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Sample GSM451255 Query DataSets for GSM451255
Status Public on Mar 03, 2010
Title SWR-rep1d
Sample type RNA
 
Channel 1
Source name ovary, mouse, SWR
Organism Mus musculus
Characteristics strain: SWR
gender: female
tissue: ovary
age: 8 weeks old
Extracted molecule total RNA
Extraction protocol Total RNA was extracted with Trizol ® following manufacturer´s protocol
Label dUTP-Cy5
Label protocol 12 µg of total RNA were primed with 1 µg of random hexamers plus 1 µg of oligo-dT at 75°C for 10 min, then reversed transcribed at 42°C for 2.5 h with 500 U SuperScript II (Invitrogen), and 0.5 mM each dATP, dCTP, dGTP, 0.2 mM dTTP, and 0.1 mM dUTP-Cy3 (or Cy5, when corresponded).
 
Channel 2
Source name reference RNA
Organism Mus musculus
Characteristics strain: FVB
gender: male
tissue: whole organism
age: newborn
Extracted molecule total RNA
Extraction protocol Total RNA was extracted with Trizol ® following manufacturer´s protocol
Label dUTP-Cy3
Label protocol 12 µg of total RNA were primed with 1 µg of random hexamers plus 1 µg of oligo-dT at 75°C for 10 min, then reversed transcribed at 42°C for 2.5 h with 500 U SuperScript II (Invitrogen), and 0.5 mM each dATP, dCTP, dGTP, 0.2 mM dTTP, and 0.1 mM dUTP-Cy3 (or Cy5, when corresponded).
 
 
Hybridization protocol Labeled test and reference cDNAs were mixed with 35 µg of mouse Cot1 DNA, 35 µg of poli-dA in a solution containing 0.1% SDS and 3.5X SSC. Slides were place in closed hybridization chambers and incubated for 16-20 hrs in a water bath at 65°C. Washes in 2X SSC-0.1% SDS, 1X SSC, 0.2X SSC, and 0.05X SSC were performed sequentially, 1-min each.
Scan protocol Microarrays were quickly dried and scanned at 10-µm resolution in a ScanArray-Lite scanner (Perkin Elmer, MA). PMT was adjusted to obtain maximal signal intensities with minimal saturation
Description n/a
Data processing Microarray images were saved in TIFF format and extracted as GenePix result (gpr) files using GenePix Pro III software (Molecular Devices, CA). Data was subjected to print-tip (local) Loess normalization and scale adjustment with the DNMAD tool (http://dnmad.bioinfo.cnio.es) and then filtered/imputed for missing values with the preP tool (http://prep.bioinfo.cnio.es/).
 
Submission date Sep 09, 2009
Last update date Sep 09, 2009
Contact name Ulises Urzua
E-mail(s) uurzua@med.uchile.cl
Phone 56-2-29786877
Organization name University of Chile
Department Basic and Clinical Oncology
Lab Genomica Aplicada
Street address Independencia 1027
City Santiago
ZIP/Postal code 8380453
Country Chile
 
Platform ID GPL9169
Series (1)
GSE18045 Ovarian transcriptional profiles of four mouse strains

Data table header descriptions
ID_REF
VALUE lowess normalized log2 ratio representing test/reference (Cy5/Cy3 in direct, and Cy3/Cy5 in reverse experiments). The suffixes d and r in Sample names and matrix headers stand for direct and reverse experiments, respectively. Data from reverse experiments has been multiplied by (-1.0) in the matrix data spreadsheet.

Data table
ID_REF VALUE
C0001D10 0.107
C0001E04 0.973
C0003E09 0.327
C0003G10 0.47
C0004C11 0.051
C0004F03 0.622
C0005A12 -0.306
C0005C09 0.121
C0005G04 0.735
C0005G12 0.134
C0006B07 0.367
C0006D09 -0.26
C0007D02 -0.148
C0007D12 -0.086
C0007G04 0.329
C0007G09 -0.142
C0008H11 0.102
C0009D02 0.303
C0009D08 0.043
C0009E06 -0.091

Total number of rows: 14586

Table truncated, full table size 219 Kbytes.




Supplementary file Size Download File type/resource
GSM451255_MmNIA_102p4_madbID42739.gpr.gz 1.3 Mb (ftp)(http) GPR
Processed data included within Sample table

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