NCBI Logo
GEO Logo
   NCBI > GEO > Accession DisplayHelp Not logged in | LoginHelp
GEO help: Mouse over screen elements for information.
          Go
Sample GSM283108 Query DataSets for GSM283108
Status Public on Apr 22, 2008
Title Dicer1-null 27G5 cells overexpressing Dnmt1 versus Dicer1-null 27G5 cells 2
Sample type RNA
 
Channel 1
Source name 27 g5+DNMT1
Organism Mus musculus
Characteristics Dicer1-null 27G5 cells overexpressing Dnmt1
Treatment protocol No special treatment were applied, cells were growth in appropriate conditions (see growth protocol) and harvested to prepare RNA.
Growth protocol Cell lines wild type and Dicer-1 (cultures 27G5 and 27H10) or Dicer-1 null (27G5 or 27H10) + DNMT1 and Dicer-1 null (27G5 and 27H10) + DNMT3a3b, were cultivated on gelatin-coated plates with media supplemented with Leukemia Inhibitory Factor.
Extracted molecule total RNA
Extraction protocol Commercial RNeasy kit (Qiagen) was used in spin-column format by following manufacturer instructions. Total RNA was analysed by Lab-chip technology on an Agilent 2100 Bioanalyzer. Samples' RNA Integrity Numbers were in the range 8.0 to 9.5
Label Cy3
Label protocol Amount of nucleic acid labeled: 2ug.Amplification: by RNA polymerases.Commercial "Two-Color Microarray-Based Gene Expression Analysis" kit by following manufacturer instructions. Agilent manual G4140-90050 Ver. 5.5 Feb 2007. Briefly, MMLV-RT retrotranscription of sample from a T7 promoter primer is followed by a T7 RNA pol catalysed in vitro transcription reaction in the presence of either Cy3-CTP or Cy5-CTP fluorophores. Labeled samples are purified with silica-based RNeasy spin columns (Qiagen).
 
Channel 2
Source name Dicer Null 27G5
Organism Mus musculus
Characteristics Dicer-1 null 27G5 cells
Treatment protocol No special treatment were applied, cells were growth in appropriate conditions (see growth protocol) and harvested to prepare RNA.
Growth protocol Cell lines wild type and Dicer-1 (cultures 27G5 and 27H10) or Dicer-1 null (27G5 or 27H10) + DNMT1 and Dicer-1 null (27G5 and 27H10) + DNMT3a3b, were cultivated on gelatin-coated plates with media supplemented with Leukemia Inhibitory Factor.
Extracted molecule total RNA
Extraction protocol Commercial RNeasy kit (Qiagen) was used in spin-column format by following manufacturer instructions. Total RNA was analysed by Lab-chip technology on an Agilent 2100 Bioanalyzer. Samples' RNA Integrity Numbers were in the range 8.0 to 9.5
Label Cy5
Label protocol Amount of nucleic acid labeled: 2ug.Amplification: by RNA polymerases.Commercial "Two-Color Microarray-Based Gene Expression Analysis" kit by following manufacturer instructions. Agilent manual G4140-90050 Ver. 5.5 Feb 2007. Briefly, MMLV-RT retrotranscription of sample from a T7 promoter primer is followed by a T7 RNA pol catalysed in vitro transcription reaction in the presence of either Cy3-CTP or Cy5-CTP fluorophores. Labeled samples are purified with silica-based RNeasy spin columns (Qiagen).
 
 
Hybridization protocol Chamber type: SureHyb hybridization chamber (Agilent). Quantity of labeled extract used: 825 ng. Duration: 17 hours.Volume: 100 uL.Temperature (ÂșC): 65.
Scan protocol Scanned on an G2565BA DNA microarray scanner (Agilent). Images were quantified using Agilent Feature Extraction Software (ver. 9.5.1).
Description no additional information
Dye swap technical replicate of MT1 / Null27g5
Data processing Per Spot: Divide by control channel. Each gene's measured intensity was divided by its control channel value in each sample; if the control channel was below 0 then 0 was used instead. If the control channel and the signal channel were both below 0 then no data was reported.
Per Chip: Normalize to 50th percentile. Each measurement was divided by the 50,0th percentile of all measurements in that sample.The percentile was calculated using only genes marked present.
 
Submission date Apr 21, 2008
Last update date Apr 22, 2008
Contact name Roberta Benetti
E-mail(s) roberta.benetti@lncib.it
Organization name CNIO
Street address Calle Melchor Fernandez Almagro
City Madrid
ZIP/Postal code 28003
Country Spain
 
Platform ID GPL4134
Series (1)
GSE11229 Dicer-null cell lines vs. wt ES cells and Dicer-null cell lines vs. Dicer-null cells overexpressing Dnmt1 or Dnmt3a/3b

Data table header descriptions
ID_REF
VALUE log2 of PRE_VALUE
PRE_VALUE normalized ratio representing test/reference

Data table
ID_REF VALUE PRE_VALUE
1475 0.1264 1.0915923
117 -1.4371 0.36930612
1414 -1.2455 0.4217536
1465 1.5671 2.9629872
1315 1.5460 2.9200208
836 0.1682 1.1236247
1401 -2.7329 0.1504208
141 -1.4376 0.36918908
3027 1.3370 2.5261784
1638 3.0834 8.476284
758 0.1396 1.1015675
2290 0.2844 1.217926
1644 0.3672 1.2898045
7021 0.2077 1.1548597
20775 0.2798 1.2140001
11388 -0.2687 0.8300479
16634 -0.5865 0.66593736
9411 0.0277 1.0193856
8322 0.0006 1.0003976
26137 -0.7504 0.59442586

Total number of rows: 41263

Table truncated, full table size 935 Kbytes.




Supplementary file Size Download File type/resource
GSM283108.txt.gz 15.4 Mb (ftp)(http) TXT
Processed data included within Sample table

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