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Sample GSM1001333 Query DataSets for GSM1001333
Status Public on Nov 17, 2015
Title Veh 1
Sample type RNA
 
Source name rat hearts
Organism Rattus norvegicus
Characteristics tissue: Heart
strain: Sprague-Dawley
gender: Male
treatment: exposed to vehicle
Treatment protocol Diabetes mellitus was induced in Sprague-Dawley rats by a single injection of streptozotocin (STZ; 60 mg/kg) into the tail vein. The plasma glucose concentration in the rats was > 300 mg/dL and they were assigned to groups with diabetes mellitus and with DM and plasma glucose fluctuations induced by 24 hours of starvation and intraperitoneal insulin (0.5 IU/kg) injection.
Extracted molecule total RNA
Extraction protocol Total RNA from rat heart was extracted with a miRNeasy Mini kit (QIAGEN) following the manufacturer's instructions. RNA was quantified using a NanoDrop-1000 spectrophotometer.
Label Cy3
Label protocol One hundred ng of total RNA was labeled with Cy3 using a miRNA labeling and hybridization kit (Agilent Technologies) according to the manufacturer’s instructions.
 
Hybridization protocol After Cy3-labeling, RNA was dried up and re-solved with 18 ul RNase-free water. And then, 4.5 ul of 10x Gene expression blocking agent and 22.5 ul of 2x hybridization buffer HI-RPM were added to the RNA sample, and the mixture hybridized to Agilent rat miRNA Microarrays (Grid ID19159, Rat Rel. 10.1, Agilent Technologies) for 20 hours at 55°C in a rotating Agilent hybridization oven. 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).
Scan protocol Slides were scanned immediately after washing on the Agilent DNA Microarray Scanner (G2565BA) using one color scan setting for 8x15k array slides (Scan Area 61x21.6 mm, Scan resolution 5um, Dye channel is set to Green and Green PMT is set to 5% and 100%, extended dynamic range scan mode).
Description miRNA expression in the heart of control rat
Data processing The scanned images were analyzed with Feature Extraction Software 9.5.3.1 (Agilent Technologies) using default parameters (protocol miRNA-v1_95_May07 and Grid: 019159_D_20081121) to obtain background subtracted Processed Signal intensities. Features flagged in Feature Extraction as Feature Non-uniform outliers were excluded.
 
Submission date Sep 11, 2012
Last update date Nov 17, 2015
Contact name Yasushi Teshima
Organization name Oita University
Street address 1-1 Idaigaoka, Yufu
City Oita
ZIP/Postal code 8700026
Country Japan
 
Platform ID GPL10344
Series (1)
GSE40779 The expression profiles of miRNAs in the heart with glucose fluctuation compared with sustained hyperglycemia.

Data table header descriptions
ID_REF
VALUE Normalized signal intensity

Data table
ID_REF VALUE
rno-miR-434 -0.30602407
rno-miR-27a -0.13608932
rno-miR-186 -0.2866583
rno-miR-30c-2* -0.2988801
rno-miR-333_v11.0 -0.51768327
rno-let-7b -0.25274754
rno-miR-674-5p -0.14251915
rno-miR-301b 0
rno-let-7e* -0.6315037
rno-miR-345-5p -0.17460823
rno-miR-148b-3p -0.2702961
rno-miR-34c 0.020450115
rno-miR-463 0
rno-miR-497 -0.24963284
rno-miR-125b-5p -0.286129
rno-miR-7a -0.33101368
rno-miR-151 -0.09229851
rno-miR-23a* 0
rno-miR-448 0
rno-miR-409-5p 0

Total number of rows: 350

Table truncated, full table size 7 Kbytes.




Supplementary file Size Download File type/resource
GSM1001333_Veh_1_US45102856_251915910468_S01_miRNA-v1_95_May07_1_1.txt.gz 412.2 Kb (ftp)(http) TXT
Processed data included within Sample table
Processed data provided as supplementary file

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