NCBI Logo
GEO Logo
   NCBI > GEO > Accession DisplayHelp Not logged in | LoginHelp
GEO help: Mouse over screen elements for information.
          Go
Sample GSM175426 Query DataSets for GSM175426
Status Public on May 02, 2007
Title M-MB-18-5-535
Sample type RNA
 
Channel 1
Source name midbrain (control)
Organism Mus musculus
Characteristics Mid Brain from female Balb/c mice 18 h after s.c. injection of PBS
Treatment protocol Eight week old Balb/c female mice were injected s.c. with 100 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
 
Channel 2
Source name midbrain (18 h after injection of 4T-1 mammary cancer cells)
Organism Mus musculus
Characteristics Mid Brain from female Balb/c mice 18 h after s.c. injection of 4T-1 mammary cancer cells
Treatment protocol Eight week old Balb/c female mice were injected s.c. with 1E5 4T-1 cells in 100 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 Mid Brain of female balb/c mice
Data processing Data was log2 transformed and normalizaed with an intensity- and location-dependent loess fit
 
Submission date Mar 14, 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)
GSE7298 profiling of midbrain from mice s.c. injected with 4T-1 mammary carcinoma cells vs. PBS
GSE7565 Profiling brain and liver tissues from mice

Data table header descriptions
ID_REF
VALUE normalized log2 ratios CH2 / CH1
CH1_MEAN Channel 1 mean intensity
CH1_BG Channel 1 mean background intensity
CH2_MEAN Channel 2 mean intensity
CH2_BG Channel 2 mean background intensity
AREA Spot total area in pixels
SF Percentage of nonsaturated pixels

Data table
ID_REF VALUE CH1_MEAN CH1_BG CH2_MEAN CH2_BG AREA SF
1 0 0 0 0 63 0.0000
2 0.0432869618228313 53239 20160 0 0 60 0.0843
3 0 0 0 0 101 0.0000
4 19917 6402 17960 3762 22 0.1735
5 54829 21608 58088 10877 73 0.0658
6 0 0 0 0 44 0.0000
7 0 0 0 0 22 0.0000
8 64133 23937 0 0 79 0.0883
9 -0.0224632865673606 51076 18476 54428 9424 62 0.0862
10 0 0 123955 15006 82 0.1450
11 0.0442132927632433 89441 37296 179173 19376 112 0.2982
12 -0.161794396120058 43155 18468 44987 9291 57 0.0830
13 0 0 0 0 60 0.0000
14 -0.124448159295738 110520 39600 103699 18720 120 0.1423
15 65607 29890 0 0 70 0.0660
16 0 0 0 0 52 0.0000
17 -0.0377152764736664 169454 75840 345548 37288 158 0.1071
18 -0.239264173340423 0 0 0 0 62 0.0000
19 0 0 0 0 149 0.0000
20 102290 44233 0 0 89 0.0570

Total number of rows: 10080

Table truncated, full table size 414 Kbytes.




Supplementary file Size Download File type/resource
GSM175426-1.txt.gz 316.0 Kb (ftp)(http) TXT
GSM175426-2.txt.gz 322.2 Kb (ftp)(http) TXT
GSM175426-3.txt.gz 324.9 Kb (ftp)(http) TXT

| NLM | NIH | GEO Help | Disclaimer | Accessibility |
NCBI Home NCBI Search NCBI SiteMap