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Sample GSM93656 Query DataSets for GSM93656
Status Public on Feb 15, 2006
Title Ad infected murine liver-MO30k-(229)-6hpi
Sample type RNA
 
Channel 1
Source name Cy5 labeled Liver RNA
Organism Mus musculus
Characteristics C57/BL6 C3KO murine Liver RNA- 6 hours post-injection with a 1st generation (E1-E3-CMVLacZ) vector.
Biomaterial provider Amalfitano Lab
Treatment protocol The RNA (10 µg) was a total RNA mix that was assessed for quality with an Agilent Lab-on-a-Chip 2100 Bioanalyzer (Agilent Technologies, Palo Alto, USA).
Extracted molecule total RNA
Extraction protocol RNA isolation was accomplished by homogenizing liver in liquid nitrogen, then extracting RNA using TriReagent (Molecular Research Center, Inc.). The RNA (10 µg) was purified using an RNeasy Kit (Qiagen) and assessed for quality with an Agilent Lab-on-a-Chip 2100 Bioanalyzer (Agilent Technologies, Palo Alto, USA).
Label Cy5
Label protocol The RNA from murine liver was directly labeled with Cy dyes using oligo dT primers, for complete details see http://mgm.duke.edu/genome/dna_micro/core/protocols/ for detailed labeling and hybridization protocols
 
Channel 2
Source name Murine Reference RNA
Organism Mus musculus
Characteristics Murine Universal RNA (Stratagene, La Jolla, CA) which is a mixture of RNA from 10 control cell lines approximating the expression profile of the majority of murine genes was used.
Biomaterial provider Stratagene
Treatment protocol The RNA (10 µg) was a total RNA mix that was assessed for quality with an Agilent Lab-on-a-Chip 2100 Bioanalyzer (Agilent Technologies, Palo Alto, USA).
Extracted molecule total RNA
Label Cy3
Label protocol The RNA from murine liver was directly labeled with Cy dyes using oligo dT primers, for complete details see http://mgm.duke.edu/genome/dna_micro/core/protocols/ for detailed labeling and hybridization protocols
 
 
Hybridization protocol Hybridization of a Cy labeled cDNA probe (mix of Cy3 and Cy5) onto coated slide spotted with oligonucleotides (70mers) was performed as described in detail at http://mgm.duke.edu/genome/dna_micro/core/protocols/SOP_hyb.doc.
Scan protocol Fluorescent array images were collected for both Cy3 and Cy5 with a Axon GenePix Pro 4000A scanner and image intensity data were extracted and analyzed with Microarray Analysis Suite (MAS) 5.0 software.
Description Sample is C57/Bl6 C3KO liver RNA extract after infected with 1st generation LacZ adenovirus (1.5x10E11 particles per mouse) at 6 hpi.
Data processing VALUE column is the log2 ratio of normalized Cy5:Cy3 signal after Intensity-Dependent normalization.
 
Submission date Jan 24, 2006
Last update date Jan 31, 2006
Contact name Zachary Conrad Hartman
E-mail(s) zch@duke.edu
Phone 919-684-9197
Organization name Duke University
Department Surgery
Lab Lyerly Lab
Street address Research Drive MSRB rm 414
City Durham
State/province NC
ZIP/Postal code 27710
Country USA
 
Platform ID GPL3222
Series (1)
GSE4128 Ad vectors in C3KO mice

Data table header descriptions
ID_REF
VALUE Log2 of normalized Cy5/Cy3 values
PRE_VALUE Ratio of normalized Cy5/Cy3 values
Control Control Signal from Reference RNA
Raw Raw signal from Labeled RNA
FLAGS P denotes satisfactory features

Data table
ID_REF VALUE PRE_VALUE Control Raw FLAGS
M200000001 -0.621488377 0.65 12.35 8 P
M200000002 -5.058893689 0.03 1625 49 P
M200000004 -0.577766999 0.67 137.7 92 P
M200000005
M200000006 0.070389328 1.05 174 182 P
M200000007
M200000008
M200000009 -0.810966176 0.57 297.5 168 P
M200000010 -0.304006187 0.81 22.37 18 P
M200000011 0.516015147 1.43 21 30 P
M200000012 -0.340075442 0.79 100.6 79 P
M200000014
M200000016 0.250961574 1.19 52.92 63 P
M200000017 -0.862496476 0.55 30.77 17 P
M200000019
M200000020 -1.321928095 0.4 14.93 6 P
M200000021
M200000023 -1.395928676 0.38 65.51 25 P
M200000025
M200000027

Total number of rows: 31780

Table truncated, full table size 780 Kbytes.




Supplementary data files not provided

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