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Sample GSM451241 Query DataSets for GSM451241
Status Public on Mar 03, 2010
Title BalbC-rep4r
Sample type RNA
 
Channel 1
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-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 ovary, mouse, BalbC
Organism Mus musculus
Characteristics strain: BalbC
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-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 0.272
C0001E04 0.675
C0003E09 0.14
C0003G10 0.806
C0004C11 0.023
C0004F03 -0.029
C0005A12 -0.285
C0005C09 0.585
C0005G04 -0.318
C0005G12 0.906
C0006B07 0.168
C0006D09 0.432
C0007D02 0.858
C0007D12 0.67
C0007G04 0.311
C0007G09 0.603
C0008H11 -0.485
C0009D02 0.298
C0009D08 0.121
C0009E06 0.454

Total number of rows: 14586

Table truncated, full table size 219 Kbytes.




Supplementary file Size Download File type/resource
GSM451241_MmNIA_80p2_madbID31677.gpr.gz 1.1 Mb (ftp)(http) GPR
Processed data included within Sample table

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