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Sample GSM1686185 Query DataSets for GSM1686185
Status Public on Dec 31, 2015
Title Primary prostate p53-/- Rbf/f 1
Sample type RNA
Source name Prostate, lacZ
Organism Mus musculus
Characteristics tissue: prostate
genotype: p53-/- Rbf/f
rb status: Intact
pten status: Intact
Treatment protocol Prostate cells were infected with adeno virus (lacZ) as a control or adeno virus (Cre) for deleting Rb overnight followed by changing of media. RNA was extracted after infection by 48 hours.
Growth protocol Prostate cells were cultured in FBS lack Prostacult media supplemented with bFGF and bEGF
Extracted molecule total RNA
Extraction protocol Total RNA was extracted using RNeasy Mini Kit (#74106, Qiagen) according to the manufacturer’s instruction. RNA was quantified, and quality was monitored by the Agilent 2100 Bioanalyzer (Agilent Technologies, Santa Clara, CA).
Label Cy3
Label protocol Cyanine-3 (Cy3) labeled cRNA was prepared from 200 ng of total RNA using the One-Color Low Input Quick Amp Labeling kit (Agilent) according to the manufacturer's instructions with some changes. 3rd Spike mix was made by diluted 2nd Spike-Mix 10 times, and 1.8 ul of 3rd Spike-Mix was added to samples. Cy3 labeled cRNA was synthesized at 40°C for 2 hours and purified by RNAeasy column purification (QIAGEN, Valencia, CA). Dye incorporation and cRNA yield were checked with the NanoDrop ND-1000 Spectrophotometer.
Hybridization protocol 1.65 ug of Cy3-labelled cRNA (specific activity >6.0 pmol Cy3/ug cRNA) was fragmented at 60°C for 30 minutes in a reaction volume of 55 ul containing 1x Agilent fragmentation buffer and 2x Agilent blocking agent following the manufacturers instructions. On completion of the fragmentation reaction, 55 ul of 2x Agilent hybridization buffer was added to the fragmentation mixture and hybridized to Agilent Mouse Whole Genome Microarray 4x44K v2 for 17 hours at 65°C in a rotating Agilent hybridization oven. After hybridization, microarrays were washed 1 minute at room temperature with GE Wash Buffer 1 (Agilent) and 1 minute with 37°C GE Wash buffer 2 (Agilent), then dried by raise it slowly from buffer 2.
Scan protocol Slides were scanned immediately after washing on the Agilent DNA Microarray Scanner (G2505B) using one color scan setting for 4x44k array slides (Scan Area 61x21.6 mm, Scan resolution 5um, Dye channel is set to Green.
Description Gene expression of control p53-/- prostate cells in the presence of Rb
Data processing The scanned images were analyzed with Feature Extraction Software (Agilent) using default parameters (protocol GE1_107_Sep09 and Grid: 026655_D_F_20120201) to obtain background subtracted and spatially detrended Processed Signal intensities. Features flagged in Feature Extraction as Feature Non-uniform outliers were excluded. Entities having Detected flag across all samples were extracted.
Submission date May 14, 2015
Last update date Dec 31, 2015
Contact name Takumi Nishiuchi
Organization name Kanazawa University
Street address 13-1 Takaramachi
City Kanazawa
ZIP/Postal code 920-0934
Country Japan
Platform ID GPL11202
Series (2)
GSE68903 Development of gene sets after deleting Rb in p53 null background primary prostate cells [Rb only]
GSE68905 Development of gene sets after deleting Rb or Rb and Pten in p53 null background primary prostate cells

Data table header descriptions
VALUE Normalized Signal intensity

Data table
GE_BrightCorner 3.684699
A_55_P2022211 1.6316051
A_55_P1964375 1.7755032
A_51_P128876 5.466978
A_51_P207591 -2.6188269
A_55_P2131920 3.0362062
A_55_P2404223 -2.1850367
A_55_P2101944 1.5468874
A_52_P358860 0.5037041
A_51_P119031 -0.78827477
A_51_P343900 3.0375834
A_51_P487813 3.4328737
A_52_P613977 1.5277977
A_52_P549166 0.2693491
A_55_P2052210 4.5630627
A_51_P128987 4.534109
A_55_P1958431 -4.6938477
A_55_P2111153 1.1544685
A_51_P210560 1.9666061
A_55_P2048493 -2.9441996

Total number of rows: 22177

Table truncated, full table size 520 Kbytes.

Supplementary file Size Download File type/resource
GSM1686185_SG12060621_252665516620_S01_GE1_1100_Jul11_1_1.txt.gz 2.2 Mb (ftp)(http) TXT
Processed data included within Sample table

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