptic peptide ions containing a proline residue at the

172 ser desorption/ionization (AP-MALDI)-derived tryptic peptide ions have been subjected to ion/ion reac

173 study the peptide QPSSSR, a very hydrophilic tryptic peptide located on the C-terminus of the G prote

174 A tryptic peptide map identified two isoAsp-containing pep

175 Tryptic peptide mapping and tandem mass sequencing were

176 The most robust tryptic peptide marker in the validation was LTLGSALAAPQ

177 LC-MS/MS pipeline to identify taxon-specific tryptic peptide markers for the identification of Salmon

178 roscopy, separated protein fluorescence, and tryptic peptide modification in liquid chromatography-ta

179 In PAL experiments with SIRT2, a tryptic peptide originating from the covalent attachment

180 raction and purification were tested and the tryptic peptide pools were analysed by untargeted high r

181 single artificial protein to create internal tryptic peptide standards for MS as well as an intact pr

182 digestion and quantitation of a NGF-derived tryptic peptide via high-flow peptide immunoaffinity enr

183 s in the mass spectra of this doubly charged tryptic peptide, based solely on its amino acid sequence

184 nd MeArg were not found together on the same tryptic peptide, suggesting reciprocal regulation of the

185 +0) to six amino acid residues (+6) for each tryptic peptide.

186 oaches using selected reaction monitoring of tryptic peptides (also known as bottom up) have become c

187 d substrate ssDNA bind to the same three A3G tryptic peptides (amino acids 181-194, 314-320, and 345-

188 onditions and analyzing the MS/MS spectra of tryptic peptides allow an easy and high-throughput asses

189 meTools synthetic peptide library to 550,000 tryptic peptides and 21 million high-quality tandem mass

190 hout enrichment of glycopeptides from global tryptic peptides and at a false discovery rate of 1%, 10

191 as obtained using PACE-MSI for both digested tryptic peptides and endogenous neuropeptides from compl

192 sylation sites were separated from all other tryptic peptides and identified using MS data.

193 By isolating the tryptic peptides and subjecting them to Edman sequence a

194 Tryptic peptides are generated from tissue foci by apply

195 teins and direct detection of lipid-modified tryptic peptides by mass spectrometry.

196 n this study, we optimized a method to image tryptic peptides by matrix-assisted laser desorption ion

197 sp. NRC-1 and identified the sequence of 23 tryptic peptides by nano-liquid chromatography electrosp

198 ed the mass distributions of all theoretical tryptic peptides composed of 20 natural amino acids and

199 tial analysis of 20 samples containing 10 ng tryptic peptides demonstrated high reproducibility with

200 the analysis of coeluting model peptides and tryptic peptides derived from human plasma proteins, all

201 no acid pools in barley leaves and then into tryptic peptides derived from newly synthesized proteins

202 CID as the unmodified cations for the small tryptic peptides examined here and more sequence informa

203 artificial proteins that are concatamers of tryptic peptides for several proteins.

204 Through a PACE separation, 46 tryptic peptides from bovine serum albumin and 150 putat

205 esulting peptide anions, as demonstrated for tryptic peptides from bovine serum albumin and Halobacte

206 y, was evaluated using a mixture composed of tryptic peptides from caseins, bovine serum albumin, and

207 ed deamidation half-life for three different tryptic peptides from collagen (I) ranged from 2000 to 6

208 even (15)N-labeled QconCATs that cover seven tryptic peptides from human clusterin with a length of n

209 samples containing approximately 100 mug of tryptic peptides from mouse cerebrocortical brain tissue

210 five pH bumps were applied to elute E. coli tryptic peptides from the monolith, followed by analysis

211 derivatives and the production of different tryptic peptides from the unmodified and modified versio

212 Analysis of tryptic peptides from various fractions further confirme

213 For this purpose, tryptic peptides from whole cell lysates were analyzed b

214 C) was demonstrated from as little as 25 mug tryptic peptides from whole cell lysates.

215 Modified arginine-terminated tryptic peptides have shown evidence of a covalent modif

216 eries of epitope sequences concatenated with tryptic peptides in a single artificial protein to creat

217 LC-MS analysis of nonreduced tryptic peptides indicated trisulfide bonds are associat

218 of the serum protein and indirectly with the tryptic peptides measured by MS.

219 LC-MS/MS analysis of the tryptic peptides obtained from the in vitro ubiquitinate

220 ometer and applied for the separation of the tryptic peptides of a six-protein mixture and for the pr

221 Selected tryptic peptides of beta-Lg (ALPMHIR, LIVTQTMK and VLVLD

222 the tested BGEs, the best resolution of the tryptic peptides of extracted proteins of the above thre

223 HPLC analysis of tryptic peptides of FSBA-modified enzyme revealed the pr

224 untargeted "adductomics" method detected 50 tryptic peptides of HSA, containing Cys34 and prominent

225 Selected resolved tryptic peptides of proteins were characterised by effec

226 MS method for the direct detection of unique tryptic peptides of the KPC protein in clinical bacteria

227 ion concatamer (QconCAT) carrying prototypic tryptic peptides of UCH-L1 was used as an internal stand

228 lyze an interference model system comprising tryptic peptides of yeast that we contaminated with huma

229 digestion with trypsin, and stabilization of tryptic peptides on solid-phase extraction sorbent.

230 times the peptides were observed relative to tryptic peptides or those guanidinated with the conventi

231 Application of this method to tryptic peptides originating from O-GlcNAcylated protein

232 oteome level by examining the quality of the tryptic peptides prepared by on-surface nanodiamond dige

233 he LC/MS/MS analysis of the affinity-labeled tryptic peptides purified from HPLC, identified two majo

234 spectrometry analysis of >330,000 synthetic tryptic peptides representing essentially all canonical

235 mass spectrometry for the direct measure of tryptic peptides representing the amounts of specific pr

236 APP-QconCAT includes tryptic peptides that are common for all isoforms of APP

237 all isoforms of APP concatenated with those tryptic peptides that are unique for specific APP isofor

238 es were driven by the spatial orientation of tryptic peptides upon interaction with the negatively ch

239 igestion, online enrichment of IL-21 derived tryptic peptides using antipeptide antibodies, and quant

240 eptides in addition to a complex mixtures of tryptic peptides using LC-MS/MS, showing not only that A

241 arge proteomic retention data set of ~30 000 tryptic peptides was collected for each 2D pairing.

242 Separation of tryptic peptides was realized using a MicroHPLC interfac

243 motifs in interacting proteins, their unique tryptic peptides were analyzed by the motif scan softwar

244 The tryptic peptides were chromatographically separated with

245 by one-dimensional gel electrophoresis, and tryptic peptides were extracted from gel slices and anal

246 ristics of these standards and collection of tryptic peptides were mapped into hydrophobicity index (

247 were digested, and evolutionarily conserved tryptic peptides were quantified using isotope-dilution

248 ction; (iii) enrichment of the biotin-tagged tryptic peptides with streptavidin; (iv) liquid chromato

249 cal lengths (e.g. shorter/longer than common tryptic peptides) and lack of tryptic residues to facili

250 tein sequence up to 28 residues, overlapping tryptic peptides, and cyanogen bromide (CNBr) peptides.

251 sotopic tags to both the N- and C-termini of tryptic peptides, and second, a search engine (based on

252 Stable isotopically labeled (SIL) tryptic peptides, cleavable SIL peptides, and a full-len

253 ography tandem mass spectrometry analysis of tryptic peptides, followed by searching an appropriate s

254 For freebase guanidinated BSA tryptic peptides, more than 6-times the peptides were ob

255 ~1000 proteins reliably using only 75 pg of tryptic peptides, representing a 10-100-fold sensitivity

256 nown histone H3/H4 acetylated and methylated tryptic peptides, we identified novel H3 K18 methylation

257 ntified in acidic fractions from analysis of tryptic peptides.

258 bearing characteristics very different from tryptic peptides.

259 s to compare yields of numerous varieties of tryptic peptides.

260 tation and by mass spectroscopic analysis of tryptic peptides.

261 block both N-termini and lysine residues of tryptic peptides.

262 and more sequence information for the large tryptic peptides.

263 to enhance MALDI tandem mass spectrometry of tryptic peptides.

264 es of elastase to specifically target larger tryptic peptides.

265 ication of isoforms of threonine residues in tryptic peptides.

266 nalysis of typically much smaller unmodified tryptic peptides.

267 LIC models developed for complex mixtures of tryptic peptides.

268 ibed for a collection of approximately 40000 tryptic peptides.

269 lision Induced Dissociation (CID) spectra of tryptic peptides], their performance often deteriorates

270 by two-dimensional thin layer chromatography tryptic phosphopeptide profiles suggested that Ser-395 w

271 ied the ratio of (18)O- versus (16)O-labeled tryptic phosphopeptide using high mass accuracy mass spe

272 by reversed phase HPLC mass spectrometry in tryptic plasma digests.

273 In particular, the tryptic products of all seven of the lysine-linked dimer

274 gineer the sequence of EsxA to add desirable tryptic properties aimed at improving complex MS analysi

275 ntitative differences in CZE-UV profiling of tryptic protein digests were found, which can be potenti

276 y-mass spectrometry (IMS-IMS-MS) analyses of tryptic protein digests.

277 evidence of T cell activation by peptic and tryptic (PT) digests of gliadins from 2 monococcum lines

278 er than common tryptic peptides) and lack of tryptic residues to facilitate peptide ionization/fragme

279 at the cleavage site, in agreement with the tryptic serine protease activity of FVIIa.

280 n kallikrein-related peptidase 2 (KLK2) is a tryptic serine protease predominantly expressed in prost

281 important means of evolving new functions of tryptic serine proteases from transmembrane ancestors.

282 t, because citrullination eliminates arginyl tryptic sites.

283 c expression of mutant SUMOs with introduced tryptic sites.

284 were dissected, homogenized, and cultured in tryptic soy agar medium.

285 Colonies from tryptic soy agar with 5% sheep blood (blood agar) and Ma

286 . Pharmacopeia (USP) chapter <797> calls for tryptic soy agar with polysorbate and lecithin (TSApl) f

287 inhibited 82.8% of C. perfringens growth in Tryptic Soy Broth (P < 0.05).

288 sms in double-distilled water (ddH2O) versus tryptic soy broth (TSB) to incubate disks, and incubatio

289 n several formulations of 4 different media (tryptic soy broth (TSB), brain-heart infusion (BHI), Lur

290 in two growth media, lysogeny broth (LB) and tryptic soy broth (TSB).

291 s and Escherichia coli O157:H7 cultivated in tryptic soy broth at 4, 22, and 35 degrees C for up to 7

292 to current for 24 hours in 1/10(th) strength tryptic soy broth containing 9 g/L total NaCl.

293 g of two 45-min exposures per 24-h period in tryptic soy broth followed by immersion in a remineraliz

294 To detect the VRE subpopulation, tryptic soy broth was inoculated from positive blood cul

295 bapenem inactivation method (mCIM), in which tryptic soy broth was substituted for water during the i

296 ease in biofilm density in cells cultured in tryptic soy broth with 1% glucose (TSBG) when selenite w

297 obial activities of nanoemulsions and LAE in tryptic soy broth.

298 Furthermore, the tryptic stability of the IDR-1018 derivatives was assess

299 ies against bacterial superbugs, display low tryptic stability.

300 Soluble mouse and human marapsins are tryptic with subsite preferences distinct from those of