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Status |
Public on May 02, 2007 |
Title |
P-CO-18-4-437 |
Sample type |
RNA |
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Channel 1 |
Source name |
prefrontal cortex (control)
|
Organism |
Mus musculus |
Characteristics |
Pre-frontal cortex from male C57Bl/6 mice 18 h after s.c. injection of PBS
|
Treatment protocol |
Eight week old C57Bl/6 male mice were injected s.c. with 300 ul PBS and sacrifice by decapitation after 18 h
|
Growth protocol |
Mice were housed in HEPA filtered air racks (Tecniplast, Italy) with food and water ad libitum
|
Extracted molecule |
total RNA |
Extraction protocol |
Total RNA was extracted using TRIzol Reagent (Invitrogen)
|
Label |
Cy3
|
Label protocol |
RNA was reversed transcribed using Superscript II RT (Invitrogen) with oligo dT primers and random primers, both in the presence of aa-dUTP (Sigma). The cDNA was labeled with Cy3 or Cy5 dyes (Amersham), resuspended in DMSO, and incubated for 1 hr at room temperature in the dark. The probes were purified using the SNAP Gel Purification Kit (Invitrogen) following manufacturer instructions with the following modification: at the initial step, 500 ul of loading buffer (2.25 M guanidinium HCl in 70% isopropanol) were added to the sample, placed in a SNAP column and incubated for 4 min before the first centrifugation
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Channel 2 |
Source name |
prefrontal cortex (18 h after injection of LL/2(LLC1) lung tumor cells)
|
Organism |
Mus musculus |
Characteristics |
Pre-frontal cortex form male C57Bl/6 mice 18 h after s.c. injection of LL/2(LLC1) lung cancer cell
|
Treatment protocol |
Eight week old C57Bl/6 male mice were injected s.c. with 1E6 LL/2(LLC1) lung tumor cells in 300 ul PBS and sacrifice by decapitation after 18 h
|
Growth protocol |
Mice were housed in HEPA filtered air racks (Tecniplast, Italy) with food and water ad libitum
|
Extracted molecule |
total RNA |
Extraction protocol |
Total RNA was extracted using TRIzol Reagent (Invitrogen)
|
Label |
Cy5
|
Label protocol |
RNA was reversed transcribed using Superscript II RT (Invitrogen) with oligo dT primers and random primers, both in the presence of aa-dUTP (Sigma). The cDNA was labeled with Cy3 or Cy5 dyes (Amersham), resuspended in DMSO, and incubated for 1 hr at room temperature in the dark. The probes were purified using the SNAP Gel Purification Kit (Invitrogen) following manufacturer instructions with the following modification: at the initial step, 500 ul of loading buffer (2.25 M guanidinium HCl in 70% isopropanol) were added to the sample, placed in a SNAP column and incubated for 4 min before the first centrifugation
|
|
|
|
Hybridization protocol |
Slides were prehybridised at 42°C in 2X SSC, 0.1% SDS, 1% BSA. Labeled probes were mixed with hybridization buffer containing 30% formamide and hybridized overnight at 42°C
|
Scan protocol |
Images were obtained with a VersArray ChipReader system (BioRad) at 10 um resolution and 16bit depth. Each slide was scanned three times, each time with a 5% increment in the sensitivity of the scanner. The data integration for multipole scanning were calculated by M = log2(cy3 / cy2) and A = 0.5 * log2(cy2 * cy3) values for all the possible combinations between channels among the three scannings. Quality score for each couple of channels was calculated as QS = min(QScy2, QScy3). The resulting 9 sets of A and M values were averaged using the QS as weights to obtain the integrated A and M sets.
|
Description |
Pre-frontal cortex of male c57Bl/6 mice
|
Data processing |
Data was log2 transformed and normalizaed with an intensity- and location-dependent loess fit
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|
Submission date |
Mar 13, 2007 |
Last update date |
May 04, 2007 |
Contact name |
Mariano Cesar Salibe |
E-mail(s) |
msalibe@leloir.org.ar
|
Organization name |
Gentron LLC
|
Street address |
Av. Patricias Argentinas 435
|
City |
Ciudad de Buenos Aires |
ZIP/Postal code |
1425 |
Country |
Argentina |
|
|
Platform ID |
GPL4986 |
Series (2) |
GSE7300 |
profiling of prefrontal cortex from mice s.c. injected with LL/2(LLC1) lung carcinoma cells vs. PBS |
GSE7565 |
Profiling brain and liver tissues from mice |
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