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Sample GSM358854 Query DataSets for GSM358854
Status Public on Jan 31, 2009
Title rAAVpp65mIINLSKO-rep2
Sample type RNA
 
Source name fibroblasts-MRC-5 cells transduced with recombinant DNA, mutated PP65
Organism Homo sapiens
Characteristics mutated PP65
Treatment protocol The MRC-5 cells were transduced in triplicate, with rAAVintA, rAAVpp65N, rAAVpp65NLSKO and incubated for 48hrs at 37C.
Growth protocol The MRC-5 cells were grown in Dulbecco’s modified Eagle’s medium with low glucose (DMEM low) supplemented with 10% fetal bovine serum ( FBS) ( Hyclone, Utah), 2mM L-glutamine(G ), 100units/ml penicillin and 100μg/ml streptomycin ( P/S)
Extracted molecule total RNA
Extraction protocol Total RNA was purified with RNeasy kit (Qiagen, Valencia, CA) according to the manufacturer’s instructions. ). After ribosomal RNA reduction (Invitrogen, Carlsbad, CA) to remove most of the 18S and 28S rRNAs, the GeneChip WT (whole transcript) cDNA Synthesis Kit, WT cDNA Amplification Kit, and WT Terminal Labeling Kit (Affymetrix, Inc., Santa Clara, CA) were used for target preparation. Ten µg of cRNA (antisense RNA) were added to the second-cycle cDNA reaction followed by fragmentation and Terminal Labeling process.
Label Biotin
Label protocol One µg of each sample was processed using the Affymetrix GeneChip Whole Transcript Sense Target Labeling Assay (https://www.affymetrix.com/support/downloads/manuals/wt_sensetarget_label_manual.pdf
 
Hybridization protocol The hybridization cocktails containing 2.5 ug of the fragmented, end-labeled cDNA were applied to the GeneChip® Human Gene 1.0 ST arrays. Hybridization was performed for 16 hours, and the arrays were washed and stained with the GeneChip Fluidics Station 450 using FS450_0007 script.
Scan protocol Arrays were scanned using the Affymetrix GCS 3000 7G and GeneChip Operating Software v. 1.4 to produce CEL intensity files.
Description MRC-5 cells transduced with rAAV mutated CMV PP65
Data processing Data were background corrected with GC bin, quantile normalized and summarized by interPLIER algorithm with Affymetrix Expression Console.
 
Submission date Jan 08, 2009
Last update date Jan 09, 2009
Contact name Xiwei Wu
E-mail(s) xwu@coh.org
Organization name City of Hope National Medical Center
Department Computational and Quantitative Medicine
Street address 1500 E. Duarte Rd.
City Duarte
State/province CA
ZIP/Postal code 91010
Country USA
 
Platform ID GPL6244
Series (1)
GSE14347 Knock-out of the nuclear localization in pp65 protein of Cytomegalovirus: biologic and immunologic effects

Data table header descriptions
ID_REF
VALUE Expression Console processed intensity at linear scale

Data table
ID_REF VALUE
7896736 28.86155
7896738 29.98355
7896740 14.68304
7896746 130.6981
7896748 309.4175
7896750 35.55111
7896752 1076.806
7896754 53.59571
7896756 108.9023
7896759 58.08476
7896761 741.5876
7896779 598.6157
7896798 999.0889
7896817 1013.73
7896822 1435.12
7896859 186.7825
7896861 5.573188
7896863 218.6846
7896865 475.9774
7896878 705.7544

Total number of rows: 33297

Table truncated, full table size 550 Kbytes.




Supplementary file Size Download File type/resource
GSM358854.CEL.gz 4.3 Mb (ftp)(http) CEL
Processed data included within Sample table

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