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Sample GSM4475144 Query DataSets for GSM4475144
Status Public on Jan 26, 2022
Title BM cells with RPMI, replicate 1
Sample type RNA
 
Source name BM cells cultured for 4h with RPMI
Organism Mus musculus
Characteristics strain background: Balb/c
cell type: BM cells
treatment: control in RPMI media
Treatment protocol cultured cells were lysed with TRIZOL and stored at -80◦C till RNA extraction was performed.
Growth protocol BM cells were harvested from the femur and tibia of Balb/c mice, ACK red cell lysis, and then were cultured for 4 hours in the presence of RPMI (10%FCS), RPMI supplemented with 30% of filtered supernatant from confluent 4T1 cultured with complete media, or RPMI supplemented with 30% of filtered supernatant from confluent 4T1 cultured with complete media and BX471 and Maraviroc.
Extracted molecule total RNA
Extraction protocol RNA was purified using the miRNA easy kit from Qiagen and following the manufacture instruction.
Label biotin
Label protocol Affymetrix GeneChip WT Terminal Labeling Kit - sense-strand cDNA is fragmented with a combination of uracil DNA glycosylase and apurinic/apyrimidinic endonuclease 1 and its yield is further labeled by terminal deoxynucleotidyl transferase (TdT) with the Affymetrix® proprietary DNA Labeling Reagent that is covalently linked to biotin.
 
Hybridization protocol GeneChip® Hybridization, Wash, and Stain Kit - Following labeling, 10 ug of cRNA were hybridized for 16 hr at 45C on GeneChip Human Gene 2.0 ST arrays. GeneChips were washed and stained (streptavidin,R-phycoerythrin conjugate and biotinylated anti-streptavidin) in the Affymetrix Fluidics Station 400.
Scan protocol Standard Affymetrix scanning procedures on a GeneChip® Scanner 3000 7G . Affymetrix GeneChip® Command Console® Software (AGCC)- used to view CEL file images.
Description Gene expression data of Balb/c BM cells cultured for 4h with RPMI
Data processing RMA of .CEL files using affy Bioconductor library. In RMA, PM values have been background adjusted, normalized using quantile normalization, and expression measure calculated using median polish summarization
 
Submission date Apr 14, 2020
Last update date Jan 26, 2022
Contact name Silvio Bicciato
E-mail(s) silvio.bicciato@unipd.it
Phone +39-049-827-6108
Organization name University of Padova
Department Molecular Medicine
Street address via U. Bassi 59/b
City Padova
ZIP/Postal code 35131
Country Italy
 
Platform ID GPL23092
Series (1)
GSE148615 Molecular and cellular characterization of MDSC differentiated from the bone marrow of Balb/c mice with tumor conditioned media or tumor conditioned media and antagonists for CCR1 and CCR5

Data table header descriptions
ID_REF
VALUE RMA-calculated signal intensity (log2)

Data table
ID_REF VALUE
100009600_at 4.28642159
100009609_at 2.578720467
100009614_at 3.845638328
100009664_at 3.352059913
100012_at 3.719919139
100017_at 8.563803801
100019_at 6.871390366
100033459_at 3.53433954
100034251_at 7.691470818
100034675_at 4.524302486
100034728_at 9.255839361
100034729_at 3.201842199
100034739_at 3.390656922
100034748_at 4.260165132
100036518_at 2.807846255
100036520_at 4.667223129
100036521_at 5.912051694
100036523_at 6.705197176
100036537_at 4.717097899
100036768_at 5.601419382

Total number of rows: 25428

Table truncated, full table size 538 Kbytes.




Supplementary file Size Download File type/resource
GSM4475144_pSearfini_BM-RPMI-24-1_Mouse2.0_01282016.CEL.gz 8.6 Mb (ftp)(http) CEL
Processed data included within Sample table

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