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Sample GSM7324416 Query DataSets for GSM7324416
Status Public on Apr 30, 2024
Title CD11brGFP-CTL-1
Sample type RNA
 
Source name CD11brGFP mice; n=6
Organism Mus musculus
Characteristics genotype: CD11brGFP transgenic
treatment: Sham operated animals
fraction: Ribosomes-associated mRNAs
Treatment protocol CD11brGFP transgenic mice were subjected to tMCAO-24hrs. Each group contains 6 mice with only males. Three biological replicates were used for control and for tMCAO-24hrs.
Growth protocol CD11brGFP transgenic mice were used at 2-3 months old.
Extracted molecule total RNA
Extraction protocol mRNA was extracted using the Translational Affinity Purification (TRAP) protocol. The purification of the mRNA from the beads was perfomed according to the Absolutely RNA Nanoprep Kit's instructions
Label Biotin
Label protocol Ribosomes-associated mRNA (100 ng per sample) was labeled using the Affymetrix GeneChip® WT cDNA Synthesis and Amplification Kit protocol as described by the manufacturer (Affymetrix).
 
Hybridization protocol Samples were hybridized with Affymetrix Mouse Gene 2.0 ST microarray. The cRNA hybridization cocktail was incubated overnight at 45°C while rotating in a hybridization oven. After 16 h of hybridization, the cocktail was removed and the arrays were washed and stained in an Affymetrix GeneChip fluidics station 450, according to the Affymetrix-recommended protocol.
Scan protocol The arrays were scanned using the Affymetrix GCS 3000 7G and the Gene-Chip Command Console Software (AGCC) (Affymetrix, Santa Clara, CA) to produce the probe cell intensity data (CEL). The image data were analyzed by using the Affymetrix Expression Console Software to perform the quality control, the background subtraction and the normalization of probe set intensities with the method of Robust Multiarray Analysis (RMA).
Data processing For the visualization of microarray results we used Affymetrix Transcriptome Analysis Console (TAC) Software. A mRNA was considered as variant if the fold change between the two compared samples was higher than 1.2 and the associated ANOVA p-value was lower than 0.05.
 
Submission date May 11, 2023
Last update date Apr 30, 2024
Contact name Hejer Boutej
E-mail(s) hajer.boutej.1@ulaval.ca
Organization name LAVAL University
Department NEUROBIOLOGY
Lab CERVO
Street address 2601, de la Canardière
City Québec
State/province Québec
ZIP/Postal code G1J 2G3
Country Canada
 
Platform ID GPL16570
Series (1)
GSE232244 Differential Expression Data from Mice 24hrs after stroke

Data table header descriptions
ID_REF
VALUE RMA signal

Data table
ID_REF VALUE
17200001 5.36504
17200003 5.0955
17200005 3.11017
17200007 4.8162
17200009 4.33995
17200011 3.26342
17200013 5.46743
17200015 5.06039
17200017 3.54421
17200019 2.16441
17200021 2.96996
17200023 5.06007
17200025 4.95244
17200027 5.62208
17200029 1.95777
17200031 3.45526
17200033 4.20964
17200035 2.44507
17200037 5.2386
17200039 3.2869

Total number of rows: 41345

Table truncated, full table size 681 Kbytes.




Supplementary file Size Download File type/resource
GSM7324416_JK-1_Ctrl-1_MoGene-2_0-st_.CEL.gz 9.5 Mb (ftp)(http) CEL
GSM7324416_JK-1_Ctrl-1_MoGene-2_0-st_.rma-gene-full.chp.gz 254.6 Kb (ftp)(http) CHP
Processed data included within Sample table
Processed data provided as supplementary file
Processed data are available on Series record

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