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Sample GSM2159724 Query DataSets for GSM2159724
Status Public on Aug 29, 2016
Title B1_Jurkat_THZ531_200nM_2
Sample type RNA
 
Source name Jurkat T-ALL
Organism Homo sapiens
Characteristics cell line: Jurkat
genotype: wildtype
treatment: Cells were treated with 200 nM THZ531 for 6 hours
Treatment protocol Jurkat cells were plated at 500,000 cells/ mL and incubated in media containing THZ531, THZ532, or THZ531R at the indicated concentrations or with DMSO for 6hrs. At the end of the experiment cells were collected by centrifugation and cell numbers were determined by manually counting cells using C-Chip disposable hemocytometers (Digital Bio, DHC-N01). 5,000,000 cells were isolated from each treatment condition.
Growth protocol Jurkat cells were grown in RPMI medium supplemented with 1% glutamine and 10% FBS. Cells were cultured at 37 degrees C in a humidified chamber in the presence of 5% CO2, unless otherwise noted.
Extracted molecule total RNA
Extraction protocol Total RNA from biological replicates (equivalent to 5 million cells per replicate) was subsequently isolated using RNeasy Plus Mini kit (Qiagen, cat#74134) following the manufacturer’s instructions and re-suspended in 50 μL nuclease-free water (Ambion, AM9938). Total RNA was spiked-in with ERCC RNA Spike-In Mix (Ambion, 4456740) and analyzed on Agilent 2100 Bioanalyzer for integrity.
Label biotin
Label protocol For microarray analysis, 100 ng of total RNA containing ERCC RNA Spike-In Mix (see above) was used to prepare biotinylated aRNA (cRNA) according to the manufacturer’s protocol (30 IVT Express Kit, Affymetrix 901228). Briefly, total RNA undergoes T7 oligo(dT)-primed reverse transcription to synthesize first-strand cDNA containing a T7 promoter sequence. This cDNA is then converted into a double-stranded DNA template for transcription using DNA Polymerase and RNase H to simultaneously degrade the RNA and synthesize second strand cDNA. In vitro transcription synthesizes aRNA and incorporates a biotin-conjugated nucleotide. The aRNA is then purified to remove unincorporated NTPs, salts, enzymes, and inorganic phosphate. Fragmentation of the biotin-labeled aRNA prepares the sample for hybridization onto GeneChip 3’ expression arrays.
 
Hybridization protocol Samples were prepared for hybridization using 10 µg of biotinylated aRNA in a 1X hybridization cocktail according the Affymetrix hybridization manual. Additional hybridization cocktail components were provided in the Affymetrix GeneChip Hybridization, Wash and Stain Kit. GeneChip arrays (Human PrimeView, Affymetrix 901837) were hybridized in a GeneChip Hybridization Oven at 45C for 16 hours at 60 RPM. Washing was done using a GeneChip Fluidics Station 450 according to the manufacturer’s instructions, using the buffers provided in the Affymetrix GeneChip Hybridization, Wash and Stain Kit.
Scan protocol Images were extracted with Affymetrix GeneChip Command Console (AGCC), and analyzed using GeneChip Expression Console. A Primeview CDF that included probe information for the ERCC controls (GPL16043), provided by Affymetrix, was used to generate .CEL files.
Data processing A CDF provided by Affymetrix, which contained the ERCC probes (PrimeView_withERCC_binary.cdf) was used instead of the standard PrimeView cdf. The data were analyzed with Bioconductor using the MAS5 normalization method. Then, these data were renormalized per batch (B1/B2) to the external spike-ins. See Loven, Orlando et al., Cell, 2012 for additional details.
 
Submission date May 18, 2016
Last update date Aug 29, 2016
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 GPL16043
Series (1)
GSE72022 Covalent targeting of remote cysteine residues to develop CDK12 and CDK13 inhibitors [Affymetrix]

Data table header descriptions
ID_REF
VALUE MAS 5.0 signal
B1_Jurkat_THZ531_200nM_2_renorm

Data table
ID_REF VALUE B1_Jurkat_THZ531_200nM_2_renorm
11715100_at 19.31762132 18.96975818
11715101_s_at 95.36649024 89.53244217
11715102_x_at 24.11886371 23.47723832
11715103_x_at 39.74377223 37.46916861
11715104_s_at 33.24642585 31.90268044
11715105_at 12.4373031 12.38225791
11715106_x_at 25.63467435 24.77908813
11715107_s_at 38.79199949 36.48602065
11715108_x_at 14.08040612 13.99612903
11715109_at 16.50149148 16.30575738
11715110_at 51.55457129 48.83194828
11715111_s_at 152.2858617 141.3207148
11715112_at 13.3231951 13.26010376
11715113_x_at 85.24952575 79.04282982
11715114_x_at 91.81556035 85.11716409
11715115_s_at 11.63359371 11.73393164
11715116_s_at 58.08609599 54.3982711
11715117_x_at 53.9881664 51.54726423
11715118_s_at 21.24035222 20.90174805
11715119_s_at 10.50877608 10.46533744

Total number of rows: 49494

Table truncated, full table size 1803 Kbytes.




Supplementary file Size Download File type/resource
GSM2159724_B1_Jurkat_THZ531_200nM_2.CEL.gz 1.8 Mb (ftp)(http) CEL
Processed data included within Sample table

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