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Sample GSM1102831 Query DataSets for GSM1102831
Status Public on Mar 21, 2013
Title Primary ESCC tissue from patient 3 with ESCC
Sample type RNA
Source name surgical speciment from normal esophageal tissue
Organism Homo sapiens
Characteristics tissue: primary esophageal sqaumous cell cancer (ESCC)
gender: Male
age: 70
Treatment protocol Primary tumours and adjacent non-neoplastic tissues were obtained from patients with esophageal squamous cell cancer who underwent surgical treatment, the samples were immeidately stored in liquid nitroge tank.
Growth protocol N/A
Extracted molecule total RNA
Extraction protocol Total RNAs were extracted using Trizol reagent (Invitrogen, Carlsbad, CA, USA) following manufacturer’s instruction. RNA was quantified using a NanoDrop-1000 spectrophotometer and quality was monitored with the Agilent 2100 Bioanalyzer (Agilent Technologies, Santa Clara, CA).
Label Cy3
Label protocol Cyanine-3 (Cy3) labeled cRNA was prepared from 100ng of total RNA using One-Color Microarray-Based Gene Expression Analysis Low Input Quick Amp Labeling v6.0 (Agilent) following manufacture's instruction, followed by RNAeasy column purification (QIAGEN, Valencia, CA). Dye incorporation and cRNA yield were checked with the NanoDrop ND-1000 Spectrophotometer.
Hybridization protocol 1600ng 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 50 ul containing 1x Agilent fragmentation buffer and 2x Agilent blocking agent following the manufacturers instructions. On completion of the fragmentation reaction, 50 ul of 2x Agilent hybridization buffer was added to the fragmentation mixture and hybridized to Agilent SurePrint G3 Human GE 8x60K Microarray (Design ID 028004) 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 with acetonitrile for 1 min.
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 3um, 20 bit tiff file, Dye channel is set to Green and Green PMT is set to 100%).
Description primary ESCC tissue
Data processing The scanned images were analyzed with Feature Extraction Software (Agilent) using default parameters (protocol GE1_1100_Jul11and Grid:028004_D_F_20120411) to obtain background subtracted and spatially detrended Processed Signal intensities. Features flagged in Feature Extraction as Feature Non-uniform outliers were excluded.
Submission date Mar 20, 2013
Last update date Mar 21, 2013
Contact name Wei Wu
Organization name 1.Zhengzhou Central Hospital, Affiliated to Zhengzhou University, China; 2. University of Calgary
Street address 3330 Hospital Dr. NW
City Calgary
ZIP/Postal code T2N 4N1
Country Canada
Platform ID GPL13607
Series (1)
GSE45350 Genome-wide screening of the expression of long noncoding RNA and coding RNA expression in esophageal sqaumous cell cancer

Data table header descriptions
VALUE normalized signal intensity

Data table
1 95091.68
2 6.08454
3 6.083683
4 447.0662
5 536.7828
6 84.97233
7 4740.851
8 6048.716
9 49.77187
10 116.1047
11 122.4237
12 1749.661
13 1930.052
14 1668.804
15 6988.994
16 6.016818
17 43.71875
18 5.999466
19 59.94513
20 701.6575

Total number of rows: 62976

Table truncated, full table size 904 Kbytes.

Supplementary file Size Download File type/resource
GSM1102831_ESCC_3T.txt.gz 3.1 Mb (ftp)(http) TXT
Processed data included within Sample table
Processed data provided as supplementary file

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