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Sample GSM1050566 Query DataSets for GSM1050566
Status Public on Jul 17, 2013
Title Pten-/-;Dicer wild-type, sample 4
Sample type RNA
 
Channel 1
Source name Dicer wild-type
Organism Mus musculus
Characteristics strain background: C57BL/6
genotype/variation: Pten-/-; Dicer wild-type
tissue: Cancerous urogenital tissues
Growth protocol The ARR2PB-Cre transgenic mice were from Dr. Fen Wang at the Institute of Bioscience and Technology, Texas A&M Health Science Center. The Ptenfl/fl mice were from Dr. Hong Wu at the University of California Los Angeles. ARR2PB-Cre;Ptenfl/fl;Dicerfl/wt female mice and Ptenfl/fl;Dicerfl/wt male mice were mated to generated ARR2PB-Cre;Ptenfl/fl, ARR2PB-Cre;Ptenfl/fl;Dicerfl/wt, and ARR2PB-Cre;Ptenfl/fl;Dicerfl/fl mice.
Extracted molecule total RNA
Extraction protocol Trizol extraction of total RNA was performed according to the manufacturer's instructions. Microarray analysis was performed using 2.5 micrograms of total RNA.
Label Alexa Fluor 647
Label protocol Complementary DNA (cDNA) reverse transcription and fluorescent labeling reactions were carried out using SuperScript Plus Direct cDNA Labeling system (Invitrogen, Carlsbad, CA).
 
Channel 2
Source name mouse, universal reference RNA
Organism Mus musculus
Characteristics sample type: Stratagene, Universal Mouse Reference RNA Catalog #740100
Growth protocol The ARR2PB-Cre transgenic mice were from Dr. Fen Wang at the Institute of Bioscience and Technology, Texas A&M Health Science Center. The Ptenfl/fl mice were from Dr. Hong Wu at the University of California Los Angeles. ARR2PB-Cre;Ptenfl/fl;Dicerfl/wt female mice and Ptenfl/fl;Dicerfl/wt male mice were mated to generated ARR2PB-Cre;Ptenfl/fl, ARR2PB-Cre;Ptenfl/fl;Dicerfl/wt, and ARR2PB-Cre;Ptenfl/fl;Dicerfl/fl mice.
Extracted molecule total RNA
Extraction protocol Trizol extraction of total RNA was performed according to the manufacturer's instructions. Microarray analysis was performed using 2.5 micrograms of total RNA.
Label Alexa Fluor 555
Label protocol Complementary DNA (cDNA) reverse transcription and fluorescent labeling reactions were carried out using SuperScript Plus Direct cDNA Labeling system (Invitrogen, Carlsbad, CA).
 
 
Hybridization protocol The sample and reference probes were mixed with GEx hybridization buffer and blocking solution (Agilent, Santa Clara, CA) and denatured by a 2-minute incubation at 95 degC. Probes were hybridized to Agilent 4x44K Whole Mouse Genome arrays and rotating over night at 65 degC.
Scan protocol Slide were scanned in an Agilent Microarray Scanner and the data were analyzed using Agilent Feature Extraction Software (v.9.1).
Description 36086_166_WT_4
Data processing LOWESS normalized, background subtracted data obtained from log2 of processed Red signal/processed Green signal. Agilent and Bioconductor software (v.2.11) was used.
 
Submission date Dec 10, 2012
Last update date Jul 17, 2013
Contact name Chad Creighton
E-mail(s) [email protected]
Organization name Baylor College of Medicine
Department Biostatistics, Ducan Cancer Center
Street address One Baylor Plaza, Mail Stop: BCM305
City Houston
State/province TX
ZIP/Postal code 77030
Country USA
 
Platform ID GPL4134
Series (1)
GSE42820 Gene expression changes resulting from attenuation of Dicer activity

Data table header descriptions
ID_REF
VALUE log2 ratio of transcript abundance of the sample versus a universal RNA reference

Data table
ID_REF VALUE
1 0.558411983
2 -0.026332294
3 0.095834454
4 0.058974947
5 0.089120735
6 0.300727598
7 0.053523776
8 0.079878878
9 0.089076402
10 0.159708926
11 0.381334095
12 0.520309558
13 0.043821216
14 0.175220019
15 0.100016996
16 0.300751382
18 -0.190168236
19 -0.290123501
20 -0.224182485
21 0.04609116

Total number of rows: 45018

Table truncated, full table size 797 Kbytes.




Supplementary file Size Download File type/resource
GSM1050566_36086_166_WT_4.txt.gz 4.3 Mb (ftp)(http) TXT
Processed data included within Sample table

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