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Sample GSM1259971 Query DataSets for GSM1259971
Status Public on Nov 15, 2013
Title DL nucleus motor neurons bio rep 3
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 9814.4 P 0.000044
AFFX-BioB-M_at 11744.7 P 0.000044
AFFX-BioB-3_at 9754.4 P 0.000044
AFFX-BioC-5_at 15744.4 P 0.000044
AFFX-BioC-3_at 11017.9 P 0.000044
AFFX-BioDn-5_at 18776.1 P 0.000044
AFFX-BioDn-3_at 17145.3 P 0.000044
AFFX-CreX-5_at 21092.1 P 0.000044
AFFX-CreX-3_at 21117.8 P 0.000044
AFFX-DapX-5_at 1.4 A 0.834181
AFFX-DapX-M_at 1.3 A 0.988616
AFFX-DapX-3_at 13.9 A 0.131361
AFFX-LysX-5_at 2 A 0.617411
AFFX-LysX-M_at 2.4 A 0.772364
AFFX-LysX-3_at 0.9 A 0.945802
AFFX-PheX-5_at 1.5 A 0.932339
AFFX-PheX-M_at 1.6 A 0.749204
AFFX-PheX-3_at 4.8 A 0.48511
AFFX-ThrX-5_at 1.6 A 0.876428
AFFX-ThrX-M_at 0.7 A 0.860538

Total number of rows: 45101

Table truncated, full table size 1195 Kbytes.




Supplementary file Size Download File type/resource
GSM1259971_DL_1.CEL.gz 3.3 Mb (ftp)(http) CEL
Processed data included within Sample table

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