|
Status |
Public on Nov 01, 2011 |
Title |
Cardiomyocyte control_mRNA content_rep2 |
Sample type |
RNA |
|
|
Source name |
Cardiomyocyte control_mRNA content
|
Organism |
Mus musculus |
Characteristics |
cell type: cardiomyocyte cell line: HL-1
|
Growth protocol |
Cultured cardiomyocytes in claycomb medium in 37 degrees, 5% CO2
|
Extracted molecule |
total RNA |
Extraction protocol |
Cardiomyocytes were put in RNAlater, Qiagen miRNEasy Mini Kit was used to extract total RNA. Sigma GenElute Mammalian Genomic DNA Miniprep Kit were used to extract DNA. Terminal deoxynucleotidyl transferase were used to add a poly_T tail to DNA from microvesicles to construct cDNA, possible to label as cRNA and use on the chip to identify part of the sequence of the original DNA.
|
Label |
Cy3
|
Label protocol |
Illumina TotalPrep RNA Amplification Kit was used. Terminal deoxynucleotidyl transferase were used to add a poly-T tail to DNA from microvesicles to construct cDNA, possible to label as cRNA and bind to chip.
|
|
|
Hybridization protocol |
Performed according to Illumina protocol
|
Scan protocol |
Illumina Beadstation 500GX according to Illumina protocol
|
Description |
total RNA->cRNA Chip sample 4613963055_G
|
Data processing |
Gene expression analysis (not differential) Cubic spline normalization, subtracted background, False Discovery Rate. Illumina Beadstudio 3.3 was used with gene expression module 3.4.0
|
|
|
Submission date |
May 06, 2010 |
Last update date |
Nov 01, 2011 |
Contact name |
Urban Hellman |
E-mail(s) |
urban.hellman@medbio.umu.se
|
Phone |
+46907851621
|
Organization name |
Umea University
|
Department |
Public health and clinical medicine
|
Street address |
Nus 6M
|
City |
Umea |
ZIP/Postal code |
90185 |
Country |
Sweden |
|
|
Platform ID |
GPL6885 |
Series (1) |
GSE21707 |
Identification of cardiomyocyte-derived microvesicles content. |
|