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Sample GSM298271 Query DataSets for GSM298271
Status Public on Jun 18, 2008
Title E11.5_heterozygous_embryo#10
Sample type RNA
 
Source name Ott1 knockdown, heterozygous embryo #10
Organism Mus musculus
Characteristics The mouse ES cell line XK135 (obtained from BayGenomics; funded by the National Heart, Lung, and Blood Institute, http://baygenomics.ucsf.edu), harbours a LacZ-neo fusion cassette inserted into the first coding exon of Ott1, 20 nt upstream the initiator codon, generating a low-expression Ott1XK135 allele. After injection into C57BL/6 blastocysts, the chimeric mice were bred for germline transmission. Genomic DNA from tail snips or yolk sacs was used for PCR genotyping. Ott1 alleles were detected by using primers, which span the XK135 insertion site.
Treatment protocol Dissected embryos, snap-frozen in liquid nitrogen
Extracted molecule total RNA
Extraction protocol Total RNA was extracted and purified using RiboPure RNA isolation (Ambion).
Total RNA samples were quantitated by UV spectrophotometry (OD260/280).
Quality of Total RNA was assessed using an Agilent Bioanalyzer.
Label biotin
Label protocol First and second strand cDNA was prepared from the total RNA samples using standard CodeLink protocol.
Biotinylated cRNA target was prepared from the DNA template and verified on the Bioanalyzer.
cRNA was fragmented to uniform size and verified on the Bioanalyzer.
 
Hybridization protocol CodeLink Bioarrays were hybridized with the cRNA target and stained with Cy5-streptavidin.
Scan protocol Slides were washed and then scanned on an Axon GenePix 4000B scanner.
Description Mice harboring a low expression Ott1 allele were mated and embryos at day E11.5 were dissected and genotyped.
Data processing Data were analyzed for quality with CodeLink software package, and transcripts of which the values were missing in at least one mictoarray were removed from the dataset, and raw intensity values less than 0.01 were set to 0.01.

Normalization Method: Median-Normalization;
Computation Method for Median: Spot Based;
Threshold Trim Percentage: 20;
Raw TrimMean Negative Control: 14.47337532;
Normalized TrimMean Negative Control: 0.297574033;
Median: 48.63789749
 
Submission date Jun 13, 2008
Last update date Jun 17, 2008
Contact name Andrei S Zolotukhin
E-mail(s) zolotukh@ncifcrf.gov
Organization name NCI-Frederick
Street address P.O. Box B
City Frederick
State/province MD
ZIP/Postal code 21702
Country USA
 
Platform ID GPL2897
Series (1)
GSE11785 Control of gene expression by Ott1/RBM15 protein

Data table header descriptions
ID_REF
VALUE Median-normalized intensity
SIGNAL_RAW Raw intensity

Data table
ID_REF VALUE SIGNAL_RAW
1002 16.79167049 816.7115479
1003 0.161344513 7.847457886
1004 0.921556661 44.82257843
1005 0.995648124 48.42623138
1006 0.085277699 4.147727966
1010 2.096089194 101.9493713
1012 0.546096264 26.56097412
1013 0.365636343 17.78378296
1017 -0.03889081 -1.89156723
1018 0.523175405 25.44615173
1019 0.283402299 13.78409195
1020 0.181412617 8.82352829
1024 0.161191181 7.840000153
1026 1.631724155 79.3636322
1027 0.252805284 12.29591751
1030 0.6381855 31.04000092
1031 0.04820985 2.344825745
1034 0.603817701 29.36842346
1039 0.876088744 42.6111145
1040 0.215587398 10.48571777

Total number of rows: 35587

Table truncated, full table size 1049 Kbytes.




Supplementary file Size Download File type/resource
GSM298271.txt.gz 1.4 Mb (ftp)(http) TXT
Processed data included within Sample table

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