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Status |
Public on Oct 30, 2009 |
Title |
Adult Sham; Biological replicate 6 |
Sample type |
RNA |
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|
Source name |
Rat spinal dorsal horn
|
Organism |
Rattus norvegicus |
Characteristics |
strain: Sprague-Dawley tissue: spinal cord (ipsilateral dorsal horn) developmental stage: Adult (8-12wks) treatment group: sham
|
Treatment protocol |
SNI surgery was performed where the tibial and common peroneal branches of the sciatic nerve were tightly ligated with a silk suture and transected distally, while the sural nerve was left intact (Decosterd and Woolf, 2000). In sham-operated controls, the sciatic nerve was exposed but not ligated. Operation performed under isofluorane.
|
Growth protocol |
Standard laboratory rodent housing, with free access to water and food and were exposed to a 12:12 hour on/off light cycle. Pups left with mothers following surgery.
|
Extracted molecule |
total RNA |
Extraction protocol |
Trizol extraction of total RNA.
|
Label |
Biotin
|
Label protocol |
Biotinylated cRNA were prepared according to the standard Affymetrix protocol from 5 ug total RNA.
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|
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Hybridization protocol |
Following fragmentation, 10 ug of cRNA were hybridized for 16 hr at 45C on GeneChip Drosophila Genome Array. GeneChips were washed and stained in the Affymetrix Fluidics Station 400.
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Scan protocol |
GeneChips were scanned using the Hewlett-Packard GeneArray Scanner G2500A.
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Description |
Global gene expression
|
Data processing |
The Bioconductor affy library was used to import CEL file data and the gcrma library was used to normalize the raw data.
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Submission date |
Oct 29, 2009 |
Last update date |
Oct 29, 2009 |
Contact name |
Caroline Emma Johnston |
E-mail(s) |
caroline.johnston@iop.kcl.ac.uk
|
Organization name |
Kings College London
|
Street address |
125 Coldharbour Lane
|
City |
London |
ZIP/Postal code |
SE5 9NU |
Country |
United Kingdom |
|
|
Platform ID |
GPL341 |
Series (1) |
GSE18803 |
Adult and Neonatal dorsal horn gene expression 7 day post sciatic nerve SNI injury |
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