NCBI Logo
GEO Logo
   NCBI > GEO > Accession DisplayHelp Not logged in | LoginHelp
GEO help: Mouse over screen elements for information.
          Go
Sample GSM1373911 Query DataSets for GSM1373911
Status Public on Jan 01, 2016
Title C_2
Sample type RNA
 
Source name Cell culture, replicate 2
Organism Mus musculus
Characteristics strain: C57BL/6
age: 8-12 week old mice
tissue: heart left atrial appendage
Growth protocol Adult (8-12 weeks old) C57BL/6 mice were deeply anesthetized with isoflurane and left atrial appendages were removed. The explants were then digested three times (5min) with trypsin & collagenase D. Strong enzyme digestion was performed with trypsin 0.25% and collagenase D 0.1% and alternatively, weak enzyme digestion with trypsin 0.05% and collagenase D 0.1%. After digestion the explants were placed on 24 –well plates (tissue culture treated) in culture medium (CEM: Isocove’s modified Dulbecco’s Medium with 25mM HEPES, supplemented with 10% FBS (fetal bovine serum), 1% L-glutamine, 1% penicillin-streptomycin & 0.1mM 2 -mercaptoethanol).
Extracted molecule total RNA
Extraction protocol Total RNA of cultured cells was extracted with High Pure RNA isolation kit (Roche) according to the manufacturer’s instructions. RNA -sample quality and integrity was tested with Bioanalyzer 2100 (Agilent Technologies). RNA from control tissue samples was isolated using Tri-reagent.
Label Cy3
Label protocol 200 ng of total RNA for each sample was amplified and labeled with a fluorescent dye (Cy3 ) using the Low RNA Input Linear Amplification & Labeling kit (Agilent ).
 
Hybridization protocol The Cy3 labeled cRNA was hybridized to the 8 X 60K Agilent Whole Mouse Genome Oligo Microarray V2 (design 028005 Agilent Technologies, USA) for 17 hours at 65°C in an Agilent DNA-Microarray Hybridization Oven.
Scan protocol The Microarray was scanned using the Agilent High-Resolution Microarray Scanner.
Description 8th passage derivates from c-kit+/CD45+ cells
C
Data processing Data was extracted from the resulting images using the Feature Extraction 10.7 software.
 
Submission date Apr 24, 2014
Last update date Jan 01, 2016
Contact name Jussi Leinonen
E-mail(s) jussi.leinonen@mac.com
Organization name Hadassah-Hebrew University Medical Center
Department Cardiovascular Research Center, Heart Institute
Street address Kiryat Hadassah p.o.b 12000
City Jerusalem
ZIP/Postal code 91120
Country Israel
 
Platform ID GPL13912
Series (2)
GSE57064 Macrophage Precursor Cells from the Left Atrial Appendage of the Adult Heart Spontaneously Reprogram into a C-kit+/CD45- Stem Cell-Like Phenotype [Array analysis]
GSE57126 Macrophage Precursor Cells from the Left Atrial Appendage of the Adult Heart Spontaneously Reprogram into a C-kit+/CD45- Stem Cell-Like Phenotype

Data table header descriptions
ID_REF
VALUE Background corrected, quantile normalized, spot intensities

Data table
ID_REF VALUE
1 14.72432712
2 4.527688162
3 4.150414235
4 5.002767389
5 6.301427351
6 5.390069414
7 5.011179906
8 11.64866484
9 4.463810848
10 5.440768819
11 6.131779766
12 4.738146063
13 8.789521363
14 13.12720785
15 6.038836976
16 4.897837557
17 11.73551477
18 8.699667819
19 11.39531455
20 15.01837934

Total number of rows: 62976

Table truncated, full table size 1090 Kbytes.




Supplementary file Size Download File type/resource
GSM1373911_US10023759_252800513284_S01_GE1_107_Sep09_2_2.txt.gz 12.0 Mb (ftp)(http) TXT
Processed data included within Sample table

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