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Sample GSM1811622 Query DataSets for GSM1811622
Status Public on Dec 21, 2015
Title SG-3
Sample type RNA
 
Source name Salivary gland
Organism Homo sapiens
Characteristics tissue: salivary gland
Extracted molecule total RNA
Extraction protocol After fresh tissues were homogenized by TissueLyser, total RNA was extracted by ISOGEN.
Label digoxigenin
Label protocol Digoxigenin-UTP-labelled cRNA was generated and amplified from 1 mg of total RNA using Applied Biosystems Chemiluminescent RT-IVT Labelling Kit.
 
Hybridization protocol Ten mg of labelled cRNA was hybridized to each pre-hybridized microarray at 55℃ for 16 hours.
Scan protocol After Chemiluminescence detection using Applied Biosystems Chemiluminescence Detection Kit, images were collected by the AB1700 Chemiluminescent Microarray Analyzer.
Data processing The quantile method was used for background correction and normalization.
 
Submission date Jul 07, 2015
Last update date Dec 21, 2015
Contact name Koh-ichi Nakashiro
E-mail(s) [email protected]
Phone +81899605393
Organization name Ehime University Graduate School of Medicine
Department Oral and Maxillofacial Surgery
Street address 454 Shitsukawa
City Toon
State/province Ehime
ZIP/Postal code 791-0295
Country Japan
 
Platform ID GPL2986
Series (1)
GSE70604 Gene expression profiles in lymph nodes with metastasis of oral squamous cell carcinoma (OSCC)

Data table header descriptions
ID_REF
VALUE GeneSpring GX 13.0-software computed normalized signal intensity (log2)

Data table
ID_REF VALUE
100002 13.387316
100003 7.785521
100027 9.824656
100036 8.326749
100037 8.313447
100039 10.244279
100044 7.6606936
100045 9.34727
100051 8.907421
100052 6.9543085
100057 10.113823
100058 13.690095
100060 11.442526
100062 7.7666707
100064 8.5311365
100079 12.336558
100089 14.13104
100093 8.001366
100095 8.544862
100100 11.530792

Total number of rows: 32878

Table truncated, full table size 528 Kbytes.




Supplementary data files not provided
Processed data included within Sample table

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