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Sample GSM1561161 Query DataSets for GSM1561161
Status Public on Nov 02, 2015
Title normal lung parenchyma, biological rep2
Sample type RNA
 
Source name Normal lung parenchyma
Organism Mus musculus
Characteristics tissue: Normal lung parenchyma
histology: Normal lung parenchyma
strain: BalbC nude
Extracted molecule total RNA
Extraction protocol Tissue samples were laser captured using the MMI CellCut Plus (Molecular Machines & Industries, Glattbrugg Switzerland) as described in Golubeva et al 2013. Laser microdissected cells were lysed using the lysis buffer RLT from Qiagen Micro RNAeasy Kit (Qiagen Gaithersburg, MD) and total RNA lysates were prepared for NanoStrings analysis (Geiss et al 2008). In vitro JygMC(A) GFP/Luc cells were cultured either as monolayers in plates or 3D spheres on ultra-low adherent plates (third generation spheres). Total RNA from tissue samples was extracted using TRIzol reagent according to the manufacturer's recommendations (Invitrogen, Carlsbad, CA). Total RNA from cells was isolated and purified using the RNeasy Mini Kit and subjected to DNAse treatment (Qiagen, Gaithersburg, MD) in accordance to manufacturer instructions). Following extraction, 1ug of total RNA was reverse transcribed using the RETROscript® kit (Ambion, Carlsbad, CA) in accordance with manufacturer's instructions.
Label biotin
Label protocol The assays were performed according to the manufacturer’s instructions (NanoStrings Technologies, Seattle, WA)
 
Hybridization protocol The assays were performed according to the manufacturer’s instructions (NanoStrings Technologies, Seattle, WA)
Scan protocol The assays were performed according to the manufacturer’s instructions (NanoStrings Technologies, Seattle, WA)
Description normal lung parenchyma
Data processing Normalization was performed using the software nSolver version 1.1 (NanoStrings Technologies). The normalized counts were imported into the MultiExperiment Viewer Version 10.2 (MeV_4_8, http://www.tm4.org) software (Saeed et al 2003; 2006). The gene expression valuesProbe intensities were median-centered and log-transformed. Significant transcripts were selected using a t-test or the ANOVA statistical test with p <0.01 or 0.05. For clustering samples based on gene expression profile, we applied an unsupervised hierarchical clustering using Pearson correlation and average linkage.
 
Submission date Dec 08, 2014
Last update date Nov 02, 2015
Contact name David Salomon
E-mail(s) salomond@mail.nih.gov
Organization name NIH
Department NCI
Street address 1050 Boyles Drive, Bldg. 560 Room 1246
City Frederick
State/province MD
ZIP/Postal code 21701
Country USA
 
Platform ID GPL19518
Series (1)
GSE63951 Targeted mRNA gene expression profiling of primary tumors and lung metastases using a mouse model of spontaneous metastatic mammary carcinoma

Data table header descriptions
ID_REF
VALUE Normalized signal intensity

Data table
ID_REF VALUE
1 9208
2 11965
3 3303
4 5428
5 326
6 1530
7 11065
8 70
9 595
10 2063
11 373
12 765
13 25095
14 1796
15 2756
16 68
17 55
18 137603
19 7
20 163

Total number of rows: 118

Table truncated, full table size <1 Kbytes.




Supplementary file Size Download File type/resource
GSM1561161_20130228_20130228NDCc_34_N2_Lung_10.RCC.gz 2.3 Kb (ftp)(http) RCC
Processed data included within Sample table

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