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Sample GSM2428922 Query DataSets for GSM2428922
Status Public on Dec 14, 2016
Title iPSC-CM_donorH_rep3
Sample type RNA
 
Source name iPSC-CM_donorH
Organism Homo sapiens
Characteristics cell type: iPSC-CM
donor: H
Extracted molecule total RNA
Extraction protocol Total RNA was purified with an RNeasy Mini Kit (Qiagen) following the manufacturer's protocol.
Label Cy3
Label protocol Cyanine-3 (Cy3) labeled cRNA was prepared from 0.1 ug RNA using the One-Color Low RNA Input Quick Amplification Labeling kit (Agilent) according to the manufacturer's instructions, followed by RNAeasy column purification (QIAGEN). Dye incorporation and cRNA yield were checked with the NanoDrop ND-1000 Spectrophotometer.
 
Hybridization protocol 0.6 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 250 ml containing 1x Agilent fragmentation buffer and 2x Agilent blocking agent following the manufacturers instructions. On completion of the fragmentation reaction, 250 ml of 2x Agilent hybridization buffer was added to the fragmentation mixture and hybridized to Agilent SurePrint G3 Human GE v2 8x60K Microarray (G039494) 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 immediately by brief centrifugation.
Scan protocol Slides were scanned immediately after washing on the Agilent DNA Microarray Scanner (G2505B) using one color scan setting for 8x60k array slides (Scan Area 61x21.6 mm, Scan resolution 10um, Dye channel is set to Green and Green PMT is set to 100%).
Description 5-1CM-3
Data processing The scanned images were analyzed with Feature Extraction Software 10.7.1.1 (Agilent) using default parameters (protocol GE1_107_Sep09 and Grid: 039494_D_F_20140813) to obtain background subtracted and spatially detrended Processed Signal intensities. Features flagged in Feature Extraction as Feature Non-uniform outliers were excluded.
 
Submission date Dec 14, 2016
Last update date Dec 14, 2016
Contact name Tadahiro Shinozawa
E-mail(s) [email protected]
Organization name Takeda pharmaceuticals
Street address Muraokahigashi 2chome
City Fujisawa
ZIP/Postal code 251-8555
Country Japan
 
Platform ID GPL17077
Series (1)
GSE92391 Global gene expression of hiPS cell derived cardiomyocytes from healthy volunteers

Data table header descriptions
ID_REF
VALUE Normalized signal intensity

Data table
ID_REF VALUE
(+)E1A_r60_1 0.012024486
(+)E1A_r60_3 0.079682968
(+)E1A_r60_a104 0.106236417
(+)E1A_r60_a107 0.134907373
(+)E1A_r60_a135 0.112477785
(+)E1A_r60_a20 0.210339251
(+)E1A_r60_a22 1.698612298
(+)E1A_r60_a97 0.048549593
(+)E1A_r60_n11 0.092977362
(+)E1A_r60_n9 0.045912242
3xSLv1 0.005660323
A_19_P00315452 0.062392983
A_19_P00315459 0.085326247
A_19_P00315482 0.130179628
A_19_P00315492 0.505276945
A_19_P00315493 0.045393137
A_19_P00315502 0.047944795
A_19_P00315506 1.670824878
A_19_P00315518 0.045230617
A_19_P00315519 0.023163537

Total number of rows: 50739

Table truncated, full table size 1259 Kbytes.




Supplementary file Size Download File type/resource
GSM2428922_US09503747_253949440290_S01_GE1_107_Sep09_2_3.txt.gz 3.1 Mb (ftp)(http) TXT
Processed data included within Sample table

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