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Sample GSM3966993 Query DataSets for GSM3966993
Status Public on Apr 15, 2020
Title 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-
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 GSM1083878

Data table header descriptions
ID_REF
VALUE normalized log2 signal intensity

Data table
ID_REF VALUE
1415670_at 8.257046499
1415671_at 8.333293461
1415672_at 10.62240615
1415673_at 8.70414144
1415674_a_at 8.389654532
1415675_at 8.205437017
1415676_a_at 10.05164541
1415677_at 6.82677474
1415678_at 9.92564528
1415679_at 10.00284113
1415680_at 9.248886271
1415681_at 9.566173421
1415682_at 7.475414909
1415683_at 9.830761529
1415684_at 7.492504495
1415685_at 8.636340815
1415686_at 8.515230555
1415687_a_at 10.0278343
1415688_at 10.0052346
1415689_s_at 7.848280502

Total number of rows: 45101

Table truncated, full table size 1026 Kbytes.




Supplementary file Size Download File type/resource
GSM3966993_M9.CEL.gz 2.6 Mb (ftp)(http) CEL
Processed data included within Sample table

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