|
Status |
Public on Sep 30, 2018 |
Title |
Wild type, rep 1 |
Sample type |
RNA |
|
|
Source name |
Pseudomonas aeruginosa airway infection
|
Organism |
Pseudomonas aeruginosa |
Characteristics |
host strain: C57BL/6 host strain gener: female infection tissue: mouse lung bacteria infection: P. aeruginosa in vivo infection time point: 24 h post-infection
|
Treatment protocol |
Infected animals as described above were euthanized 24 h post-infection.
|
Growth protocol |
P.aeruginosa strains were grown in LB at 37°C overnight.
|
Extracted molecule |
total RNA |
Extraction protocol |
RNA was isolated from airway homogenate pellets using Trizol according to the manufacturer's instructions. Samples were treated with DNAse, then rRNA was removed from 1 to 5 μg of total RNA using the RiboZero kit for Gram-negative bacteria. rRNA-depleted samples were concentrated by EtOH precipitation. cDNA synthesis and hybridization to Affymetrix GeneChip P. aeruginosa genome arrays.
|
Label |
biotin
|
Label protocol |
Biotinylated cRNA were prepared according to the standard Affymetrix protocol from total RNA
|
|
|
Hybridization protocol |
Following fragmentation, cRNA were hybridized on GeneChip P. aeruginosa Genome Array. GeneChips were washed and stained in the Affymetrix Fluidics Station 450.
|
Scan protocol |
GeneChip 3000 7G scanner
|
Description |
WT_1
|
Data processing |
Biomedical Genomics Workbench 4
|
|
|
Submission date |
Feb 05, 2018 |
Last update date |
Sep 30, 2018 |
Contact name |
Shi-qi An |
Organization name |
Queen's University Belfast
|
Street address |
Lisburn Road
|
City |
Belfast |
ZIP/Postal code |
UK BT9 7BL |
Country |
United Kingdom |
|
|
Platform ID |
GPL84 |
Series (1) |
GSE110126 |
The impact of DSF and C23 on P. aeruginosa physiology |
|