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Sample GSM1092260 Query DataSets for GSM1092260
Status Public on Jul 12, 2013
Title MDA-MB-468_day3_expression
Sample type RNA
 
Source name MDA-MB-468 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 MDA-MB-468_day3
jhu_251485067910_S01_GE2_107_Sep09_1_2_MDA453 Mock Day3-Cy3_MDA453 AZA Day3-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 1103.821672
A_32_P77178 66.31053516
A_23_P212522 238.5702963
A_24_P934473 81.21783534
A_24_P9671 4035.457347
A_32_P29551 43.85339238
A_24_P801451 761.8722081
A_32_P30710 9808.467393
A_32_P89523 70.75847249
A_24_P704878 40.25690485
A_32_P86028 9747.131542
A_24_P470079 65.97870411
A_23_P65830 666.20191
A_24_P595567 68.76200527
A_24_P391591 189.9762962
A_24_P799245 37.7908473
A_24_P932757 42.06102596
A_24_P835500 967.5845699
A_23_P54340 47.66248321
A_23_P67555 110.8696453

Total number of rows: 40704

Table truncated, full table size 975 Kbytes.




Supplementary file Size Download File type/resource
GSM1092260_jhu_251485067910_S01_GE2_107_Sep09_1_2_MDA453_Mock_Day3-Cy3_MDA453_AZA_Day3-Cy5.txt.gz 15.4 Mb (ftp)(http) TXT
Processed data included within Sample table

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