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Sample GSM578564 Query DataSets for GSM578564
Status Public on Aug 31, 2013
Title SLEC-Ba11-Liver-01
Sample type RNA
 
Source name E.coli challenged animal's liver
Organism Papio cynocephalus
Characteristics tissue: Liver
stress: E.coli (serotype B7-086a:K61) challenge
agent: untreated
sepsis stage: n/a
Treatment protocol Papio cyanocephalus baboons were held for 30 days at the OUHSC animal facility. Only healthy tuberculosis free animals with hemoglobin greater than 10 g/dL and white blood cell (WBC) count less than 12,000 were included in the study. Animals were infused with 1x109 live E. coli (LD50 dose) as described before. The time point at which the infusion was started is further indicated as T0, a time point of n hours thereafter referred to as T+n hours. Compstatin was administered as a 10-mg/kg iv. bolus followed by 60μg/kg/min continuous infusion. Three experimental E. coli groups were studied: (i) E. coli challenge only (n=4); (ii) E. coli plus compstatin treatment from T0 to T+8 (n=4; prevention regimen); (iii) E. coli plus compstatin from T+5 to T+11 (n=4; rescue regimen). The control group comprising three animals received saline infusion only.
Growth protocol Live E. coli organisms (serotype B7-086a:K61; American Type Culture Collection, Rockville, MD), stored in the lyophilized state at 4°C after growth in tryptic soybean agar, were reconstituted and used. To eliminate differences due to E. coli strain variations, all animals were infused with E. coli from this single isolate.
Extracted molecule total RNA
Extraction protocol Trizol extraction of total RNA was performed according to the manufacturer's instructions, RNA was further purified with the Qiagen DNeasyTissue kit (Qiagen, Valencia, CA) and the contaminant genomic DNA was removed with a Qiagen on-column DNase digestion kit. RNA concentrations are determined on a scanning UV/VIS spectrophotometer Nanodrop ND-1000 Spectrophotometer. RNA Quality Assessment by using Agilent 2100 Bioanalyzer Capillary Gel Electrophoresis System.
Label Biotin
Label protocol Biotinylated cRNA were prepared according to the standard Affymetrix protocol from 10 ug total RNA (Expression Analysis Technical Manual, 2001, Affymetrix).
 
Hybridization protocol Following fragmentation, 20 ug of cRNA were hybridized using Model 640 hybridization oven for 16 hr at 45C on GeneChip Human Genome Array U133A 2.0. GeneChips were washed and stained in the Affymetrix GeneChip® 450 fluidics station.
Scan protocol GeneChips were scanned using GeneChip® 3000 7G scanner with autoloader (0.51 micron resolution)
Description Gene expression data from E.coli challenged baboon liver
Data processing RMA
 
Submission date Aug 12, 2010
Last update date Aug 31, 2013
Contact name florea lupu
E-mail(s) [email protected]
Phone 405-271-7483
Fax 405-271-7417
Organization name Oklahoma Medical Research Foundation
Street address 825 NE 13th Street
City Oklahoma City
ZIP/Postal code 73104
Country USA
 
Platform ID GPL571
Series (1)
GSE23590 Gene expression data from compstatin treated E.coli-Induced primate sepsis model

Data table header descriptions
ID_REF
VALUE RMA signal intensity

Data table
ID_REF VALUE
1007_s_at 344.154178
1053_at 28.244494
117_at 27.841188
121_at 280.341798
1255_g_at 14.594638
1294_at 94.043066
1316_at 43.227287
1320_at 61.98235
1405_i_at 32.416347
1431_at 8846.593127
1438_at 61.701612
1487_at 307.355591
1494_f_at 2111.292181
1598_g_at 295.034605
160020_at 162.858689
1729_at 211.757553
1773_at 48.157353
177_at 27.718392
179_at 373.47427
1861_at 47.520972

Total number of rows: 22277

Table truncated, full table size 462 Kbytes.




Supplementary file Size Download File type/resource
GSM578564.CEL.gz 2.0 Mb (ftp)(http) CEL
Processed data included within Sample table

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