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Sample GSM3610005 Query DataSets for GSM3610005
Status Public on Feb 16, 2019
Title Left carotid-Gel-4days-Replicate2
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: Left carotid
surgery: Balloon catheter injury of left carotid
treatment: Gel 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 11.6
AFFX-MurIL10_at 11
AFFX-MurIL4_at 2.4
AFFX-MurFAS_at 11.5
AFFX-BioB-5_at 30.5
AFFX-BioB-M_at 110.9
AFFX-BioB-3_at 93.4
AFFX-BioC-5_at 1136.4
AFFX-BioC-3_at 600.4
AFFX-BioDn-5_at 705.2
AFFX-BioDn-3_at 3455.1
AFFX-CreX-5_at 4265.3
AFFX-CreX-3_at 5122
AFFX-BioB-5_st 92.7
AFFX-BioB-M_st 76.9
AFFX-BioB-3_st 25.1
AFFX-BioC-5_st 18.7
AFFX-BioC-3_st 10
AFFX-BioDn-5_st 9.3
AFFX-BioDn-3_st 18.2

Total number of rows: 8799

Table truncated, full table size 160 Kbytes.




Supplementary file Size Download File type/resource
GSM3610005_11_Berk_S2_U34A.CEL.gz 2.4 Mb (ftp)(http) CEL
Processed data included within Sample table

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