ライフサイエンスコーパス: agar media

1 and P. aeruginosa colonies on commonly used agar media.

2 designed to lyse cells grown in colonies on agar media.

3 uid media or hyperelongated swarmer cells on agar media.

4 iffusion tests, and Etests, on six different agar media.

5 containing hlyA was beta-hemolytic on blood agar media.

6 oculated into selective broth and onto blood agar media.

7 ate colonies with extensive hyphal growth on agar media.

8 other method for lowering water potential of agar media.

9 d media, including LB agar and King's B (KB) agar media.

10 s, were impaired for growth on iron-depleted agar media.

11 ore formation) can be seen on the surface of agar media.

12 ing on a tilted surface of impenetrable hard-agar media adopt a wave-like pattern and tend to skew to

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

14 ve (fad) genes, produced smaller colonies on agar media, and grew slower in rich broth than did the w

15 levels in the roots of young plants grown on agar media, and that the expression level is greatly ind

16 treatments to reduce the water potential of agar media, and thus induce drought conditions in the la

17 While EPS66A did not directly inhibit Xaj on agar media, applying it at 200 mug/mL, 24 h after Xaj in

18 333 swabs was cultured on several selective agar media before and after broth enrichment.

19 e prototype strips were evaluated on several agar media (brain heart infusion agar, Isosensitest agar

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

21 nd Gram-positive clinical isolates) grown on agar media by liquid extraction surface analysis mass sp

22 idious and the selection of mutants on solid agar media can take up to 6 weeks.

23 eight agar media, including four sheep blood agar media: chocolate agar, brain heart infusion blood a

24 h 10 microM FB1 and seedlings transferred to agar media containing 1 microM FB1 develop lesions remin

25 ective hyphal formation when placed on solid agar media, either in response to nutrient deprivation o

26 served when grown on the surface of nutrient agar media, facilitating analysis of responses to stimul

27 cultures of Bacillus globigii (BG) grown on agar media for 4 days or longer.

28 genes that are not expressed on traditional agar media, identify subtle interactions between P. pate

29 Isolator sediment was divided among eight agar media, including four sheep blood agar media: choco

30 beta-hemolysis surrounding colonies on blood-agar media is a hallmark phenotypic feature of the patho

31 axial twisting, and root growth on inclined agar media is strongly right skewed.

32 The Rv1170 mutant grew poorly on agar media lacking catalase and oleic acid, and had heig

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

34 an acidic pH of 6.0 instead of the usual for agar media, pH 6.8, to provide optimal conditions for PZ

35 of diploid budding yeast onto nitrogen-poor agar media stimulates a MAPK pathway to promote filament

36 tion of this organism in tryptone-based soft agar media supplemented with different salts.

37 sures growth of Aspergillus species on solid agar media that contain serial dilutions of caspofungin

38 Overall, oatmeal cereal and rice agar media were comparable in their abilities to support

39 Growth characteristics on various agar media were compared.

40 tup1Delta strain failed to form colonies on agar media while inocula of 10(5)-10(6) cells per plate

41 arine bacteria Pseudoalteromonas on nutrient agar media without any sample preparation.