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Sample GSM4743650 Query DataSets for GSM4743650
Status Public on Aug 25, 2020
Title Ly6C+ CD11b cult 2
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 45.1555
2900026A02Rik 13.2268
Abcc8 7.40466
Acad10 9.15098
Acly 675.234
Acod1 23.081
Acot11 13.2268
Acot3 13.2268
Acox1 234.066
Adam19 336.459
Adam8 3141.25
Adamts1 18.546
Adamts12 18.546
Adamts14 9.90369
Adamts17 21.8398
Adamts2 21.8398
Adamts3 23.081
Adamts4 13.2268
Adamts9 7.40466
Adcyap1r1 16.7731

Total number of rows: 734

Table truncated, full table size 9 Kbytes.




Supplementary file Size Download File type/resource
GSM4743650_20190809_Nano106car2_Ly6C_cult_2_11.RCC.gz 8.4 Kb (ftp)(http) RCC
Processed data included within Sample table

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