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Sample GSM8084255 Query DataSets for GSM8084255
Status Public on Sep 15, 2024
Title BM_WT1_Mono
Sample type RNA
 
Source name bone marrow
Organism Mus musculus
Characteristics strain: C57/Bl6
cell type: Mono
mouse id: WT1
Treatment protocol Femurs were flushed with PBS, bone marrow cells were stained with lineage markers for NECs, PMNs, and Monos for 30 minutes at 4 °C. On average, 2 x 106 NECs, 1 x 106 PMNs, and 0.5 x 106 Monos were sorted using a FACSAria II instrument (BD Biosciences, Germany). Sorted populations were snap-frozen on dry ice and stored at -80°C.
Growth protocol ACKR1-deficient mice generated with 129P2/OlaHsd ES cells were backcrossed for more than 10 generations onto a C57BL/6J background and maintained as a heterozygous breed. All experimental procedures were performed with 8- to 12-week-old male mice.
Extracted molecule total RNA
Extraction protocol RNA extraction was carried out using the RNeasy Mini Kit (Qiagen, Germany) following the manufacturer's instructions.
Label Biotin
Label protocol The preparation of fragmented Biotin-labeled sense-strand cDNA was carried out using the Affymetrix GeneChip® WT PICO Reagent kit (ThermoFisher, Germany) following the manufacturer's instructions. 2 ng total RNA per sample was spiked with polyadenylated transcripts, subjected to reverse transcription into cDNA, and subsequently converted into cRNA through in vitro transcription.
 
Hybridization protocol cRNA (> 20 µg) was subjected to hybridization at 45 °C for 16 hours on separate Affymetrix Clariom D Arrays for Mouse, previously known as Affymetrix Mouse Transcriptome Array 1.0 (ThermoFisher, Germany). Microarrays underwent two binding cycles involving anti-Biotin antibodies and a Streptavidin-phycoerythrin conjugate.
Scan protocol GeneChips were scanned using Affymetrix GeneChip® 3000 Scanner (ThermoFisher, Germany).
Description Gene expression data from murine bone marrow nucleated erythroid cells (NEC), monocytes (Mono), and polymorphonuclear neutrophils (PMN)
Data processing Probe intensities were analyzed with Transcriptome Analysis Console (TAC) software v4.0.2 (ThermoFisher, Germany) following an assessment of quality control metrics. Affymetrix probes were annotated to the mouse genome GRCm38/mm10. Analysis was conducted with TAC default settings and quantile normalization method.
 
Submission date Feb 16, 2024
Last update date Sep 15, 2024
Contact name Johan Duchene
E-mail(s) [email protected], [email protected]
Phone +4989440054757
Organization name LMU
Department IPEK
Street address Pettenkoferstrasse, 9
City Munich
State/province - Please Select -
ZIP/Postal code 80336
Country Germany
 
Platform ID GPL20775
Series (1)
GSE256021 129-derived passenger mutations confound phenotype of ACKR1-deficient mice

Data table header descriptions
ID_REF
VALUE Generated CEL files were analyzed using Affymetrix Analysis Console v. 4.0.2 and the SST-RMA method was applied.

Data table
ID_REF VALUE
TC0100000001.mm.1 4.55
TC0100000002.mm.1 4.5
TC0100000003.mm.1 4.94
TC0100000004.mm.1 6.09
TC0100000005.mm.1 4.05
TC0100000006.mm.1 4.43
TC0100000007.mm.1 3.8
TC0100000008.mm.1 8.98
TC0100000009.mm.1 4.59
TC0100000011.mm.1 5.34
TC0100000012.mm.1 3.35
TC0100000013.mm.1 4.2
TC0100000014.mm.1 9.31
TC0100000015.mm.1 7.43
TC0100000016.mm.1 5.7
TC0100000017.mm.1 4.1
TC0100000018.mm.1 4.03
TC0100000019.mm.1 4.65
TC0100000020.mm.1 3.56
TC0100000021.mm.1 9.33

Total number of rows: 65956

Table truncated, full table size 1482 Kbytes.




Supplementary file Size Download File type/resource
GSM8084255_16129-0003.CEL.gz 24.3 Mb (ftp)(http) CEL
Raw data provided as supplementary file
Processed data included within Sample table

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