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Sample GSM3111025 Query DataSets for GSM3111025
Status Public on Jun 03, 2018
Title 757-2010--0DIV
Sample type RNA
 
Source name Hippocampal neurons, 0DIV, replicate 1
Organism Mus musculus
Characteristics time: 0 days
replicate: B
Treatment protocol No treatments were performed
Growth protocol Pregnant RjOrl:SWISS female mice were purchased from Janvier Labs. Hippocampal and cortical cell cultures were prepared from e17.5-18.5 mouse embryos. Briefly, hippocampi were dissected,treated with 0.25% trypsin (Life Technologies) during 15 min at 37ºC and dissociated into single cells by gentle trituration. Neurons were seeded on glass coverslips or plastic plates coated with 0.1 mg/ml Poly-D-lysine (Sigma) at ~105 cells/cm2 or 2x104 cells/cm2 for low-density cultures. Neurons were plated in DMEM containing 10% fetal bovine serum (FBS), penicillin/streptomycin (pen/strep), and 1-2 hours later medium was replaced by Neurobasal medium supplemented with 2% B27, pen/strep, 0.6% Glucose and Glutamax (all reagents from Life Technologies). Cytosine arabinoside (1 µM; Sigma) was added to cultures at 3 days in vitro (DIV) and 1/3 of the medium was refreshed every 4-5 days
Extracted molecule total RNA
Extraction protocol RNA was prepared using the QIAGEN Rneasy Mini Kit - Total RNA Purification kit following the manufacturers instructions
Label biotin
Label protocol 25 ng total RNA was amplified using the TransPlex® Complete Whole Transcriptome Amplification Kit (Sigma; reference WTA2) and 8 µg of cDNA was subsequently fragmented and labeled using GeneChip Mapping 250K Nsp Assay Kit (Affymetrix; catalog # 900766), according to manufacturer's instructions.
 
Hybridization protocol cDNA was hybridized to the microarray for 16 hours at 45ºC, washing and staining of microarrays was performed using a GeneChip Fluidics Station 450 (Affymetrix, Santa Clara, CA)
Scan protocol Arrays were scanned with GeneChip scanner GSC3000 (Affymetrix, Santa Clara, CA)
Description Gene expression at 0DIV in cultured mouse hippocampal neurons
Data processing Normalized expression signals were calculated from Affymetrix CEL files using RMA algorithm (Irizarry et al., 2003)
 
Submission date Apr 25, 2018
Last update date Jun 03, 2018
Contact name Camille Stephan Otto Attolini
Organization name IRB Barcelona
Department Biostatistics and bioinformatics Unit
Street address Baldiri Reixac 10
City Barcelona
State/province Select a State or Province
ZIP/Postal code 08028
Country Spain
 
Platform ID GPL10740
Series (1)
GSE113680 Gene expression signatures during differentiation of mouse hippocampal neurons in primary culture

Data table header descriptions
ID_REF
VALUE log2 RMA expression estimate

Data table
ID_REF VALUE
10338001 12.3922541863538
10338002 6.37404201817916
10338003 10.5944711221389
10338004 10.1919774111518
10338005 3.26479581361575
10338006 3.46604981004912
10338007 3.79967041455937
10338008 4.38111564739153
10338009 7.47686659149042
10338010 3.28902721874858
10338011 5.99179975426477
10338012 3.36455889814494
10338013 3.14281934097154
10338014 3.18175999942918
10338015 3.1535957421193
10338016 7.23351029065932
10338017 12.9313787987032
10338018 6.70388257799677
10338019 5.50020849223529
10338020 7.67195685189837

Total number of rows: 241576

Table truncated, full table size 6107 Kbytes.




Supplementary file Size Download File type/resource
GSM3111025_CLSept10--757-2010--0DIV_MoGene-1_0-st-v1_.CEL.gz 4.2 Mb (ftp)(http) CEL
Processed data included within Sample table

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