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Sample GSM3111030 Query DataSets for GSM3111030
Status Public on Jun 03, 2018
Title 763-2010--15DIV
Sample type RNA
 
Source name Hippocampal neurons, 15DIV, replicate 1
Organism Mus musculus
Characteristics time: 15 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 15DIV 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 11.4522563245986
10338002 7.2216169643665
10338003 9.58582964981432
10338004 8.94917046852591
10338005 3.24324885269078
10338006 3.53799793945415
10338007 4.0848741373297
10338008 4.89797567540587
10338009 8.40424991594103
10338010 3.27759029060908
10338011 6.80353613481282
10338012 3.41006137796825
10338013 3.11739083081165
10338014 3.16835763927477
10338015 3.11994112827649
10338016 8.10279872182181
10338017 11.7620908894434
10338018 7.61626677789524
10338019 6.27570971144956
10338020 8.62304306657102

Total number of rows: 241576

Table truncated, full table size 6106 Kbytes.




Supplementary file Size Download File type/resource
GSM3111030_CLSept10--763-2010--15DIV_MoGene-1_0-st-v1_.CEL.gz 4.4 Mb (ftp)(http) CEL
Processed data included within Sample table

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