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Status |
Public on Nov 15, 2013 |
Title |
DL nucleus motor neurons bio rep 1 |
Sample type |
RNA |
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|
Source name |
motor neurons laser captured from sections of dorsolateral nucleus at L6 level of the spinal cord of P7 male mouse
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Organism |
Mus musculus |
Characteristics |
strain: C57BL/6J gender: male age: postnatal day 7 cell type: DL nucleus motor neurons
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Treatment protocol |
none
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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.
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|
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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.
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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
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Description |
gene expression data from dorsolateral nucleus motor neurons of young wild type mouse
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Data processing |
GeneSpring and BioconductorLIMMA package was used for statistical analysis
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|
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Submission date |
Nov 05, 2013 |
Last update date |
Nov 15, 2013 |
Contact name |
Krista Joan Spiller |
E-mail(s) |
[email protected]
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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 |
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