|
Status |
Public on Aug 31, 2009 |
Title |
mouse48_vs_mixed_sex_pool: muscle |
Sample type |
RNA |
|
|
Channel 1 |
Source name |
mouse48, muscle
|
Organism |
Mus musculus |
Characteristics |
strain: CAST/EiJ x C57BL/6J treatment category: test sample tissue: muscle sex: female
|
Treatment protocol |
Mice were fasted overnight before they were killed. Their tissues were collected, flash frozen in liquid nitrogen, and stored in −80 °C prior to RNA isolation. All procedures of housing and treatment of animals were performed in accordance with Institutional Animal Care and Use Committee regulations.
|
Growth protocol |
All mice were maintained on a 12 h light–12 h dark cycle and fed ad libitum. Mice were fed Purina Chow until 10 wk of age, and then fed western diet (Teklad 88137, Harlan Teklad) for the subsequent 8 wk.
|
Extracted molecule |
polyA RNA |
Extraction protocol |
Mouse tissues were homogenized, and total RNA extracted using Trizol reagent (Invitrogen) according to manufacturer's protocol.
|
Label |
Cy5
|
Label protocol |
Three micrograms of total RNA was reverse transcribed and labeled with either Cy3 or Cy5 fluorochrome. Labeled complementary RNA (cRNA) from each F2 animal was hybridized against a cross-specific pool of labeled cRNAs constructed from equal aliquots of RNA from 150 F2 animals and parental mouse strains for each of the three tissues.
|
|
|
Channel 2 |
Source name |
reference pool (mixed sex, muscle)
|
Organism |
Mus musculus |
Characteristics |
strain: CAST/EiJ x C57BL/6J treatment category: reference pool tissue: muscle sex: mixed
|
Treatment protocol |
Mice were fasted overnight before they were killed. Their tissues were collected, flash frozen in liquid nitrogen, and stored in −80 °C prior to RNA isolation. All procedures of housing and treatment of animals were performed in accordance with Institutional Animal Care and Use Committee regulations.
|
Growth protocol |
All mice were maintained on a 12 h light–12 h dark cycle and fed ad libitum. Mice were fed Purina Chow until 10 wk of age, and then fed western diet (Teklad 88137, Harlan Teklad) for the subsequent 8 wk.
|
Extracted molecule |
polyA RNA |
Extraction protocol |
Mouse tissues were homogenized, and total RNA extracted using Trizol reagent (Invitrogen) according to manufacturer's protocol.
|
Label |
Cy3
|
Label protocol |
Three micrograms of total RNA was reverse transcribed and labeled with either Cy3 or Cy5 fluorochrome. Labeled complementary RNA (cRNA) from each F2 animal was hybridized against a cross-specific pool of labeled cRNAs constructed from equal aliquots of RNA from 150 F2 animals and parental mouse strains for each of the three tissues.
|
|
|
|
Hybridization protocol |
The hybridizations were performed to single arrays (individuals F2 samples labeled with Cy5 and reference pools labeled with Cy3 fluorochromes) for 24 h in a hybridization chamber, washed, and scanned using a confocal laser scanner. Arrays were quantified on the basis of spot intensity relative to background, adjusted for experimental variation between arrays using average intensity over multiple channels, and fitted to a previously described error model to determine significance21 (type I error)
|
Scan protocol |
Standard dual-channel Agilent scanner with manufacturer provided software.
|
Description |
ID278
|
Data processing |
See Rosetta Error Model (PMID: 16522673)
|
|
|
Submission date |
May 26, 2009 |
Last update date |
May 29, 2009 |
Contact name |
Tomas Babak |
E-mail(s) |
tomas_babak@merck.com, tomas.babak@utoronto.ca
|
Phone |
416-978-1839
|
Fax |
416-978-8528
|
Organization name |
Best Institute
|
Department |
Banting and Best Department of Medical Research
|
Lab |
Timothy Hughes
|
Street address |
112 College St
|
City |
Toronto |
State/province |
ON |
ZIP/Postal code |
M5G1L6 |
Country |
Canada |
|
|
Platform ID |
GPL8591 |
Series (1) |
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