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Sample GSM2385138 Query DataSets for GSM2385138
Status Public on Nov 06, 2018
Title Con_168
Sample type RNA
 
Source name Peripheral blood from control subject
Organism Homo sapiens
Characteristics diagnosis: control
tissue: whole blood
age: 22y
gender: male
Extracted molecule total RNA
Extraction protocol miRNA was extracted from peripheral blood of participants by using the PAXgene Blood miRNA System (QIAGEN, Tokyo, Japan) following the manufacturer's protocol with DNase treatment step. RNA was quantified using a NanoDrop-2000 spectrophotometer (Thermo Fisher Scientific, Yokohama, Japan), and quality was determined by the Agilent 2100 Bioanalyzer (Agilent Technologies, Tokyo, Japan).
Label Cy3
Label protocol Following manufacturer's instructions, total RNA (100ng) was labeled with Cy3 using the miRNA Complete Labeling and Hyb Kit(Agilent Technologies, Tokyo, Japan).
 
Hybridization protocol Following manufacturer's instructions, labelled RNA was hybridized to the SurePrint G3 Human miRNA 8x60K Microarray (G4870C) (Agilent Technologies) using the miRNA Complete Labeling and Hyb Kit (Agilent Technologies). Hybridization step was performed for 20 hours at 55°C at a constant speed rotation of 20rpm. After hybridization, microarrays were washed 5 minute at room temperature with GE Wash Buffer 1 (Agilent Technologies) and 5 minute with 37°C GE Wash buffer 2 (Agilent Technologies), then dried immediately by brief centrifugation.
Scan protocol Slides were scanned immediately after washing on Agilent Microarray Scanner(p/n G2565BA) using one color scan setting for 8x60k array slides (Scan Area 61x21.6 mm, Scan resolution 3um, Dye channel is set to Green and Green PMT is set to 100%).
Data processing The scanned images were analyzed with Feature Extraction Software 11.0.1.1 (Agilent Technologies) using default parameters (protocol: miRNA_1100_Jul11 and Grid: 070156_D_F_20141006) to obtain background subtracted and spatially detrended Processed Signal intensities.
 
Submission date Nov 07, 2016
Last update date Nov 06, 2018
Contact name Ryo Kimura
E-mail(s) [email protected]
Organization name Kyoto University Graduate School of Medicine
Department Anatomy and Developmental Biology
Street address Yoshida-Konoe-cho
City Kyoto
ZIP/Postal code 606-8501
Country Japan
 
Platform ID GPL21575
Series (1)
GSE89595 Signiture microRNA expression patterns identified in Williams syndrome

Data table header descriptions
ID_REF
VALUE Normalized signal intensity in log2 scale, using the “AgiMicroRna” software package (version 3.3.1).

Data table
ID_REF VALUE
1 297.14
2 -28.78
3 -32.08
4 -30.20
5 -32.58
6 -31.93
7 -31.19
8 -29.73
9 -32.27
10 -28.13
11 -6.93
13 -7.26
14 1.64
15 -4.57
16 -0.73
17 1.74
18 -4.17
21 -4.16
23 1.09
24 -10.37

Total number of rows: 53144

Table truncated, full table size 605 Kbytes.




Supplementary file Size Download File type/resource
GSM2385138_MA52_C.txt.gz 2.8 Mb (ftp)(http) TXT
Processed data included within Sample table

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