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Sample GSM3610007 Query DataSets for GSM3610007
Status Public on Feb 16, 2019
Title Right carotid-tPA-4days-Replicate1
Sample type RNA
 
Source name Wistar Kyoto rats common carotid arteries
Organism Rattus norvegicus
Characteristics strain/background: Wistar-Kyoto
gender: Male
age: 3 months
tissue: Right carotid
surgery: Balloon catheter injury of left carotid
treatment: tPA applied to left carotid
time point: 4 days
Treatment protocol Ketamine anesthesia was used (100 mg/kg body wt) and the balloon catheter (Fogarty 2F) injury of rats left common carotid arteries was performed. Following balloon catheter injury, 20 nmol/kg of recombinant tissue-type plasminogen activator dissolved in pluronic gel or 500 μl of plain Pluronic gel, F-127 (BASF) was applied to the adventitial side of the left common carotid arteries.
Extracted molecule total RNA
Extraction protocol For microarrays, 1 and 4 days after the operation carotids were rapidly removed and frozen in liquid nitrogen. Total RNA was extracted from carotid arteries of injured, sham-operated and intact rats.
Total RNA was isolated with the use of Qiagen RNeasy Micro kit, the quality of RNA was confirmed. For each probe vessels from 3 rats were pooled.
Label Biotin
Label protocol Labeled with biotin.
 
Hybridization protocol Microarray analysis was performed at the University of Rochester Microarray Core Facility in accordance to Affymetrix recommendations using Affymetrix rat genome U34A oligonucleotide microarrays with 8799 known genes and expressed sequence tags (ESTs) (Santa Clara, CA). Streptavidin phycoerythrin stain (SAPE, Molecular Probes) was used.
Scan protocol Target hybridization was detected and quantified with a Gene Array Scanner (Hewlett Packard/Affymetrix). “Array performance” was assessed. Hybridization efficiency and sensitivity were controlled using control transcripts spiked into the hybridization cocktail.
Description 3-month-old male Wistar-Kyoto rats.
Data processing Inter-array variability was assessed by Microarray Analysis Suite 5.0. For data normalization global scaling with target intensity of 500 across all probe sets was used.
 
Submission date Feb 15, 2019
Last update date Feb 16, 2019
Contact name Olga Plekhanova
Organization name Lomonosov Moscow State University
Street address Lomonosovsky prospect, 27-1
City Moscow
ZIP/Postal code 119991
Country Russia
 
Platform ID GPL85
Series (1)
GSE126627 Oligonucleotide Microarrays Identified Potential Regulatory Genes Related To Early Outward Arterial Remodeling Induced By Tissue Plasminogen Activator

Data table header descriptions
ID_REF
VALUE MAS5.0 signal intensity

Data table
ID_REF VALUE
AFFX-MurIL2_at 11
AFFX-MurIL10_at 16.5
AFFX-MurIL4_at 3.9
AFFX-MurFAS_at 8.3
AFFX-BioB-5_at 47.9
AFFX-BioB-M_at 31.6
AFFX-BioB-3_at 117.6
AFFX-BioC-5_at 1117.6
AFFX-BioC-3_at 838.1
AFFX-BioDn-5_at 918.5
AFFX-BioDn-3_at 3509.6
AFFX-CreX-5_at 4652.3
AFFX-CreX-3_at 4692.7
AFFX-BioB-5_st 101.2
AFFX-BioB-M_st 45.6
AFFX-BioB-3_st 30
AFFX-BioC-5_st 16.5
AFFX-BioC-3_st 8.3
AFFX-BioDn-5_st 13.5
AFFX-BioDn-3_st 19.7

Total number of rows: 8799

Table truncated, full table size 161 Kbytes.




Supplementary file Size Download File type/resource
GSM3610007_30_Berk_S2_U34A.CEL.gz 2.4 Mb (ftp)(http) CEL
Processed data included within Sample table

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