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Sample GSM1306233 Query DataSets for GSM1306233
Status Public on Jun 16, 2014
Title OGD 7h_R1
Sample type RNA
 
Source name Oxygen and Glucose Deprivation 7h_R1
Organism Rattus norvegicus
Characteristics strain background: Wistar
develpmetal stage: E18 rat embryos
tissue: Primary hippocampal neurons
exposed to: Oxygen and Glucose deprivation (OGD)
time point: after 7h recovery
Treatment protocol For the OGD challenge, hippocampal cultures were incubated in a glucose-free saline buffer (in mM: 10 HEPES, 116 NaCl, 5.4 KCl, 0.8 MgSO4, 1 NaH2PO4, 1.8 CaCl2, 25 NaHCO3, 25 sucrose, pH 7.3) in an anaerobic chamber (Forma Anaerobic System, Thermo Fisher Scientific), at 37C, for the indicated times. Control neurons were placed in a similar saline buffer with 25 mM glucose instead of sucrose and kept in an air/CO2 incubator, at 37C, for the same period of time. After the stimulus periods, the saline buffers were replaced by conditioned medium and the cultures returned to the air/CO2 incubator, where they were kept to recover for the indicated times.
Growth protocol The cultures were maintained in Neurobasal medium in a humidified incubator with 5% CO2/95% air, at 37°C, for 14-15 days.
Extracted molecule total RNA
Extraction protocol Total RNA from three rat hippocampal neuronal cultures submitted to control or OGD conditions were collected after 7h and 24h of recovery
Label Cy3
Label protocol Equal amounts of RNA extract (200 ng) from each replicate were amplified and Cy-3-labeled using the Low Input Quick Amp Labeling kit (Agilent Technologies)
 
Hybridization protocol Hybridizations were carried out following Agilent Technologies instructions for One-Color Microarray-Based Gene Expression Analysis (Agilent Technologies, Santa Clara, CA, USA), using whole-genome Rat GE 4x44K v3 Microarrays.
Scan protocol Images were obtained using Agilent G2565AA microarray scanner and fluorescence quantization was performed using Agilent Feature Extraction 10.5.1.1 software and GE1_105_Dec08 protocol.
Description Gene expression of OGD-stimulated neurons after 7h
Data processing The signal intensity was aligned and normalized between microarrays by centering the median of the signal distribution using BRB-ArrayTools v3.8.1.
 
Submission date Jan 13, 2014
Last update date Jun 16, 2014
Contact name Joana Filipa Fernandes
E-mail(s) [email protected]
Organization name Center for Neuroscience and Cell Biology
Department Life Sciences
Lab Neurobiology and Disease
Street address Rua Larga, Faculdade de Medicina 2º andar, lab 206A Coimbra
City Coimbra
State/province -- Please Select --
ZIP/Postal code 3004-504
Country Portugal
 
Platform ID GPL14746
Series (1)
GSE54037 In vitro ischemia triggers a transcriptional response to down-regulate synaptic proteins in hippocampal neurons.

Data table header descriptions
ID_REF
VALUE Normalized signal intensity

Data table
ID_REF VALUE
GE_BrightCorner 15.75011253
DarkCorner 2.424855232
A_64_P076162 2.540240765
A_64_P002176 6.024099827
A_42_P664913 9.57809639
A_43_P13320 2.423977852
A_64_P126523 6.431677341
A_64_P038045 6.829265594
A_43_P11804 13.94546127
A_44_P808710 5.145925999
A_64_P142111 10.40379524
A_64_P095642 8.694038391
A_42_P735279 12.1184597
A_44_P902822 6.671355247
A_42_P563843 2.225545883
A_42_P610788 12.65501785
A_44_P242429 9.180082321
A_64_P020571 8.004915237
A_42_P518462 12.43935776
A_42_P469751 4.817877769

Total number of rows: 30423

Table truncated, full table size 738 Kbytes.




Supplementary file Size Download File type/resource
GSM1306233_UA_252828210541_OGD_7h_R1.txt.gz 2.1 Mb (ftp)(http) TXT
Processed data included within Sample table

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