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Sample GSM4743633 Query DataSets for GSM4743633
Status Public on Aug 25, 2020
Title CD103 fresh 3
Sample type RNA
 
Source name Mus musculus
Organism Mus musculus
Characteristics strain: C57BL/6J
Sex: male
cell type: conventional dendritic cells
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) [email protected]
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 290.367
2900026A02Rik 29.8248
Abcc8 15.5357
Acad10 25.21
Acly 979.208
Acod1 7.50337
Acot11 81.6668
Acot3 19.92
Acox1 188.474
Adam19 502.081
Adam8 2977.46
Adamts1 7.50337
Adamts12 7.50337
Adamts14 7.50337
Adamts17 12.7942
Adamts2 19.92
Adamts3 14.6488
Adamts4 7.50337
Adamts9 7.50337
Adcyap1r1 9.38135

Total number of rows: 734

Table truncated, full table size 9 Kbytes.




Supplementary file Size Download File type/resource
GSM4743633_20190809_Nano106car1_CD103_fresh_3_03.RCC.gz 8.5 Kb (ftp)(http) RCC
Processed data included within Sample table

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