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Sample GSM914021 Query DataSets for GSM914021
Status Public on Jul 26, 2013
Title Basal cells_Patient6
Sample type RNA
 
Source name Basal cells
Organism Homo sapiens
Characteristics gender: Female
age: 29
cell type: Lin-CD49fhiEpCAMneg/low (basal stem/bipotent cell-enriched)
Extracted molecule total RNA
Extraction protocol Human breast tissues obtained from reduction mammoplasty surgeries were collected, processed and single cells FACS purified as described by Eirew et al Nature Medicine (PMID 19029987).
RNA was isolated from approximately a million cells in Trizol (Invitrogen), re-purified using the RNeasy Micro kit (Qiagen), and total RNA quality was assessed with the Agilent 2100 bioanalyzer prior to microarray analysis. Samples with a RIN value of greater than or equal to 8.0 were deemed to be acceptable for microarray analysis.
Label Cy3
Label protocol Cyanine-3 (Cy3) labeled cRNA was prepared from about 25ng RNA using Agilent One-Color Microarray-Based Exon Analysis Low Input Quick Amp WT Labeling v1.0 according to the manufacturer's instructions, followed by RNAeasy column purification (QIAGEN, Valencia, CA). Dye incorporation and cRNA yield were checked with the NanoDrop ND-1000 Spectrophotometer.
 
Hybridization protocol 600ng of Cy3-labelled cRNA (specific activity >15 pmol Cy3/ug cRNA) was fragmented at 60°C for 30 minutes in a reaction volume of 25ul containing 1ul Agilent fragmentation buffer and 5ul of 10X Agilent blocking agent following the manufacturers instructions. On completion of the fragmentation reaction, 25ul of 2x Agilent hybridization buffer was added to the fragmentation mixture and hybridized to Agilent SurePrint G3 Human 8x60K Microarrays (Design ID 028004) 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 for 1min in acetonitrile.
Scan protocol Arrays were scanned with the Agilent DNA Microarray Scanner at a 3um scan resolution.
Description Patient-6, Lin-CD49fhiEpCAMneg/low (basal stem/bipotent cell-enriched)
Data processing Data was processed with Agilent Feature Extraction 10.10.
 
Submission date Apr 12, 2012
Last update date Jul 26, 2013
Contact name Connie Eaves
E-mail(s) ceaves@bccrc.ca
Phone (+1) 604-675-8109
Fax (+1) 604-877-0712
URL http://www.terryfoxlab.ca/people/ceaves/connie.aspx
Organization name BC Cancer Agency
Department Terry Fox Laboratory
Lab Eaves Lab
Street address 675 W 10th Ave
City Vancouver
State/province BC
ZIP/Postal code V5Z 1L3
Country Canada
 
Platform ID GPL14550
Series (1)
GSE37223 Global gene expresion profile of phenotypically distinct human mammary epithelial subpopulations of various developmental age

Data table header descriptions
ID_REF
VALUE Quantile normalized (using Agilent GeneSpring 11.5.1) signal intensity

Data table
ID_REF VALUE
A_23_P326296 5.5901394
A_24_P287941 3.9408588
A_24_P325046 2.3247077
A_23_P200404 11.283821
A_19_P00800513 11.027411
A_23_P15619 2.0299408
A_33_P3402354 4.694824
A_33_P3338798 2.0270216
A_32_P98683 8.978131
A_23_P137543 6.980032
A_19_P00803040 10.553831
A_23_P117852 3.4106042
A_33_P3285585 2.0173388
A_24_P328231 5.83942
A_33_P3415668 2.0107236
A_23_P73609 2.4361527
A_24_P186124 7.6371727
A_23_P369983 6.8685327
ERCC-00071_128 2.5041711
ERCC-00142_99 2.1476352

Total number of rows: 42543

Table truncated, full table size 962 Kbytes.




Supplementary file Size Download File type/resource
GSM914021_252800415172_03062012_S01_GE1_1010_Sep10_1_3.txt.gz 3.1 Mb (ftp)(http) TXT
Processed data included within Sample table

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