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Sample GSM388213 Query DataSets for GSM388213
Status Public on Apr 15, 2009
Title MDA-MB-231 genomic DNA
Sample type genomic
 
Channel 1
Source name healthy female donors
Organism Homo sapiens
Characteristics sample type: reference (pooled genomic DNA)
gender: female
Growth protocol Cell cultures were grown to 70-80% confluence in 175 cm2 flasks according to distributor's instructions (ATCC).
Extracted molecule genomic DNA
Extraction protocol Genomic DNA was extracted from untreated cells using the NucleoSpin Tissue kit with the protocol for cultured cells.
Label Cy3
Label protocol Six micrograms of digested and purified tumour and reference DNA was labelled with Cy5-dUTP and Cy3-dUTP, respectively, in a random priming reaction using BioPrime DNA Labelling System.
 
Channel 2
Source name breast cancer cell line MDA-MB-231
Organism Homo sapiens
Characteristics sample type: test
cell line: MDA-MB-231 breast cancer cell line
Growth protocol Cell cultures were grown to 70-80% confluence in 175 cm2 flasks according to distributor's instructions (ATCC).
Extracted molecule genomic DNA
Extraction protocol Genomic DNA was extracted from untreated cells using the NucleoSpin Tissue kit with the protocol for cultured cells.
Label Cy5
Label protocol Six micrograms of digested and purified tumour and reference DNA was labelled with Cy5-dUTP and Cy3-dUTP, respectively, in a random priming reaction using BioPrime DNA Labelling System.
 
 
Hybridization protocol Labelled tumor and reference samples were combined and hybridized onto the arrays according to manufacturer's (Agilent) instructions. After hybridization, arrays were washed according to manufacturer's instructions.
Scan protocol Arrays were scanned using the G2565 scanner from Agilent Technologies. Signal intensities were quantified using the Feature Extraction software version 7.5.1 from Agilent.
Description no additional information
Data processing Agilent Feature Extraction Software (v 7.5.1) was used for spot quality filtering and normalization.
 
Submission date Mar 31, 2009
Last update date Apr 01, 2009
Contact name Henrik Edgren
E-mail(s) [email protected]
Organization name Institute for Molecular Medicine, University of Helsinki
Street address Tukholmankatu 8
City Helsinki
ZIP/Postal code 00290
Country Finland
 
Platform ID GPL8355
Series (1)
GSE15477 Data integration from two microarray platforms identifies genetic inactivation of RIC8A in a breast cancer cell line

Data table header descriptions
ID_REF
VALUE normalized log10 ratio Cy5/Cy3

Data table
ID_REF VALUE
1 -1.524143244e+000
2 0.000000000e+000
3 2.610139172e-002
4 6.831247408e-002
5 -2.413203708e-001
6 -3.861096002e-002
7 -1.481354214e+000
8 -5.437040198e-002
9 1.699441597e-002
10 1.475631355e-002
11 -1.173692647e-001
12 2.431264632e-001
13 -1.330384628e-001
14 -1.535469949e+000
15 2.148974587e-001
16 -7.502645203e-002
17 1.720648847e-001
18 -1.531741561e-001
19 5.471650947e-002
20 3.896095980e-001

Total number of rows: 42603

Table truncated, full table size 968 Kbytes.




Supplementary file Size Download File type/resource
GSM388213.txt.gz 9.7 Mb (ftp)(http) TXT
Processed data included within Sample table

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