ライフサイエンスコーパス: agar

1 pplemented with 0.01% (w/v) cholesterol (LBC agar).

2 richment followed by plating to Baird-Parker agar.

3 form xenografts in mice and colonies in soft agar.

4 an overgrowth phenotype, and growth in soft agar.

5 es than they did on sheep blood or chocolate agar.

6 n IRS1 activity for colony formation in soft agar.

7 mple directly plated for growth on chocolate agar.

8 erial colonies (Escherichia coli) growing on agar.

9 sisting of pH-buffered deoxygenated sulfidic agar.

10 he filter membrane was plated onto selective agar.

11 tic colonies appearing the next day on blood agar.

12 s escape flares from mixed inocula seeded on agar.

13 nhances the ability to form colonies in soft agar.

14 d to a reduction of colony formation in soft agar.

15 to xylose lysine desoxycholate and MacConkey agar.

16 ic activity in the DeltavfrB mutant on blood agar.

17 ansplanted mice formed colonies in semisolid agar.

18 ter surfaces and medium solidified with 1.5% agar.

19 solubilizing the cholesterol micelles in LBC agar.

20 oma proliferation in both monolayer and soft agar.

21 h subculture on Mycoplasma-specific Hayflick agar.

22 s colony-forming units (cfus) when plated on agar.

23 um-stimulated epithelial cell growth in soft agar.

24 pontaneous mutants able to move through soft agar.

25 H9 broth and 7H10 agar or 7H9 broth and 7H11 agar.

26 rook 7H11 and Burkholderia cepacia selective agars.

27 and Eggerthella lenta (broth, 1 to 4 mug/ml; agar, 1 to 8 mug/ml) were approved by the Clinical and L

28 30 degrees C, 64.7%; P = 0.005), and in BHI agar (63.0%; P = 0.001).

29 le esculin azide agar with vancomycin (BEAV) agar (84.8%) for detecting vancomycin-resistant enteroco

30 were able to detect 25 fmol of Rhodamine in agar ablation experiments.

31 The effects of agar, alginate, lecithin and glycerol on the rheological

32 tb fail to resume replication when plated on agar, although their viability is demonstrable by other

33 d for bedaquiline MICs determined using 7H10 agar and 7H11 agar but not for bedaquiline MICs determin

34 This study also showed that agar and alginate in addition to potato puree could be v

35 and inoculated on MacConkey agar, Chocolate agar and Blood agar culture Medias.

36 nd displayed increased clonogenicity in soft agar and broad drug-resistance in vitro and in vivo.

37 , Italy) software to analyze VRE chromogenic agar and compared the results to technologist plate read

38 rculosis in sputum, in comparison with solid agar and liquid culture.

39 We studied P. aeruginosa isolates grown in agar and mucus gels containing sputum from patients with

40 rs, but developed into colonospheres in soft agar and nodules/tumors in nude mice.

41 monolayers as well as colonospheres in soft agar and nodules/tumors in nude mice.

42 ted CTSD induction, inhibited growth in soft agar and partially restored tamoxifen sensitivity of res

43 itative analysis of hemolysis on sheep blood agar and quantitative measurement of cytolysis of human

44 ls contained HPV-16, formed colonies in soft agar and rapidly produced tumors in immunodeficient mice

45 f yeast colonies for various combinations of agar and sugar concentrations.

46 hat cause the worm's body to settle into the agar and the resulting dynamics of groove formation.

47 for serial sputum colony counting (SSCC) on agar and time-to positivity (TTP) measurement in mycobac

48 ity of tumorigenic rat cells to grow in soft agar and to form tumors.

49 cycline on blood-supplemented Mueller-Hinton agar and to the inhibitory effects of metronidazole at 1

50 TGM2 suppressed colony formation in soft agar and tumor formation in a xenograft mouse model.

51 teristics and inhibited their growth in soft agar and tumor growth in vivo.

52 t formed significantly more colonies in soft agar and were significantly more invasive when grown in

53 rent volumes of urine onto 7 combinations of agars and environments.

54 al culture techniques (aerobic and anaerobic agars and thioglycolate broth) compared to inoculation i

55 ration, anchorage-independent growth in soft agar, and enhanced metastatic potential.

56 rmined by plating homogenates onto MacConkey agar, and immunofluorescence microscopy performed using

57 creased anchorage-independent growth in soft agar, and increased migration.

58 ion, enhanced tumor colony formation in soft agar, and increased xenograft tumor growth in nude mice.

59 l proliferation and colony formation in soft agar, and induces apoptosis in cancer cells.

60 liferation, reduced colony formation in soft agar, and induction of apoptosis.

61 in culture, reduced colony formation in soft agar, and inhibited invasion of melanoma cells.

62 ted using a "naked" PAO chip placed on solid agar, and later in a chip encased in a specially designe

63 cquired anchorage-independent growth in soft agar, and led to enlarged, disorganized, three-dimension

64 including conventional culture, chromogenic agar, and polymerase chain reaction.

65 eeded for formation of spreading colonies on agar, and the porV mutant exhibited gliding motility and

66 i in tissue culture plates, colonies in soft agar, and tumors in nude mice.

67 colony of Escherichia coli growing on solid agar, and we develop a quantitative understanding by spa

68 e model of bacterial diffusion and growth in agar, are compared with our experimental measurements of

69 clay systems was analyzed using skimmed milk agar as food simulant and the largest inhibition zones w

70 the illumigene assay using culture on blood agar as the "gold standard" and following discrepancy an

71 slime; and (4) the comets etch trails in the agar as they move forwards.

72 Results obtained using a soft agar assay and shRNA Nrf2-transfected cells show that Nr

73 Transformation in a single layer soft agar assay could be documented as early as 2 to 3 days i

74 ndent cell growth ability was tested by soft agar assay following FA exposure.

75 In a soft agar assay, treatment of HC11-Int3 cells with P50-siRNA

76 ons and is strongly correlated with the soft-agar assay.

77 RCA1 dependent shown by 3D-matrigel and soft agar assays.

78 ckdown in a xenotransplant model and in soft agar assays.

79 l proliferation and colony formation in soft-agar assays.

80 was determined by colony formation and soft agar assays.

81 se activity in bacteria, producing a lighter agar background coloration facilitating visualization of

82 stem, and had been screened previously in an agar based system.

83 best practice would be concomitant use of an agar-based method and a Shiga toxin EIA, but a Shiga tox

84 i O157 infections will not be detected if an agar-based method is excluded from the enteric culture w

85 greement between broth macrodilution and the agar-based methods.

86 A brucella blood agar (BBA) plate, incubated anaerobically for 5 days, wa

87 RGM medium to Burkholderia cepacia selective agar (BCSA) and a standard acid-fast bacillus (AFB) cult

88 incubation on Burkholderia cepacia selective agar (BCSA) has been recommended as an expedient culture

89 The agar bead model of chronic P. aeruginosa lung infection

90 We have developed an adapted agar bead murine model using a clinical mucoid strain th

91 rotease and chitinase enzymes immobilized on agar beads.

92 ed to glycerol>lecithin>alginate, whereas 1% agar behaved differently, increasing all rheological val

93 id chromatography-mass spectrometry and disk agar biocidal diffusion tests indicate that the electroc

94 rain was defective for motility in semisolid agar, biofilm formation, and fluorescence on calcofluor

95 le-colony selection on antibiotic-containing agar, blinded to sequencing results.

96 eep blood chocolate agar, Sabouraud dextrose agar, brain heart infusion, thioglycolate broth, and Rob

97 ine MICs determined using 7H10 agar and 7H11 agar but not for bedaquiline MICs determined using 7H9 b

98 ating negative and "nonnegative" chromogenic agar can reduce the labor cost of these screens and pote

99 mation, anchorage-independent growth in soft agar, cell migration, and epithelial-mesenchymal transit

100 ng sterile swabs and inoculated on MacConkey agar, Chocolate agar and Blood agar culture Medias.

101 onventional media and into chromID CPS Elite agar (chromID).

102 The soft agar clonogenic assay showed that T80/KLF8 cells formed

103 activity attenuates cell proliferation, soft-agar colony formation and orthotopic GBM growth in NOD/S

104 ot CRAF WT, transformed NIH3T3 cells in soft-agar colony formation assays, increased kinase activity

105 hemical inhibition of Gln uptake blocks soft agar colony formation by Hace1(-/-) MEFs.

106 tion) signaling, transwell invasion and soft agar colony formation, and in vivo promoted lung metasta

107 n of CDH10 promoted cell proliferation, soft-agar colony formation, cell migration and cell invasion,

108 led to decreased transwell invasion and soft agar colony formation, without affecting proliferation.

109 cement of cell proliferation, increased soft agar colony size, and elevated ERK1/2 phosphorylation we

110 nd completely blocks their invasive and soft agar colony-forming abilities, but it spares nontransfor

111 erol compared with those of potato puree and agar, consequently affecting the rheological properties

112 ing brain heart infusion broth and MacConkey agar containing 1 mug/ml or 10 mug/ml of ciprofloxacin.

113 on woody biomass and is commonly studied on agar-containing medium which mimics its natural environm

114 tected that the mycelial growth on the solid agar created multiple surface and subsurface wrinkles wi

115 The divots in the agar, created by the high-pressure gas and spray, dramat

116 th SMAC agar culture and EIA, 6 (9%) by SMAC agar culture alone, and 2 (3%) by EIA alone.

117 lates, 57 (88%) were identified by both SMAC agar culture and EIA, 6 (9%) by SMAC agar culture alone,

118 on MacConkey agar, Chocolate agar and Blood agar culture Medias.

119 ngers siderophores were imaged directly from agar culture of S. wadayamensis, and well resolved and i

120 care center, i.e., sorbitol-MacConkey (SMAC) agar culture, enzyme immunoassay (EIA) for Shiga toxin,

121 ngs in 25 (89%) of the 28 sorbitol-MacConkey agar culture-negative STEC cases.

122 tely sort positive from negative chromogenic agar cultures regardless of the pigmentation produced.

123 ws direct mass spectrometry imaging (IMS) of agar cultures.

124 tted for exposure to UVA through 5 different agar depths (100 cell measurements/depth) and analyzed u

125 Different agars designed for the isolation of B. cepacia complex v

126 extracts was evaluated by broth-dilution and agar diffusion assay.

127 eluates against Streptococcus mutans through agar diffusion assays.

128 microdilution (BMD), macrodilution (MD), and agar dilution (AD) methods were compared.

129 Agar dilution and broth microdilution methods were evalu

130 ole at 16 mg/L in an enriched Brucella blood agar dilution assay.

131 ent Amendments (CLIA)-approved CLSI standard agar dilution method and, separately, by the Etest accor

132 The Etest and agar dilution methods were well correlated.

133 For the agar dilution MIC, a 4-dilution QC range (0.015 to 0.12

134 : 0.015 to 0.12 mug/ml for the 7H10 and 7H11 agar dilution MICs and 0.015 to 0.06 mug/ml for the 7H9

135 esults produced slightly lower MICs than the agar dilution results.

136 sults of the assay were 100% concordant with agar dilution susceptibility test results for 100 clinic

137 onorrhoeae ATCC 49226 control strain for MIC agar dilution testing (AD) and zones by disk diffusion t

138 can be effectively used as an alternative to agar dilution testing to determine the susceptibility of

139 rsity of Washington and CDC for confirmatory agar dilution testing; sequence data were sent to CDC fo

140 r the Etest can be used as an alternative to agar dilution to determine antimicrobial susceptibilitie

141 likely allow for successful transition from agar dilution to the Etest.

142 ution tests (two broth microdilution and two agar dilution) was achieved in only 76/114 (67%) of E. c

143 ere tested for colistin susceptibility using agar dilution, and characterised by whole genome sequenc

144 animal isolates were determined in vitro by agar dilution, biofilm formation, adhesion, invasion and

145 5 had ceftriaxone MICs = 0.125 microg/mL by agar dilution.

146 broth microdilution and that to carbadox by agar dilution.

147 ound the geometric mean included 95.8% (7H10 agar dilution; 204/213 observations with one data set ex

148 s with one data set excluded) or 95.9% (7H11 agar dilution; 232/242) of bedaquiline MICs.

149 ies were tested against 4 bacteria b y using agar disc diffusion and tube dilution tests.

150 dant, by MTT, nitric oxide inhibitory assay, agar disc diffusion method, and DPPH and ABTS assays.

151 robial effects by DPPH, ABTS, FRAP, ORAC and agar disc diffusion methods, respectively.

152 Antimicrobial activity was evaluated by the agar disk diffusion method, and in vitro cytotoxic activ

153 er growth on buffered charcoal yeast extract agar during the initial isolation and/or subcultures tha

154 Five chromogenic agars, evaluated using 400 stool specimens, were found t

155 ted keratitis, were cultured on non-nutrient agar examined by microscope for the presence of free-liv

156 Seaweed (Gracilaria fisheri) protein after agar extraction was hydrolysed using bromelain (enzyme a

157 upport iron acquisition on unsupplemented LB agar, Feo, Fbp, Vct, and Vib, remains functional.

158 aques, or holes, in a lawn of bacteria on an agar-filled Petri dish; however, this rate-limiting step

159 We characterized PIRL crater size using agar films containing Rhodamine.

160 riolus versicolor, pre-grown on kenaf/lignin agar followed by either vacuum evaporation or acid preci

161 cobacteria [RGM] medium and Middlebrook 7H11 agar), for their abilities to isolate NTM.

162 superior option, compared to other selective agars, for the isolation of rapidly growing mycobacteria

163 e cells when trypsinized and regrown in soft agar, formed colonospheres/organoids that developed into

164 Using MH agar from BD and Oxoid, susceptibility rates determined

165 With the disk diffusion method using MH agar from BD and Oxoid, susceptibility rates were 82.2%

166 ICV in hemagglutination inhibition (HI) and agar gel immunodiffusion assays, and inability to produc

167 Short-term release into an agar gel was evaluated using a fluorescent tracer (fluor

168 well as from a living bacterial colony on an agar gel.

169 s was followed by standard samples for blood agar, Gram stain, Sabouraud agar, thioglycolate broth, a

170 s necessary for its ability to increase soft agar growth and in vivo metastasis in an immunocompetent

171 ZNF322A promoted cell proliferation and soft agar growth by prolonging cell cycle in S phase in multi

172 high as 300 KPa on the surface of a standard agar growth medium.

173 naling pathways regulate proliferation, soft agar growth, and invasion of human lung adenocarcinoma c

174 snitzii strain 16-6-I 40 fastidious anaerobe agar had the greatest effect.

175 ms of localized corrosion in soil, semisolid agar has been developed as an analogue for soil.

176 g the colony expansion of cells deposited on agar have shown that the expansion rate increases with i

177 MSSA strains with strong blood agar hemolysis and high alpha-hemolysin activity are mar

178 agar with gentamicin (SDA), inhibitory mold agar (IMA), and brain heart infusion (BHI) agar with chl

179 sensor bacteria either in liquid culture or agar-immobilized, respectively, at a distance of 50 m in

180 aping was inoculated onto Sabouraud Dextrose Agar in C-shaped streaks and incubated at 25 degrees C a

181 se VAT failed to stimulate growth in soft of agar in cells deficient in FGFR-1 (FGF2 receptor).

182 ls enhanced proliferation and growth in soft agar in vitro but was insufficient to drive tumorigenesi

183 d the ability of these cells to grow in soft agar in vitro.

184 colistin-nalidixic acid (CNA), and MacConkey agars in 5% CO2 for 48 h.

185 ity testing was done in selected isolates by agar incorporation, and we used sequence data to determi

186 ard urine culture inoculated at 1 mul onto 2 agars incubated aerobically; expanded-spectrum EQUC inoc

187 MRSASelect II agar is a simple, rapid, and robust method to routinely

188 robiology laboratory; the use of chromogenic agar is one method by which the laboratory might expedit

189 Colony formation in soft agar is the gold-standard assay for cellular transformat

190 root skewing, an inability to penetrate hard agar layers, and abnormal growth responses to impenetrab

191 s unable to tumble become trapped within the agar matrix.

192 at in low-prevalence settings, CPE screening agars may lack specificity, and confirmation of putative

193 s of Chlamydomonas strains by propagation on agar media and by cryogenic storage, (2) identify mutage

194 ct analysis of microbial cocultures grown on agar media by desorption electrospray ionization mass sp

195 bers were determined by culture on selective agar media or by epifluorescence microscopy.

196 performed using a liquid medium and a solid agar medium with an incubation period of up to 60 days.

197 ed, homogenized, and cultured in tryptic soy agar medium.

198 ureus genome that altered hemolysis on blood agar medium.

199 bles had a minimal effect on gepotidacin pH, agar method, atmospheric condition, temperature, and add

200 routine AST media, including Mueller-Hinton agar (MHA) and cation-adjusted Mueller-Hinton broth.

201 growing cells of Escherichia coli in curved agar microchambers, and find that chemoreceptor cluster

202 gene responsible for halo production on LBC agar, named choA, was identified as an N-acyltransferase

203 phorylated ERK, and slows the growth in soft agar of HCT116 cells.

204 obese human donors stimulated growth in soft agar of non-tumorigenic epithelial cells.

205 iety of substrates including potato dextrose agar, olive oil, glyceride trioleate, oleic acid and the

206 se and inoculated on enriched Brucella blood agar, on which were placed identical lengths of surgical

207 ine MICs determined using 7H9 broth and 7H10 agar or 7H9 broth and 7H11 agar.

208 methods developed in the mid-1800s-growth on agar or in broth-identification and susceptibility profi

209 ability of C6 cells to form colonies in soft agar or spheres when grown in suspension.

210 atment group was inoculated onto nonnutrient agar overlaid with Enterobacter aerogenes.

211 actinomycetemcomitans was examined using the agar overlay technique and agar well diffusion method.

212 al cultures from multiwell plates onto large agar pads using inexpensive replicator pins and automati

213 g: 100 mul of urine plated onto blood (blood agar plate [BAP]), colistin-nalidixic acid (CNA), and Ma

214 The fibrin agar plate assay further confirmed the thrombin-mediated

215 Early semiquantitative sputum agar plate culture results can be used to predict sympto

216 We compared the Remel Spectra CRE agar plate to CDC standard methodology for the isolation

217 of meropenem and subcultured to a MacConkey agar plate with a 10-mug meropenem disk) and for sequenc

218 ith height variations up to 0.8 mm above the agar plate.

219 were performed from growth on BMHA and blood agar plates (BAP), with and without cefoxitin disk induc

220 lagellated counterparts in spreading on soft-agar plates and through medium-filled channels despite h

221 on Module (CDM) for categorizing chromogenic agar plates as negative or "nonnegative" for vancomycin-

222 Remel Spectra CRE agar plates can provide useful means for a fast and reli

223 st area, and assistant's chest area on blood agar plates in all three groups.

224 Head-to-head competition assays on agar plates indicate that two-dimensional constraint on

225 ssor tRNA yielded transformants that grow on agar plates lacking uracil.

226 Agar plates of fungi present a complex topography due to

227 rabidopsis thaliana) seedlings were grown on agar plates under different salt stress conditions.

228 The blood agar plates were incubated at 37 degrees C for 48 hours,

229 ies of a 6PGDH mutant library growing on the agar plates were treated by heat to minimize the backgro

230 f metabolites in tissues, cell cultures, and agar plates with cellular resolution, but it is hampered

231 When grown in agar plates with reduced iron concentration, triple bhlh

232 orm multicellular patterns as they expand on agar plates, a phenotype that requires a functional copy

233 confirmed by culturing samples overnight on agar plates, followed by a microscopic examination.

234 On agar plates, red colonies are simply visualized in ambie

235 ing Bacillus subtilis ATCC 49760 colonies on agar plates.

236 Overexpression of bsrE causes cell lysis on agar plates.

237 at cultures on selective streptococcal blood agar plates.

238 H. glycines J2 and Caenorhabditis elegans on agar plates.

239 found arising from the edges of colonies on agar plates.

240 from positive blood cultures using prewarmed agar plates.

241 (AST) systems and five selective chromogenic agar plates.

242 ed in stronger seedling growth inhibition on agar plates.

243 ed on two different types of VRE chromogenic agar plates.

244 Polymyxins diffuse poorly into agar, potentially giving inaccurate disk diffusion and E

245 linical MRSA isolates were grown on nutrient agar, prepared in suspension, and adjusted to concentrat

246 aria gracilis and O. pinnatifida were mostly agar producers.

247 om archival type specimens of ten species in agar-producing red algal genera Gelidium and Pterocladie

248 mycin (STR), overall concordance between the agar proportion method and microarray analysis was 89.5%

249 susceptibility testing (DST) by the indirect agar proportion method for a panel of first-line and sec

250 A novel selective agar (RGM medium) has been advocated for the isolation o

251 (5% sheep blood agar, sheep blood chocolate agar, Sabouraud dextrose agar, brain heart infusion, thi

252 ins) and culture examination (5% sheep blood agar, sheep blood chocolate agar, Sabouraud dextrose aga

253 including impaired colony formation in soft agar, spheroid formation, and xenograft growth.

254 n a dose-dependent manner when applied on an agar substrate.

255 damide is capable of producing a halo on LBC agar suggesting that this molecule is solubilizing the c

256 sed in Escherichia coli, produce halos on LB agar supplemented with 0.01% (w/v) cholesterol (LBC agar

257 iously, we showed that Pseudomonas isolation agar supplemented with ammonium metavanadate (PIAAMV) in

258 ed in a series of IMC ampoules with nutrient agar supplemented with increasing concentrations of amox

259 BHI agars supplemented with vancomycin 4 (BHI-V4) and 3 (BHI

260 that populations confined to grow on a flat agar surface are more susceptible than their well-mixed

261 (PHE) to a model soil-atmosphere interface (agar surface) in the presence and absence of glass fiber

262 FLO11 gene constrains cells to grow near the agar surface, causing the formation of larger and more i

263 As a worm crawls on an agar surface, we found that substrate viscoelasticity in

264 ver FLO11 knockout (flo11Delta) cells on the agar surface.

265 is the formation of a shallow groove on the agar surface.

266 ans undulatory motions on a wet viscoelastic agar surface.

267 he budding yeast Saccharomyces cerevisiae on agar surfaces as a model for mutualists undergoing spati

268 ofilms were developed anaerobically on blood agar surfaces in 96-well plates using a growth medium of

269 own that S. aureus can passively move across agar surfaces in a process called spreading.

270 al twisting instead of waving on tilted hard-agar surfaces.

271 Isolates were grown on Sabouraud-Dextrose agar, swabbed, and prepared in suspension, and 1 mL aliq

272 a swab with an anaerobic transport semisolid agar system for their capacities to maintain the viabili

273 ificantly fewer and smaller colonies in soft agar than their 2D-irradiated counterparts (gamma P = 0.

274 io alginolyticus isolate B522 on carrageenan agar that may lay the foundation for swarming studies of

275 amples for blood agar, Gram stain, Sabouraud agar, thioglycolate broth, and brain heart infusion brot

276 mm settle plates containing potato dextrose agar to the air for 10 min.

277 results between disk manufacturers and some agar types and also with potassium and thymidine for S.

278 Chromogenic agar used at these sites included MRSASelect (Bio-Rad La

279 sm identification was decreased with chromID agar versus conventional media for E. coli (mean of 24.4

280 liquid and embedded in glucose-limited soft agar, we evaluate the fit of this model to experimental

281 Using Leptospira Vanaporn Wuthiekanun (LVW) agar, we maintained 100 pathogenic Leptospira isolates f

282 xamined using the agar overlay technique and agar well diffusion method.

283 In the agar well diffusion tests, zones of inhibition for the d

284 inst test microorganisms was assessed by the agar well-diffusion method.

285 ically in hemolysis or growth on human blood agar were identified by comparing the mutants to the par

286 nts HeLa cells from forming colonies in soft agar, when paxillin is knocked down together with Cat-1,

287 motes their ability to form colonies in soft agar, whereas ectopically expressing paxillin in these c

288 nes to proliferate and form colonies in soft agar, whereas EWSAT1 inhibition had no effect on other c

289 hrough collagen and decreased growth in soft agar, whereas the second was enriched in cells with an e

290 e on anaerobic colistin nalidixic acid (CNA) agar which likely facilitated its detection and identifi

291 axis response, migration in classic motility agar, which constitutes a fluid-filled porous medium, is

292 ple sample dehydration leads to a thin solid agar, which enables the direct use of spray-based ambien

293 e in the order of glycerol>alginate>lecithin>agar, while at 1% concentration, the order changed to gl

294 ntially used to inoculate BBL Trypticase soy agar with 5% sheep blood (TSA II) and each chromogenic m

295 ion, invasion, and colony formation, in soft agar with CD66(high) cells.

296 d agar (IMA), and brain heart infusion (BHI) agar with chloramphenicol and gentamicin.

297 culture media, including Sabouraud dextrose agar with gentamicin (SDA), inhibitory mold agar (IMA),

298 (range, 89.9 to 93.9%) to bile esculin azide agar with vancomycin (BEAV) agar (84.8%) for detecting v

299 sults were similar using the three different agars with a sensitivity of 100% and specificity ranging

300 e, sulphated galactose and the gelling agent agar, with the sulphate content estimated as 51.01 mug/m