NCBI Logo
GEO Logo
   NCBI > GEO > Accession DisplayHelp Not logged in | LoginHelp
GEO help: Mouse over screen elements for information.
          Go
Sample GSM175290 Query DataSets for GSM175290
Status Public on May 02, 2007
Title AR2-MB-24-1-604
Sample type RNA
 
Channel 1
Source name midbrain (control)
Organism Mus musculus
Characteristics Mid Brain from male DBA/1 mice 31 d after i.d. injection of Complete Freunds adjuvant
Treatment protocol Eight week old DBA/1 male mice were injected i.d. with 200 ul of Complete Freunds ajuvant at day 24 were injected with LPS and sacrifice by decapitation at day 31 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 (collagen)
Organism Mus musculus
Characteristics Mid Brain from male DBA/1 mice 31 d after i.d. injection of Type II collagen in Complete Freunds adjuvant
Treatment protocol Eight week old DBA/1 male mice were injected i.d. with 100 ul type II Collagen in 100 ul of Complete Freunds ajuvant at day 24 were injected with LPS and sacrifice by decapitation at day 31 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 male DBA/1 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 GPL4987
Series (2)
GSE7284 profiling of midbrain from arthritic DBA/1 mice vs. control DBA/1 mice
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 218191 100204 318593 96596 164 0.1251
2 159062 69462 0 0 102 0.1440
3 97705 39501 0 0 57 0.2234
4 139376 51408 0 0 108 0.1095
5 129902 48984 175993 44720 104 0.1846
6 0.820599980175554 125517 51566 109291 42716 118 0.1687
7 0.90530060056262 71323 35446 55372 24050 74 0.2499
8 140446 55151 115684 43754 131 0.0986
9 79769 34760 0 0 79 0.0647
10 118037 39120 93193 28960 80 0.1561
11 130880 51339 103488 36842 109 0.1064
12 0.833967056783325 117539 53448 125256 39678 102 0.1962
13 62395 28600 0 0 50 0.0934
14 111410 53106 67870 39114 106 0.0912
15 0 0 0 0 24 0.0000
16 109318 47045 0 0 97 0.0954
17 174735 79119 0 0 149 0.0550
18 72193 29097 0 0 53 0.1626
19 196705 76160 157968 51136 136 0.3747
20 235934 84270 209624 58989 159 0.4043

Total number of rows: 10080

Table truncated, full table size 449 Kbytes.




Supplementary file Size Download File type/resource
GSM175290-1.txt.gz 359.6 Kb (ftp)(http) TXT
GSM175290-2.txt.gz 366.2 Kb (ftp)(http) TXT
GSM175290-3.txt.gz 369.7 Kb (ftp)(http) TXT

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