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Status |
Public on Feb 09, 2007 |
Title |
regeneration sample at T24, rep2 |
Sample type |
RNA |
|
|
Source name |
10-week-old normal female liver sample at 24 hours after 2/3 hepatectomy
|
Organism |
Mus musculus |
Characteristics |
Genotype: Female CD-1 mouse Age: 10 week
|
Treatment protocol |
After anesthesia with 100 mg/kg ketamine and 10 mg/kg Xylazine, the abdomen was prepped with alcohol and betadyne. Aftermidline laparotomy, the tip of the xiphoid was resected, and the liver exteriorized. A silk tie was placed around the three anterior lobes of the liver, including the gallbladder, and the 2/3 hepatectomy with cholecystectomy was completed. The liver was returned to the abdominal cavity and the abdomen closed in two layers. Postoperative analgesia consisted of Buprenorphine 0.05-0.1 mg/kg twice daily for 48 hours or until sacrifice. At harvest,mice were sacrificed with carbon dioxide asphyxiation followed by cervical dislocation.
|
Growth protocol |
All experiments used CD-1 mice obtained from Charles River Laboratories (Wilmington, MA) or our own breeding colony. Animals were maintained in a pathogenfree facility administered by Harvard Medical School in accordance with the institutional guidelines of Harvard Medical School and Beth Israel Deaconess Medical Center.
|
Extracted molecule |
total RNA |
Extraction protocol |
Trizol extraction of total RNA was performed according to the manufacturer's instructions.
|
Label |
biotin
|
Label protocol |
Biotinylated cRNA were prepared according to the standard Affymetrix protocol from 6 microg total RNA (Expression Analysis Technical Manual, 2001, Affymetrix).
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|
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Hybridization protocol |
Following fragmentation, 10 microg of cRNA were hybridized for 16 hr at 45C on Mouse Genome 2.0 Array. GeneChips were washed and stained in the Affymetrix Fluidics Station 400.
|
Scan protocol |
GeneChips were scanned using the Hewlett-Packard GeneArray Scanner G2500A.
|
Description |
Gene expression data from 10-week-old normal female liver sample.
|
Data processing |
The data were analyzed with dChip using smoothing spline invariant set method with the model based expression algorithm following the perfect match (PM)-mismatch (MM) difference model. In the dChip analysis, array outliers are not treated as missing expression values and no truncation on signal values is applied.
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|
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Submission date |
Feb 08, 2007 |
Last update date |
Aug 28, 2018 |
Contact name |
Hasan Huseyin Otu |
E-mail(s) |
[email protected]
|
Organization name |
Harvard Medical School
|
Department |
Medicine
|
Lab |
BIDMC Genomics Center
|
Street address |
4 Blackfan Circle Rm. 238
|
City |
Boston |
State/province |
MA |
ZIP/Postal code |
02115 |
Country |
USA |
|
|
Platform ID |
GPL1261 |
Series (1) |
GSE6998 |
Expression profiling of developmental and regenerating liver in mice |
|
Relations |
Reanalyzed by |
GSE119085 |