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Sample GSM3111032 Query DataSets for GSM3111032
Status Public on Jun 03, 2018
Title 682-2010--20h01
Sample type RNA
 
Source name Hippocampal neurons, 1DIV, replicate 2
Organism Mus musculus
Characteristics time: 20 hours
replicate: A
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 1DIV 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 5.95889207750541
10338002 6.17940312821532
10338003 6.24776062305923
10338004 6.43590836485955
10338005 3.15195965232594
10338006 3.33361148405627
10338007 3.60247253745529
10338008 4.1710251380469
10338009 6.8422613257021
10338010 3.19135547552668
10338011 5.77217011186614
10338012 3.25222198822434
10338013 3.04589931151811
10338014 3.09469398125746
10338015 3.05796038153987
10338016 6.84348438082218
10338017 4.49218465601799
10338018 6.45492060615228
10338019 5.30004507386017
10338020 7.19290438727894

Total number of rows: 241576

Table truncated, full table size 6106 Kbytes.




Supplementary file Size Download File type/resource
GSM3111032_JLAug10--682-2010--20h01.CEL.gz 4.7 Mb (ftp)(http) CEL
Processed data included within Sample table

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