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Sample GSM283118 Query DataSets for GSM283118
Status Public on Apr 22, 2008
Title Dicer1-null 27H10 versus wild-type ES cells 2
Sample type RNA
 
Channel 1
Source name DicerNull27 h10
Organism Mus musculus
Characteristics Dicer-1 null 27H10 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 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 wtEstCells
Organism Mus musculus
Characteristics ES wild type cell line
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 Null27h10 / wt
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 -0.0062 0.9957086
117 -1.6230 0.32466397
1414 -1.5093 0.35129255
1465 1.3491 2.5475478
1315 1.2538 2.3846307
836 0.0027 1.001853
1401 -3.0436 0.12127677
141 -1.6962 0.30859196
3027 1.0376 2.0528066
1638 2.8606 7.263194
758 0.6301 1.5476847
2290 -0.0287 0.9802697
1644 0.0043 1.0029929
7021 -0.0055 0.9962015
20775 -0.1602 0.89493054
11388 0.8930 1.8569709
16634 -0.0946 0.9365101
9411 -0.2840 0.8212917
8322 0.0335 1.0234908
26137 -0.6195 0.6509169

Total number of rows: 41263

Table truncated, full table size 946 Kbytes.




Supplementary file Size Download File type/resource
GSM283118.txt.gz 14.2 Mb (ftp)(http) TXT
Processed data included within Sample table

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