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Sample GSM375305 Query DataSets for GSM375305
Status Public on Feb 11, 2010
Title Adjacent normal tissue from patient 221334-1
Sample type RNA
 
Source name human
Organism Homo sapiens
Characteristics tissue: Adjacent normal tissue from patient 221334-1
Extracted molecule total RNA
Extraction protocol Total RNA was extracted with TRIZOL reagent (Invitrogen, Carlsbad, CA) and the low-molecular-weight RNA was isolated by using the Ambion miRNA Isolation Kit
Label Cy3
Label protocol 4 ug of low-molecular-weight RNA was labeled with 500 ng of 5'-phosphate-cytidyl-uridyl-cy3-3' (Dharmacon, Lafayette, CO) with 2 units T4 RNA ligase (New England Biolabs, Ipswich, MA). The labeling reaction was performed at 4oC for 2 h. Labeled RNA was precipitated with 0.3 M sodium acetate and 2.5 volumes ethanol and after washing with ethanol and drying was resuspended in 15 ¦Ìl of hybridization buffer containing 3¡ÁSSC, 0.2% SDS and 15% formamide.
 
Hybridization protocol Hybridization was performed at 42oC under LifterSlipTM (Erie, Portsmouth, NH) in a hybridization chamber which was placed in a 3D-tilting agitator BioMixerTM II (CapitalBio) to provide continuous mixing of the hybridization buffer that results in more uniform hybridization across the entire slide surface, preventing edge effects and giving improved signal intensity, the efficiency of which has been demonstrated with our genome-wide mRNA expression profiling (Patterson et al., Nat Biotechnol. 2006, 24:1140-1150).The array was then washed with two consecutive washing solutions of 0.2% SDS, 2¡ÁSSC at 42¡ãC for 5 min, and 0.2% SSC for 5 min at room temperature
Scan protocol Arrays were scanned with a LuxScanTM 10K-A laser confocal scanner and the images obtained were then analyzed using LuxScan 3.0TM software (both from CapitalBio, Beijing, China)
Description the microRNA expression in the tissue
Data processing After average values of the replicate spots of each miRNA were background subtracted, faint spots were filtered out when expression signal were lower than 800 in all samples.
 
Submission date Feb 25, 2009
Last update date Mar 03, 2009
Contact name wu jp
E-mail(s) [email protected]
Fax (86)-10-62773059
Organization name National Engineering Research Center
Street address 18 Life Science Parkway
City beijing
ZIP/Postal code 102206
Country China
 
Platform ID GPL8176
Series (1)
GSE15008 MicroRNA Expression Profile Reveals Important Clinical Tools for the Pathology of Lung Cancer

Data table header descriptions
ID_REF
VALUE the signal intensity after calibration

Data table
ID_REF VALUE
1 11507
2 11107
3 14887
4 2172
5 2260
6 2555
7 7692
8 8388
9 9484
10 48314
11 49637
12 55995
13 36908
14 36406
15 40757
16 10804
17 11622
18 12087
19 769
20 955

Total number of rows: 3696

Table truncated, full table size 32 Kbytes.




Supplementary file Size Download File type/resource
GSM375305.txt.gz 24.4 Kb (ftp)(http) TXT
Processed data included within Sample table

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