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Sample GSM1259963 Query DataSets for GSM1259963
Status Public on Nov 15, 2013
Title lumbar motor neurons bio rep 1
Sample type RNA
 
Source name motor neurons laser captured from sections of L5 levesl of the spinal cord of P7 male mouse
Organism Mus musculus
Characteristics strain: C57BL/6J
gender: male
age: postnatal day 7
cell type: lumbar 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 lumbar motor neurons of young wildtype 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 18307.3 P 0.000044
AFFX-BioB-M_at 19653.2 P 0.000044
AFFX-BioB-3_at 17401.5 P 0.000044
AFFX-BioC-5_at 29365.9 P 0.000044
AFFX-BioC-3_at 18718.8 P 0.000044
AFFX-BioDn-5_at 35199 P 0.000044
AFFX-BioDn-3_at 32395.4 P 0.000044
AFFX-CreX-5_at 41459 P 0.000044
AFFX-CreX-3_at 38888.8 P 0.000044
AFFX-DapX-5_at 0.8 A 0.921998
AFFX-DapX-M_at 1.7 A 0.852145
AFFX-DapX-3_at 2.8 A 0.749223
AFFX-LysX-5_at 2.4 A 0.904333
AFFX-LysX-M_at 1.7 A 0.904352
AFFX-LysX-3_at 1.8 A 0.876448
AFFX-PheX-5_at 1.1 A 0.852061
AFFX-PheX-M_at 7.4 A 0.588627
AFFX-PheX-3_at 12 A 0.239063
AFFX-ThrX-5_at 2.5 A 0.794288
AFFX-ThrX-M_at 0.5 A 0.997725

Total number of rows: 45101

Table truncated, full table size 1198 Kbytes.




Supplementary file Size Download File type/resource
GSM1259963_L_3.CEL.gz 3.1 Mb (ftp)(http) CEL
Processed data included within Sample table

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