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Sample GSM1259970 Query DataSets for GSM1259970
Status Public on Nov 15, 2013
Title DL nucleus motor neurons bio rep 2
Sample type RNA
 
Source name motor neurons laser captured from sections of dorsolateral nucleus at L6 level of the spinal cord of P7 male mouse
Organism Mus musculus
Characteristics strain: C57BL/6J
gender: male
age: postnatal day 7
cell type: DL nucleus motor neurons
Treatment protocol none
Growth protocol Mice were obtained from Jackson Labs and were housed under standerd condicition as per IACUC protocol.
Extracted molecule total RNA
Extraction protocol Postnatal day 7 male animals were perfused with 30% sucrose, lumbosacral spinal cord and midbrain regions were rapidly recovered, embedded in OCT compound, and frozen in liquid nitrogen. 12 µm-thick cryosections were mounted on RNAse-free, PEN-foil covered glass slides (Zeiss), fixed for 2 min in 100% EtOH, rinsed in 50% EtOH, stained with 1% cresyl violet for 2 min, rinsed with 50% EtOH, dehydrated in graded solutions of ethanol and air dried prior to LCM using PALM Microbeam system. From each animal, ~200 DL, L5, and oculomotor motor neurons were collected directly in lysis buffer. RNA was purified using Absolutely RNA, NanoPrep kit. RNA integrity was assessed on the Bioanalyzer 2100.
Label biotin
Label protocol At least 1.5 ng of purified RNA was the starting material used in the WT-Ovation Pico RNA Amplification System (Nugen, San Carlos,CA) with the FL-Ovation cDNA Biotin Module V2 (Nugen) to generate labeled probe.
 
Hybridization protocol µg of biotinylated cRNA from three independent samples for each motor neuron group isolated by LCM was hybridized to on Affymetrix Mouse Genome 430 2.0 Arrays.
Scan protocol Arrays were scanned on an Affymetrix Scanner 3000-7G scanner with GCOS software. Scanning was peformed according to the protocol described in the Affymetrix GeneChip® Expression Analysis Technical Manual, November 2004 Edition
Description gene expression data from dorsolateral nucleus motor neurons of young wild type mouse
Data processing GeneSpring and BioconductorLIMMA package was used for statistical analysis
 
Submission date Nov 05, 2013
Last update date Nov 15, 2013
Contact name Krista Joan Spiller
E-mail(s) [email protected]
Organization name Columbia University
Street address 630 W 168th street
City New York
State/province New York
ZIP/Postal code 10032
Country USA
 
Platform ID GPL1261
Series (1)
GSE52118 Comparison of gene expression in motor pools with differential vulnerability in ALS

Data table header descriptions
ID_REF
VALUE MAS 5.0 signal
ABS_CALL
DETECTION P-VALUE

Data table
ID_REF VALUE ABS_CALL DETECTION P-VALUE
AFFX-BioB-5_at 14667.4 P 0.000044
AFFX-BioB-M_at 18267.4 P 0.000044
AFFX-BioB-3_at 16476.4 P 0.000044
AFFX-BioC-5_at 26201 P 0.000044
AFFX-BioC-3_at 17426.3 P 0.000044
AFFX-BioDn-5_at 30142.8 P 0.000044
AFFX-BioDn-3_at 28967.1 P 0.000044
AFFX-CreX-5_at 33740.3 P 0.000044
AFFX-CreX-3_at 35872.4 P 0.000044
AFFX-DapX-5_at 0.9 A 0.904352
AFFX-DapX-M_at 1.7 A 0.94983
AFFX-DapX-3_at 14.8 A 0.131361
AFFX-LysX-5_at 1.3 A 0.93239
AFFX-LysX-M_at 4.5 A 0.659352
AFFX-LysX-3_at 0.5 A 0.992384
AFFX-PheX-5_at 0.9 A 0.98746
AFFX-PheX-M_at 2.2 A 0.804754
AFFX-PheX-3_at 15.4 A 0.123572
AFFX-ThrX-5_at 1.1 A 0.932322
AFFX-ThrX-M_at 3.8 A 0.631573

Total number of rows: 45101

Table truncated, full table size 1196 Kbytes.




Supplementary file Size Download File type/resource
GSM1259970_DL_2.CEL.gz 3.2 Mb (ftp)(http) CEL
Processed data included within Sample table

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