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Sample GSM865734 Query DataSets for GSM865734
Status Public on Mar 25, 2012
Title HEK293
Sample type RNA
 
Source name HEK293 human embryonic kidney
Organism Homo sapiens
Characteristics cell line: HEK293
cell type: embryonic kidney
origin: non-lymphoid
Treatment protocol Not treated.
Growth protocol B-LCLs and B cells were grown in RPMI 1640 medium supplemented with 25mM HEPES, 2mM L-glutamine, 10% heat-inactivated fetal bovine serum and penicillin-streptomycin. HEK293 and HeLa cells were grown in DMEM medium supplemented with 2mM L-glutamine, 10% heat-inactivated fetal bovine serum and penicillin-streptomycin. Exponential growth under normal conditions.
Extracted molecule total RNA
Extraction protocol Total RNA was isolated with the miRNeasy mini kit, including on-column DNase I treatment (Qiagen), according to the manufacturer’s instructions. Total RNA was quantified using the NanoDrop 2000 (Thermo Scientific) and RNA quality was assessed with the 2100 Bioanalyzer (Agilent Technologies).
Label Cy3
Label protocol 100 ng of each RNA sample was labeled with the microRNA complete labeling and hybridization kit (Agilent Technologies) according to the manufacturer’s instructions.
 
Hybridization protocol Labeled RNA was hybridized to the Agilent Human microRNA Microarray Release 16.0 (G4872A-031181 Agilent Technologies) with the microRNA complete labeling and hybridization kit (Agilent Technologies) according to the manufacturer’s instructions.
Scan protocol Slides were scanned with a GenePix 4000B scanner (Molecular Devices) at a 5uM/pixel resolution .
Data processing Features were extracted with the GenePix 6.1 software. Analyses were performed using BRB-ArrayTools Version 4.2.0 Stable Release developed by Dr. Richard Simon and the BRB-ArrayTools Development Team (http://en.bio-soft.net/chip/BRBArrayTools.html). The data were background-subtracted and quantile normalized. To estimate a single intensity measure for each miRNA, we calculated the mean of its different probes.
 
Submission date Jan 24, 2012
Last update date Mar 25, 2012
Contact name Diana Paola Granados
Organization name IRIC
Department Medecine
Lab Immunobiologie
Street address C.P. 6128, succursale Centre-ville
City Montreal
State/province Quebec
ZIP/Postal code H3C 3J7
Country Canada
 
Platform ID GPL15159
Series (1)
GSE35319 MHC I-associated peptides preferentially derive from transcripts bearing miRNA response elements

Data table header descriptions
ID_REF
VALUE Log2 normalized signal intensity

Data table
ID_REF VALUE
A_25_P00010019 9.899106026
A_25_P00010020 9.746421814
A_25_P00010021 9.694145203
A_25_P00010023 10.01672077
A_25_P00010041 9.972067833
A_25_P00010042 9.622063637
A_25_P00010043 null
A_25_P00010044 9.530994415
A_25_P00010047 9.764862061
A_25_P00010048 9.971268654
A_25_P00010053 10.03620052
A_25_P00010054 9.831382751
A_25_P00010062 9.663237572
A_25_P00010063 10.22989941
A_25_P00010070 11.52218342
A_25_P00010071 11.44674397
A_25_P00010072 11.03273964
A_25_P00010073 10.471838
A_25_P00010078 9.394049644
A_25_P00010079 9.825312614

Total number of rows: 3523

Table truncated, full table size 90 Kbytes.




Supplementary file Size Download File type/resource
GSM865734.txt.gz 2.0 Mb (ftp)(http) TXT
Processed data included within Sample table

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