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Sample GSM4288671 Query DataSets for GSM4288671
Status Public on Aug 23, 2020
Title AD52_Hip_rep7
Sample type RNA
 
Source name AD52 Hip rep7
Organism Mus musculus
Characteristics strain: 3xTg-AD
tissue: hippocampus
age: 52 weeks
Treatment protocol Mice at 12 or 52 w.o.a. were anesthetized and killed by decapitation. Hippocampi were immediately stored, and bloods were collected in RNeasy Protect Animal Blood Tube (QIAGEN, #73224) and stored at -80℃ for RNA processing.
Growth protocol The 3xTg-AD male mice (n=8 at 12 w.o.a; n=8 at 52 w.o.a) and age-matched B6129SF2 WT male mice (n=8 at 12 w.o.a; n=8 at 52 w.o.a) were bred at Ehime University from parents originally purchased from Jackson Laboratory (Bar Harbor, ME, USA, 3xTG-AD, MMRRC #34830; B6129SF1/J, JAX #101043) in a specific pathogen-free facility under climate-controlled conditions at room temperature (22 +/- 2 ℃) with 50% humidity and a 12-h light/dark cycle. Mice were provided with water and standard diet (MF, Oriental Yeast Co. Ltd.) at libitum.
Extracted molecule total RNA
Extraction protocol Total RNA was extracted from frozen hippocampi using RNeasy Mini Kit (QIAGEN, #74104) and from blood using RNeasy Protect Animal Blood Kit (QIAGEN, #73224) according to the manufacturer instructions.
Label Cy3
Label protocol RNA (50ng) was used for microarray analysis. The Low Input Quick Amp Labeling Kit (Agilent) was used to generate amplified and biotinylated sense-strand DNA targets.
 
Hybridization protocol Hybridization, washing and scanning steps with SurePrint G3 Mouse 8x60K ver.2.0 were conducted using Gene Expression Hybridization Kit (Agilent), Gene Expression Wash Pack (Agilent, #5188-5327) and Agilent Microarray Scanner (G2505C).
Scan protocol Hybridization, washing and scanning steps with SurePrint G3 Mouse 8x60K ver.2.0 were conducted using Gene Expression Hybridization Kit (Agilent), Gene Expression Wash Pack (Agilent, #5188-5327) and Agilent Microarray Scanner (G2505C).
Description Hippocampal gene expression at 52 week
Data processing The 75th percentile shift normalization and baseline transformation(baseline to median of all samples (all bloods or all hippocampi)) were performed using Agilent GeneSpring GX ver 14.9.
 
Submission date Jan 29, 2020
Last update date Aug 24, 2020
Contact name Junichi Iga
E-mail(s) igajunichi@hotmail.com
Organization name Ehime University
Department Neuropsychiatry
Street address Shitsukawa 454
City Toon
State/province Ehime
ZIP/Postal code 7910295
Country Japan
 
Platform ID GPL21163
Series (1)
GSE144459 Identifying blood transcriptome biomarkers of Alzheimer’s disease using transgenic mice

Data table header descriptions
ID_REF
VALUE Normalized signal intensity

Data table
ID_REF VALUE
GE_BrightCorner 0.7657
DarkCorner 1.0492
A_51_P399985 1.0837
A_55_P2508138 0.9518
A_55_P2805880 5.4938
A_55_P2419483 1.0534
A_55_P2739683 1.0226
A_51_P211903 1.1180
A_66_P121325 1.0088
A_51_P226429 1.1658
A_55_P2841743 1.0609
A_55_P2737159 1.0015
A_55_P2728466 1.1368
A_55_P2101526 0.9667
A_52_P1132414 0.9929
A_66_P135936 0.9981
A_55_P2805396 0.9119
A_55_P2717104 0.6877
A_55_P2909714 0.9301
A_55_P2744310 1.5132

Total number of rows: 56745

Table truncated, full table size 1140 Kbytes.




Supplementary file Size Download File type/resource
GSM4288671_US82800151_257480915250_S01_GE1_1200_Jun14_2_3.txt.gz 12.5 Mb (ftp)(http) TXT
Processed data included within Sample table

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