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Status |
Public on Dec 18, 2014 |
Title |
E. coli in supernatant from B. theta_OD=0.5_rep.2 |
Sample type |
RNA |
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Source name |
Escherichia coli O103:H25 in supernatant at OD=0.5
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Organism |
Escherichia coli O103:H25 |
Characteristics |
co-culture/in supernatant/alone: in supernatant treated/not treated: not treated
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Growth protocol |
E. coli O103:H25 was grown individually or in co-culture with Bacteroides thetaiotaomicron to mid-log phase (OD 600nm 0.5) anaerobically in modified BHI media (Elay et al., J Med Microbiol. (1985), 19(2):195)
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Extracted molecule |
total RNA |
Extraction protocol |
Total RNA was extracted using a Purelink RNA mini kit (Life technologies, Carlsbad, California). DNA was removed using a Turbo DNA-free kit (Invitrogen). RNA quality and concentration was determined by analysis with an Agilent 2100 bioanalyzer.
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Label |
Cy3
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Label protocol |
For labeling of the cDNA samples, the NimbleGen protocol was followed.
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Hybridization protocol |
The hybridization of samples in randomized order to custom designed by NimbleGen arrays
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Scan protocol |
The samples were read with a GenePix 4000B scanner
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Description |
E. coli in supernatant from Bacteroides thetaiotaomicron at OD=0.5. It is the second of three biological replicates.
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Data processing |
RMA was used as the normalization algorithm in accordance with Nimblegen recommendation. Batch correction was performed with the ComBat function of the SVA package.
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Submission date |
Mar 08, 2013 |
Last update date |
Dec 19, 2014 |
Contact name |
Hildegunn Iversen |
E-mail(s) |
[email protected]
|
Phone |
004795147301
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Organization name |
Norwegian School of Veterinary Science
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Department |
Department of Food Safety and Infection Biology
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Lab |
Food Safety
|
Street address |
P.O.Box 8146 Dep
|
City |
Oslo |
ZIP/Postal code |
0033 |
Country |
Norway |
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Platform ID |
GPL16737 |
Series (1) |
GSE44790 |
Transcription analysis of E. coli O103:H25 in co-culture with Bacteroides thetaiotaomicron CCUG 10774 |
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