NCBI Logo
GEO Logo
   NCBI > GEO > Accession DisplayHelp Not logged in | LoginHelp
GEO help: Mouse over screen elements for information.
          Go
Sample GSM3966997 Query DataSets for GSM3966997
Status Public on Apr 15, 2020
Title SuvER-4146 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 GSM3928718

Data table header descriptions
ID_REF
VALUE normalized log2 signal intensity

Data table
ID_REF VALUE
1415670_at 8.573723701
1415671_at 9.053096848
1415672_at 10.47072461
1415673_at 9.448890267
1415674_a_at 8.884382197
1415675_at 8.425151409
1415676_a_at 10.46558306
1415677_at 7.422400208
1415678_at 9.179800634
1415679_at 10.08137181
1415680_at 9.457277512
1415681_at 9.663273451
1415682_at 7.946223334
1415683_at 10.17754441
1415684_at 7.537018062
1415685_at 9.155571388
1415686_at 8.171922732
1415687_a_at 10.3973656
1415688_at 9.27759308
1415689_s_at 7.751871843

Total number of rows: 45101

Table truncated, full table size 1026 Kbytes.




Supplementary file Size Download File type/resource
GSM3966997_4146_UT.CEL.gz 3.5 Mb (ftp)(http) CEL
Processed data included within Sample table

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