NCBI Logo
GEO Logo
   NCBI > GEO > Accession DisplayHelp Not logged in | LoginHelp
GEO help: Mouse over screen elements for information.
          Go
Sample GSM2319645 Query DataSets for GSM2319645
Status Public on Sep 18, 2016
Title Female CP_sham_rep2
Sample type RNA
 
Source name Female choroid plexus_sham
Organism Rattus norvegicus
Characteristics strain: Wistar
tissue: choroid plexus
experimental procedure: Sham-operated
gender: Female
Treatment protocol Wistar rats were housed under a 12-h light, 12-h dark cycle, with food and water ad libitum during the course of the experiment. Female and male rats (2 months) were either ovariectomized or orchidectomized. Two weeks after surgery, castrated animals were anesthetized with a mixture of ketamine and medetomidine. Cerebral hemispheres were separated and both lateral ventricular CP removed and immediately frozen in liquid nitrogen
Extracted molecule total RNA
Extraction protocol Total RNA was extracted using TRIzol reagent (Invitrogen, Carlsbad, CA, USA) following manufacturer’s instructions. RNA was quantified using a NanoDrop spectrophotometer (NanoDrop Technologies), and RNA integrity was assessed by Bioanalyzer 2100 (Agilent Technologies, Santa Clara, CA, USA). All RNA samples used in this study had an A260/A280 ratio of.1.9
Label Cy3
Label protocol Pools of RNA samples from three animals were biological replicates. Equal amounts of RNA extract (200ng) from the 3 pools of sham or 3 pools of GDX animals, in a total of three biological replicates, were amplified and Cy-3-labeled using the Low Input Quick Amp Labeling kit (Agilent Technologies).
 
Hybridization protocol Hybridizations were carried out on an Agilent-based microarray platform using custom-designed whole genome Rat GE 4x4K v3 microarrays, and arrays were scanned with an Agilent microarray scanner (Agilent Technologies).
Scan protocol Scanned images were analyzed by Feature extraction software (Agilent Technologies) using GE1_105_Dec08 protocol.
Description CP gene expression in sham females
Data processing The signal intensity was normalized between microarrays by centering the median of the signal distribution using BRB-ArrayTools v3.8.1 (http://linus.nci.nih. gov/BRB-ArrayTools.html).
 
Submission date Sep 17, 2016
Last update date Sep 18, 2016
Contact name Telma Quintela
E-mail(s) [email protected]
Organization name University of Beira Interior
Department Health Sciences Research Centre
Street address Av. Infante D. Henrique
City Covilhã
ZIP/Postal code 6200-506
Country Portugal
 
Platform ID GPL14746
Series (1)
GSE87045 Sex hormone responsive genes in rat choroid plexus

Data table header descriptions
ID_REF
VALUE Normalized signal intensity

Data table
ID_REF VALUE
GE_BrightCorner 15.55007362
DarkCorner 2.14471674
A_64_P076162 1.683646798
A_64_P002176 7.304831505
A_42_P664913 10.32147408
A_43_P13320 1.580537796
A_64_P126523 5.645257473
A_64_P038045 6.334834576
A_43_P11804 10.42101002
A_44_P808710 12.37268353
A_64_P142111 11.04397774
A_64_P095642 8.543085098
A_42_P735279 14.31365013
A_44_P902822 7.281413078
A_42_P563843 1.698505998
A_42_P610788 9.317616463
A_44_P242429 11.33905983
A_64_P020571 9.003394127
A_42_P518462 13.92706108
A_42_P469751 13.57590675

Total number of rows: 30423

Table truncated, full table size 738 Kbytes.




Supplementary file Size Download File type/resource
GSM2319645_CPF06.txt.gz 2.1 Mb (ftp)(http) TXT
Processed data included within Sample table

| NLM | NIH | GEO Help | Disclaimer | Accessibility |
NCBI Home NCBI Search NCBI SiteMap