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Sample GSM3967000 Query DataSets for GSM3967000
Status Public on Apr 15, 2020
Title SuvER-4936 native
Sample type RNA
 
Source name primary lymphoma cells, isolated from lymph nodes of Emu-myc transgenic mice with palpable lymphadenopathy
Organism Mus musculus
Characteristics cell type: primary lymphoma cells
treatment: native
genotype: Suv39h1- plus Suv39h1ER
phenotype: non-senescent
Treatment protocol Freshly isolated lymphoma cells were retrovirally transduced by Bcl2 (MSCVpuro) and selected with Puromycin for 48h. These Myc;Bcl2 cells were either left untreated or treated in vitro with 0.05µg/ml Adriamycin for 5 days
Growth protocol Primary Emu-myc lymphoma cells were cultivated in B-cell medium (DMEM and IMDM in 1:1 ratio, 10%FBS, 4mM L-glutamine, 25µM beta-mercaptoethanol, 100U/ml penicilin/streptamycin) on gamma-irradiated (20Gy) NIH 3T3 cells as feeder.
Extracted molecule total RNA
Extraction protocol The total RNA from untreated or 5 days ADR treated Myc;Bcl2 lymphomas was prepared using an RNeasy Mini kit (QIAGEN, Valencia, California) according to the manufacturer's instruction.
Label biotin
Label protocol Biotinylated cRNA was prepared according to the standard Affymetrix protocol (One Cycle Target labeling protocol) from 3 ug total RNA.
 
Hybridization protocol Following fragmentation, 10 ug of cRNA were hybridized for 16 hr at 45°C on MOE430 2.0 Arrays (Affymetrix). GeneChips were washed and stained with standard protocols in the Affymetrix Fluidics Station 450.
Scan protocol GeneChips were scanned using the Scanner G3000
Description Primary lymphoma cells, isolated from lymph nodes of Emu-myc transgenic mice and retrovirally transduced by Bcl2 overexpression
Data processing Affymetrix CEL files were imported into R (version 3.5.0) and processed by the RMA workflow implemented in the oligo package (median polish probe set summarization, RMA background correction, quantile normalization). Batch Effects were reduced by Empirical Bayes methods (ComBat) in the sva package. Treatment and phenotype were included as covariates in batch correction.
 
Submission date Jul 23, 2019
Last update date Apr 15, 2020
Contact name Maja Milanovic
E-mail(s) maja.milanovic@charite.de
Organization name Charite University Medicine, Berlin
Department Hematology and Oncology
Lab Clemens Schmitt
Street address Augustenburgerplatz 1
City Berlin
ZIP/Postal code 13353
Country Germany
 
Platform ID GPL1261
Series (1)
GSE134753 Expression data from treatment-induced senescence in mouse Emu-myc B-cell lymphoma model.
Relations
Reanalysis of GSM3928724

Data table header descriptions
ID_REF
VALUE normalized log2 signal intensity

Data table
ID_REF VALUE
1415670_at 8.292544035
1415671_at 8.888089055
1415672_at 10.439941
1415673_at 8.825355446
1415674_a_at 8.59690127
1415675_at 7.335774486
1415676_a_at 9.701699586
1415677_at 7.652269095
1415678_at 9.123286535
1415679_at 10.54544612
1415680_at 9.666427462
1415681_at 8.741771161
1415682_at 7.974093626
1415683_at 10.37729355
1415684_at 7.698353979
1415685_at 8.747666466
1415686_at 7.96969234
1415687_a_at 11.32434685
1415688_at 9.26415682
1415689_s_at 7.676415903

Total number of rows: 45101

Table truncated, full table size 1026 Kbytes.




Supplementary file Size Download File type/resource
GSM3967000_4936_ut.CEL.gz 3.4 Mb (ftp)(http) CEL
Processed data included within Sample table

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