NCBI Logo
GEO Logo
   NCBI > GEO > Accession DisplayHelp Not logged in | LoginHelp
GEO help: Mouse over screen elements for information.
          Go
Sample GSM722136 Query DataSets for GSM722136
Status Public on Aug 16, 2012
Title TAL1_shRNA1_Jurkat, biological replicate1
Sample type RNA
 
Source name Jurkat cells transduced with TAL1 shRNA1 for 72 hrs
Organism Homo sapiens
Characteristics cell line: Jurkat E6-1
Treatment protocol The Jurkat cells were infected with shRNA lentivirus in the presence of polybrene by centrifugation at 2,500 rpm for 1.5 h followed by a incubation for overnight in a CO2 incubator. Total RNA was harvested after 3 days of infection.
Growth protocol The Jurkat T-ALL cell line was grown in RPMI-1640 medium supplemented with 10% FBS, L-glutamine and penicillin/streptomycin at 37C in a CO2 incubator.
Extracted molecule total RNA
Extraction protocol Total RNA was extracted using Trizol (Invitrogen) followed by a column purification using RNeasy Mini Kit (QIAGEN, Valencia, CA) according to the manufacturers instructions.
Label biotin
Label protocol Biotinylated cRNA were prepared according to the standard Affymetrix protocol from 1 ug total RNA (Expression Analysis Technical Manual, 2001, Affymetrix).
 
Hybridization protocol Following fragmentation, 10 ug of cRNA were hybridized for 16 hr at 45C on GeneChip Human Genome Array. GeneChips were washed and stained in the Affymetrix Fluidics Station 400.
Scan protocol GeneChips were scanned using the Hewlett-Packard GeneArray Scanner G2500A.
Description Gene expression data from Jurkat cells transduced with TAL1 shRNA1 for 72 hrs
Data processing Individual Arrays were normalized using Robust Multichip Averaging (RMA) within the Affytmetrix package from Bioconductor. Probeset definitions for RefSeq genes were derived from CDF version 13.0.0 downloaded from (http://brainarray.mbni.med.umich.edu/Brainarray/Database/CustomCDF/genomic_curated_CDF.asp) based on improved definitions (Sandberg and Larsson, 2007).
 
Submission date May 10, 2011
Last update date Aug 16, 2012
Contact name Richard A Young
E-mail(s) young_computation@wi.mit.edu
Phone 617-258-5219
Organization name Whitehead Institute for Biomedical Research
Lab Young Lab
Street address 9 Cambridge Center
City Cambridge
State/province MA
ZIP/Postal code 02142
Country USA
 
Platform ID GPL13232
Series (2)
GSE29179 Identification of differentially expressed genes upon shRNA knockdown of TAL1 and its regulatory partners in T-ALL cells (Jurkat)
GSE29181 Core transcriptional regulatory circuit controlled by the TAL1 complex in human T-cell acute lymphoblastic leukemia

Data table header descriptions
ID_REF
VALUE RMA normalized log base 2 signal intensity

Data table
ID_REF VALUE
NM_000014_at 3.22
NM_000015_at 4.03
NM_000016_at 11.74
NM_000017_at 7.61
NM_000018_at 10.17
NM_000019_at 10.21
NM_000020_at 4.72
NM_000021_at 6.31
NM_000022_at 13.64
NM_000023_at 3.68
NM_000024_at 4.13
NM_000025_at 4.93
NM_000026_at 12.07
NM_000027_at 7.41
NM_000028_at 10.55
NM_000029_at 4.84
NM_000030_at 4.82
NM_000031_at 7.13
NM_000032_at 4.70
NM_000033_at 6.41

Total number of rows: 30927

Table truncated, full table size 573 Kbytes.




Supplementary file Size Download File type/resource
GSM722136_TS_7.CEL.gz 4.9 Mb (ftp)(http) CEL
Processed data included within Sample table

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