NCBI Logo
GEO Logo
   NCBI > GEO > Accession DisplayHelp Not logged in | LoginHelp
GEO help: Mouse over screen elements for information.
          Go
Sample GSM1092266 Query DataSets for GSM1092266
Status Public on Jul 12, 2013
Title ZR-75-30_day3_expression
Sample type RNA
 
Source name ZR-75-30 breast cancer cell line, day 3
Organism Homo sapiens
Characteristics gender: Female
disease: Breast cancer
er: +
her2: +
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 ZR-75-30_day3
jhu_251485070425_S01_GE2_107_Sep09_1_2_ZR-75-30 Mock Day3 RNA-Cy3_ZR-75-30 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 351.1182497
A_32_P77178 83.64121321
A_23_P212522 177.1595642
A_24_P934473 80.46092463
A_24_P9671 5661.684281
A_32_P29551 39.01187742
A_24_P801451 338.9302101
A_32_P30710 32612.38413
A_32_P89523 72.58577199
A_24_P704878 44.54836638
A_32_P86028 15002.70514
A_24_P470079 50.39753076
A_23_P65830 1174.678986
A_24_P595567 61.97666188
A_24_P391591 101.2939597
A_24_P799245 36.88403969
A_24_P932757 47.04251501
A_24_P835500 4672.604563
A_23_P54340 45.30257447
A_23_P67555 84.20996716

Total number of rows: 40704

Table truncated, full table size 976 Kbytes.




Supplementary file Size Download File type/resource
GSM1092266_jhu_251485070425_S01_GE2_107_Sep09_1_2_ZR-75-30_Mock_Day3_RNA-Cy3_ZR-75-30_AZA_Day3_RNA_Cy5.txt.gz 15.3 Mb (ftp)(http) TXT
Processed data included within Sample table

| NLM | NIH | GEO Help | Disclaimer | Accessibility |
NCBI Home NCBI Search NCBI SiteMap