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Sample GSM1515576 Query DataSets for GSM1515576
Status Public on Mar 31, 2016
Title HeLa haboring control shRNA #1
Sample type RNA
 
Source name HeLa, control, rep1
Organism Homo sapiens
Characteristics cell type: HeLa
transfectant: control shRNA
Treatment protocol AK4 was knockdown by shRNA
Growth protocol DMEM with 10% FBS
Extracted molecule total RNA
Extraction protocol Total RNA was isolated from cells using TRIzol Reagent (nitrogen) and purified using SV Total RNA Isolation System (Promega)
Label Cy3
Label protocol cRNA was amplified and labelled using a Low input Quick Amp Labelling Kit (Agilent Technologies).
 
Hybridization protocol cRNA was hybridized to a 44K 60-mer oligomicroarray SurePrint G3 Human GE Microarray Kit 8x60K v2 ; Agilent Technologies) according to the manufacturer's instructions.
Scan protocol The hybridized microarray slides were scanned using an Agilent scanner. The relative hybridization intensities and background hybridization values were calculated using Feature Extraction Software version 9.5.1.1 (Agilent Technologies).
Data processing The scanned images were analyzed with Feature Extraction Software 9.5.1.1 (Agilent) using default parameters to obtain background subtracted and spatially detrended Processed Signal intensities. The raw signal intensities and flags for each probe were calculated from the hybridization intensities and spot information according to the procedures recommended by Agilent Technologies using the Flag criteria in the GeneSpring Software. In addition, the raw signal intensities of seven samples were normalized by the quantile algorithm with the Bioconductor.
 
Submission date Sep 29, 2014
Last update date Mar 31, 2016
Contact name Koichi Fujisawa
E-mail(s) fujisawa@yamaguchi-u.ac.jp
Organization name Yamaguchi University Graduate School of Medicine
Department Department of Gastroenterology and Hepatology
Street address 1-1-1, minami-kogushi
City Ube
State/province Yamaguchi
ZIP/Postal code 755-8505
Country Japan
 
Platform ID GPL17077
Series (1)
GSE61843 Inhibition of AK4 expression increases drug sensitivity and elevates mitochondrial ATP synthesis

Data table header descriptions
ID_REF
VALUE quantile normalized signal, non-log scaled
ABS_CALL

Data table
ID_REF VALUE ABS_CALL
A_19_P00315452 72.48959571 P
A_19_P00315459 445.0084143 P
A_19_P00315482 21.32455286 P
A_19_P00315492 16.31466286 A
A_19_P00315493 66.07302571 P
A_19_P00315502 3098.694714 P
A_19_P00315506 504.3329571 P
A_19_P00315518 5.693949571 A
A_19_P00315519 3.815936571 A
A_19_P00315524 19.97310286 P
A_19_P00315528 6.570597429 A
A_19_P00315529 5.205685429 A
A_19_P00315538 3.640239429 A
A_19_P00315541 13.35711143 A
A_19_P00315543 85.31533286 P
A_19_P00315550 271.3074429 P
A_19_P00315551 228.6426 P
A_19_P00315554 8.602743857 A
A_19_P00315581 4869.888025 P
A_19_P00315583 104.1213149 P

Total number of rows: 50599

Table truncated, full table size 1340 Kbytes.




Supplementary file Size Download File type/resource
GSM1515576_US11030397_253949422683_S01_GE1_107_Sep09_1_1.txt.gz 12.4 Mb (ftp)(http) TXT
Processed data included within Sample table

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