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Sample GSM1092253 Query DataSets for GSM1092253
Status Public on Jul 12, 2013
Title MCF7_day3_expression
Sample type RNA
 
Source name MCF7 breast cancer cell line, day 3
Organism Homo sapiens
Characteristics gender: Female
disease: Breast cancer
er: +
Growth protocol Cells were grown for three days changing media every day
Extracted molecule total RNA
Extraction protocol Total RNA was isolated using TriZol (Invitrogen) followed by RNeasy Mini Kit (Qiagen) according to manufacturers’ manuals. RNA quality was assessed by Nanodrop-1000 spectrometer for OD260/280 and OD260/230 ratio and Bioanalyzer (Agilent Technologies).
Label Cy3
Label protocol 400 ng total RNA was amplified and labeled using the Low RNA Input Fluorescent Linear Amplification Kit (Cat# 5190-0447, Agilent Technologies) with oligo dT primers (Cat# RA300A-2, System Bioscience) and cyanine-labeled CTPs (Perkin Elmer) according to manufacturer’s manual. Labeled cRNA was purified using RNeasy Mini Kit (Qiagen). RNA spike-in controls (Agilent Technologies) were added to RNA samples before amplification and labeling according to manufacturer’s protocol.
 
Hybridization protocol 825 ng of labeled RNA was fragmented, denatured and hybridized to the array at 60ºC for 17 hours in a hybridization oven with rotation. After hybridization, arrays were washed and dried according to the Agilent microarray processing protocol.
Scan protocol Arrays were scanned by Agilent G2505C Scanner controlled by Agilent Scan Control 7.0 Software. Data were extracted with Agilent Feature Extraction Software.
Description MCF7_day3
jhu_251485070373_S01_GE2_107_Sep09_1_2_MCF7 Mock Day3 RNA-Cy3_MCF7 AZA Day3 RNA_Cy5
Data processing Raw median foreground signals were taken for both channels. LOESS normalization for within-array normalization, and A-quantile normalization for between-arrays normalization were performed using R and Bioconductor. 2-channel arrays were analyzed as single-channel. The second color is not analyzed in this analysis.
 
Submission date Mar 04, 2013
Last update date Jul 12, 2013
Contact name Francescopaolo Di Cello
E-mail(s) fdicello@hotmail.com
Organization name The Johns Hopkin University School of Medicine
Street address 1650 Orleans Street
City Baltimore
State/province MD
ZIP/Postal code 21287
Country USA
 
Platform ID GPL6480
Series (2)
GSE44836 Gene expression profile of breast cancer cells.
GSE44838 Gene expression and methylation profile of breast cancer cells.

Data table header descriptions
ID_REF
VALUE Normalized Cy3 or Cy5 signal.

Data table
ID_REF VALUE
A_24_P66027 257.7165617
A_32_P77178 62.48207223
A_23_P212522 152.5434586
A_24_P934473 68.10224149
A_24_P9671 7870.866544
A_32_P29551 37.51505414
A_24_P801451 298.4834144
A_32_P30710 10478.11946
A_32_P89523 85.60138486
A_24_P704878 35.74111748
A_32_P86028 12342.16152
A_24_P470079 36.32342502
A_23_P65830 1644.596618
A_24_P595567 39.90653479
A_24_P391591 124.7026936
A_24_P799245 31.09818041
A_24_P932757 51.02020635
A_24_P835500 539.769197
A_23_P54340 37.15844566
A_23_P67555 80.41546744

Total number of rows: 40704

Table truncated, full table size 976 Kbytes.




Supplementary file Size Download File type/resource
GSM1092253_jhu_251485070373_S01_GE2_107_Sep09_1_2_MCF7_Mock_Day3_RNA-Cy3_MCF7_AZA_Day3_RNA_Cy5.txt.gz 15.3 Mb (ftp)(http) TXT
Processed data included within Sample table

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