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Sample GSM578567 Query DataSets for GSM578567
Status Public on Aug 31, 2013
Title SLEC-CST0-Ba90-Liver-01
Sample type RNA
 
Source name early stage compstatin treated animal's liver
Organism Papio cynocephalus
Characteristics tissue: Liver
stress: E.coli (serotype B7-086a:K61) challenge
agent: compstatin
sepsis stage: early stage
protocol: prevention regimen
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 early stage compstatin treated 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 274.873889
1053_at 26.323859
117_at 29.267948
121_at 363.340648
1255_g_at 15.384817
1294_at 113.455543
1316_at 49.687757
1320_at 45.29141
1405_i_at 29.219297
1431_at 2683.078157
1438_at 66.85828
1487_at 311.724507
1494_f_at 2188.897577
1598_g_at 329.72236
160020_at 187.926815
1729_at 219.550143
1773_at 52.926212
177_at 25.294891
179_at 414.890256
1861_at 72.976725

Total number of rows: 22277

Table truncated, full table size 462 Kbytes.




Supplementary file Size Download File type/resource
GSM578567.CEL.gz 2.0 Mb (ftp)(http) CEL
Processed data included within Sample table

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