ライフサイエンスコーパス: tryptic

1 non-tryptic (AAHAL, AHAAL, AHADL, AHDAL) and tryptic (AAAHK, AAHAK, AHAAK, HAAAK, AAAHR, AAHAR, AHAAR

2 stidine-containing pentapeptides of both non-tryptic (AAHAL, AHAAL, AHADL, AHDAL) and tryptic (AAAHK,

3 226)Glu mutants of mouse cathepsin G acquire tryptic activity and human ability to activate prourokin

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

5 ed an apparently unprecedented way to create tryptic activity in a serine peptidase.

6 We propose that tryptic activity is not an attribute of ancestral mammal

7 Ala(226) for Glu(226), suggesting that human tryptic activity may be anomalous.

8 activity and selectivity and near absence of tryptic activity.

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

10 lowly digested at 1 to 2 out of 14 potential tryptic and chymotryptic cleavage sites under duodenal c

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

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

13 , accounting for the specific orientation of tryptic and Lys-C peptides.

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

15 -faced" ability to cleave peptides at basic (tryptic) as well as aromatic (chymotryptic) sites.

16 Unexpected tryptic cleavage has been characterized at modified K48

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

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

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

20 antimicrobial peptides with stability toward tryptic degradation.

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

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

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

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

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

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

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

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

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

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

31 yses of complex biological samples such as a tryptic digest of bovine serum albumin and a carnitine s

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

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

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

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

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

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

38 ion trap mass spectrometry and compared to a tryptic digest of Deinococcus radiodurans.

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

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

41 The approach was tested on tryptic digest of Saccharomyces cerevisiae histones.

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

43 D LC-MS/MS) approach was used to analyze the tryptic digest of toxoid as a whole.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

63 Global tryptic digestion followed by liquid chromatographic/mas

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

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

66 In silico tryptic digestion of amaranth globulins was carried out

67 Tryptic digestion of differentially labeled carbonic anh

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

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

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

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

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

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

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

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

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

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

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

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

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 The tryptic digestion was physiologically significant, corre

84 olyzing succinimide in H(2)(18)O followed by tryptic digestion were used to label and identify the si

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

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

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

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

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

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

98 BSA peptides were generated by tryptic digestion.

99 hat can be robustly detected following rapid tryptic digestion.

100 njunction with endoglycosidase treatment and tryptic digestion.

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

102 uction products, which were stable following tryptic digestion.

103 turn structure and the stereoselectivity of tryptic digestion.

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

105 n in a high boiling point solvent, and (iii) tryptic digestions of cytochrome c at 22 and 40 degrees

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

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

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

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

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

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

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

113 Tryptic digests of fibrin that underwent differential cr

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

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

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

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

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

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

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

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

122 The method was evaluated using tryptic digests of yeast enolase and alcohol dehydrogena

123 l 60 F(254S) plate and peptides from protein tryptic digests separated on a ProteoChrom HPTLC Silica

124 9 and 12 amino acids that represent typical tryptic digests were designed, synthesized, and analyzed

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

126 Meat tryptic digests were subjected to peptidomics analysis b

127 with trypsin in protonated solution, and the tryptic digests were then analyzed via liquid chromatogr

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

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

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

131 s conducted with peptide solutions mimicking tryptic digests.

132 verified using standard peptides and protein tryptic digests.

133 romatography/tandem mass spectrometry of NFT tryptic digests.

134 Tryptic footprinting suggested that S-hexadecyl-CoA indu

135 eased the formation of the 95-kDa C-terminal tryptic fragment when detected by an Ab directed at a C-

136 The protein tryptic fragments and their modification products were a

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

138 toxin's natural RNA target, and analysis of tryptic fragments of the toxin itself.

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

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

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

142 IgG tryptic glycopeptides were analyzed by liquid chromatogr

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

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

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

152 ving as orientation probes, indicate that in tryptic/Lys-C peptides the C-terminal carboxyl group app

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

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

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

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

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

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

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

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

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

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

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

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

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

166 intact proteins and/or an LC-MS analysis of tryptic peptide fragments generated after the oxidation

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

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

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

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

171 viously been shown that photodissociation of tryptic peptide ions with 157 nm light in a matrix-assis

172 A tryptic peptide map identified two isoAsp-containing pep

173 Tryptic peptide mapping and tandem mass sequencing were

174 rom cation-exchange chromatography (CEX) and tryptic peptide maps generated with the new digestion me

175 of the extracted ion chromatograms from the tryptic peptide maps.

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

177 eptide analytes from both simple and complex tryptic peptide matrices using selected reaction monitor

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

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

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

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

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

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

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

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

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

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

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

191 sing mass spectra of the cysteine-containing tryptic peptides and used to follow the unfolding of eac

192 g synthetic heavy isotope-labeled C-terminal tryptic peptides as spiked standards with a triple quadr

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

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

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

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

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

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

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

200 ent sequencing approach, a collection of 266 tryptic peptides from 23 model proteins were analyzed an

201 In the analysis of 31 tryptic peptides from 4 model proteins, the algorithm id

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

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

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

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

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

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

208 gradation and mass spectrometric analyses of tryptic peptides from rat DSP-PG, along with substitutio

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

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

211 Analysis of tryptic peptides from various fractions further confirme

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

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

214 Differential dimethyl labeling of tryptic peptides generated from the purified therapeutic

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 sured both the quantity and kinetics of SP-B tryptic peptides in tracheal aspirate samples of symptom

218 All tryptic peptides including N-terminal, C-terminal, and m

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

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

221 substance P peptide, as well as a mixture of tryptic peptides obtained by enzymatic digestion of cyto

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

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

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

225 An analysis of the tryptic peptides of cytochrome c formed by both ESI and

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

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

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

229 Selected resolved tryptic peptides of proteins were characterised by effec

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

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

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

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

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

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

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

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

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

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

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

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

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 excised, and Ala-/Gly-rich, allele-specific tryptic peptides were identified by liquid chromatograph

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

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

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

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

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

256 age intensities of spiked synthetic catalase tryptic peptides, which we used as an internal standard,

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

258 tation and by mass spectroscopic analysis of tryptic peptides.

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

260 LIC models developed for complex mixtures of tryptic peptides.

261 and more sequence information for the large tryptic peptides.

262 to enhance MALDI tandem mass spectrometry of tryptic peptides.

263 -activated dissociation (CAD) spectra of the tryptic peptides.

264 observed for arginine- and lysine-terminated tryptic peptides.

265 ibed for a collection of approximately 40000 tryptic peptides.

266 ntified in acidic fractions from analysis of tryptic peptides.

267 bearing characteristics very different from tryptic peptides.

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

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

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

271 Tryptic phosphopeptides (immobilized metal affinity chro

272 The sizes of the tryptic phosphopeptides derived from Nup62 were compatib

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

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

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

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

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

278 sed to filter for phosphorylated peptides in tryptic protein digests.

279 The role of tryptic proteolysis in bottom-up shotgun proteomics and

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

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

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

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

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

285 c expression of mutant SUMOs with introduced tryptic sites.

286 t, because citrullination eliminates arginyl tryptic sites.

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

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

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

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

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

292 ns by 2 methods: (i) inoculation of swabs in tryptic soy broth containing 2 microg/ml imipenem follow

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

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

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

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

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

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

299 ies against bacterial superbugs, display low tryptic stability.

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