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Sample GSM3754790 Query DataSets for GSM3754790
Status Public on Mar 15, 2020
Title B1364-1: Gastritis
Sample type RNA
Source name Gastritis
Organism Homo sapiens
Characteristics tissue: gastric
gender: Female
age: 58
Treatment protocol Biopsy forceps were used to clamp the tissue from the suspected gastric mucosa and adjacent normal gastric mucosa that were at least 5 cm from the lesion location. Gastroscopic biopsy tissues were rapidly immersed in RNA later after being isolated and transferred to a -80° C refrigerator for long-term storage after overnight storage at 4° C.
Extracted molecule total RNA
Extraction protocol Total RNA was extracted from frozen tissues using the RNeasy Mini Kit (Cat No. 74106, Qiagen, Germany) according to the manufacturer’s instructions. RNA concentrations were determined using a NanoDrop ND-2000 Spectrophotometer (NanoDrop Technologies, Wilmington, USA), and RNA integrity was evaluated using a 2100 Bioanalyzer (Agilent Technologies, Santa Clara, CA, USA).
Label Cy3
Label protocol CTP-cyanine-3 (Cy3) labeled cRNA was prepared from 100 ng RNA using the One-Color Microarray-Based Gene Expression Analysis (Agilent, version 6.6) according to manufacturer's instructions, followed by RNeasy column purification (RNeasy Mini kit, QIAGEN). Dye incorporation and cRNA yield and quality were checked by spectrophotometry (Nanodrop ND1000, Labtech) and with the Agilent 2100 Bioanalyser.
Hybridization protocol 600 ng of CTP-Cy3-labelled cRNA (specific activity > 10.0 pmol Cy3/µg cRNA) was fragmented at 60°C for 30 min in a reaction volume of 25 µl containing 25 x Agilent fragmentation buffer and 10 x Agilent blocking agent following the manufacturers instructions. On completion of the fragmentation reaction, 25 µl of 2 x Agilent hybridization buffer were added to the fragmentation mixture and hybridized to SurePrint G3 Human GE v2 8x60K (Agilent) for 17 h at 65°C in a rotating hybridization oven. After hybridization, microarrays were washed 1 min at room temperature with GE Wash Buffer 1 (Agilent) and 1 min with 37°C GE Wash buffer 2 (Agilent), then dried immediately by brief passage in acetonitrile.
Scan protocol Slides were scanned immediately after washing on the Agilent DNA Microarray Scanner (G2565CA) using one color scan setting for 8x60k array slides: scan area was 61x21.6 mm, scan resolution 3 µm, dye channel was set to Green, Tiff file dynamic range was 20 bits and Green PMT was set to 100 %.
Description paired control sample of B1364-2
Data processing The raw data were normalized using GeneSpring GX software, version 11.5 (Silicon Genetics, Redwood City, CA, USA). The expression value for a particular gene was determined as the median value of all probes mapping to this gene.
Submission date May 07, 2019
Last update date Mar 16, 2020
Contact name Yajing Zhang
Phone 8618800193022
Organization name Peking Union Medical College
Street address no.17 Panjiayuan Nanli
City Beijing
State/province Beijing
ZIP/Postal code 100021
Country China
Platform ID GPL17077
Series (1)
GSE130823 Dissecting Expression Profiles of Gastric Precancerous Lesions and Early Gastric Cancer to Explore Crucial Molecules in Intestinal-type Gastric Cancer Tumorigenesis

Data table header descriptions
VALUE Normalized signal intensity

Data table
GE_BrightCorner 0.106479645
DarkCorner 0.21954131
A_23_P117082 -0.1314125
A_33_P3246448 1.1851931
A_33_P3318220 0.01607263
A_33_P3236322 -0.89931715
A_33_P3319925 -1.0066304
A_21_P0000509 -0.90184975
A_21_P0000744 0.60019255
A_24_P215804 -0.11676431
A_23_P110167 -0.08502293
A_33_P3211513 -0.069378376
A_23_P103349 -0.008261204
A_32_P61480 -0.023947954
A_33_P3788124 -0.14432049
A_33_P3414202 0.28433895
A_33_P3316686 -0.14021635
A_33_P3300975 0.78603935
A_33_P3263061 0.77874374
A_33_P3261373 0.25157714

Total number of rows: 50739

Table truncated, full table size 1232 Kbytes.

Supplementary file Size Download File type/resource
GSM3754790_B1364.1.txt.gz 3.1 Mb (ftp)(http) TXT
Processed data included within Sample table
Processed data are available on Series record

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