NCBI Logo
GEO Logo
   NCBI > GEO > Accession DisplayHelp Not logged in | LoginHelp
GEO help: Mouse over screen elements for information.
          Go
Sample GSM4743646 Query DataSets for GSM4743646
Status Public on Aug 25, 2020
Title CD11b Ly6C– cult 1
Sample type RNA
 
Source name Mus musculus
Organism Mus musculus
Characteristics strain: C57BL/6J
Sex: male
cell type: Ly-6C+ CD11b+ cDCs
Treatment protocol C57BL/6 mice were inhaled house dust extract (10 micrograms) together with ovalbumin (100 micrograms). Sixteen hours later, lungs were excised, and Ly-6C+CD11b+, Ly-6C– CD11b+, and CD103+ cDCs (CD11c+ I-A+ CD45+ CD88– Siglec-F– F4/80– Live/Dead–) and monocytes (CD45+ F4/80+ CD88– Siglec-F– I-A– Live/Dead–) were purified by flow cytometric sorting. Purified lung cDCs and monocytes (2×105 cells/200 μL/well) were cultured for 2 days in complete RPMI1640 medium containing 10% fetal bovine serum. Total RNA (50 ng of each ) was isolated from freshly isolated or cultured cells, and mRNA expression was examined using the NanoString platform utilizing the Mouse Myeloid Innate Immunity Panel v2.
Extracted molecule total RNA
Extraction protocol RNA was isolated from cells using Trizol, Dnase treated with Dnase I and further purified using Qiagen Rneasy mini kits. RNA concentration and purity was determined using a Qubit and Nanodrop.
Label na
Label protocol n/a
 
Hybridization protocol Reporter and Capture probes were added according to the manufacturer’s directions (nanostring.com) to 50 ng of total RNA in a final volume of 15ul followed by hybridization for at least 14 hours at 65oC
Scan protocol After sample processing according to manufacturer’s instructions on the nCounter Prep Station Model 5S, sample cartridges were scanned on an nCounter Digital Analyzer Model 5S, using 555 Fields of Vision (FOV) and the .rlf file 'Ns_Mm_Myeloid_v2'.
Data processing Data were adjusted utilizing the manufacturer’s positive and negative experimental control probes, as well as 2 HK genes (Sap130 and Sdha). All samples passed nSolver’s initial QA/QC controls. Compiled raw and data adjusted with positive/negative controls and the HK genes were exported as .csv files. nSolver adjusted data were then imported into Partek_v7.0 for further analysis
 
Submission date Aug 24, 2020
Last update date Aug 25, 2020
Contact name Rick David Fannin
E-mail(s) fannin@niehs.nih.gov
Phone 9842874069
Organization name Mr.
Department NIEHS/NIH
Lab Genomics Core
Street address 111 Tw Alexander Dr, MD D204
City RTP
State/province NC
ZIP/Postal code 27709
Country USA
 
Platform ID GPL25266
Series (1)
GSE156763 Gene expression of mouse lung CD11b+ dendritic cells before and after ex vivo culture

Data table header descriptions
ID_REF
VALUE Values are direct ‘counts’ of the number of gene specific epifluorescant dye barcodes in the scanned image.

Data table
ID_REF VALUE
2810417H13Rik 78.8093
2900026A02Rik 9.37696
Abcc8 9.37696
Acad10 9.37696
Acly 963.825
Acod1 10.7921
Acot11 19.705
Acot3 15.9366
Acox1 312.09
Adam19 896.711
Adam8 2282.83
Adamts1 22.9796
Adamts12 9.90369
Adamts14 14.1985
Adamts17 15.9366
Adamts2 24.516
Adamts3 26.3568
Adamts4 19.705
Adamts9 7.36968
Adcyap1r1 7.36968

Total number of rows: 734

Table truncated, full table size 9 Kbytes.




Supplementary file Size Download File type/resource
GSM4743646_20190809_Nano106car2_CDllb_cult_1_07.RCC.gz 8.4 Kb (ftp)(http) RCC
Processed data included within Sample table

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