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Status |
Public on Feb 22, 2016 |
Title |
In-vitro iHep mHSC, rep 2 |
Sample type |
RNA |
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Source name |
In-vitro iHep mHSC
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Organism |
Mus musculus |
Characteristics |
strain/background: Balb/c AnNCrl cell type: in-vitro myofibroblasts-derived induced hepatocytes reprogrammed: yes
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Extracted molecule |
total RNA |
Extraction protocol |
Total RNA was extracted from the cells.
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Label |
Alexa Fluor 555
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Label protocol |
100 ng of total DNA-free RNA was used as input to prepare the aminoallyl-UTP-modified (aaUTP) cRNAs (Amino Allyl MessageAmp II Kit, #AM1753, Life Technologies) as directed by the company. The aaUTP-cRNAs were labelled with Alexa Fluor 555 Reactive Dye (#A32756, LifeTechnologies). Prior to the reverse transcription reaction, 1μl of a 1:5000 dilution of Agilent's One-Color spike-in Kit stock solution (#5188-5282, Agilent Technologies) was added to 100ng of total RNA of each analyzed sample.
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Hybridization protocol |
The cRNA fragmentation, hybridization, and washing steps were carried out according to Agilent's One-Color Microarray-Based Gene Expression Analysis Protocol V5.7 except that 500ng of each labelled cRNA sample were used for hybridization.
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Scan protocol |
Slides were scanned on the Agilent Micro Array Scanner G2565 CA (pixel resolution 5 micrometers, bit depth 20). Data extraction was performed with the Feature Extraction Software V10.7.3.1.
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Description |
Replicate 2
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Data processing |
Variance stabilization was performed using the log2 scaling and gene expression normalization was calculated with the quantile method implemented in the lumi package of R-Bioconductor. Data post-processing and graphics were performed with in-house developed functions in MATLAB. Hierarchical clusters of genes and samples were performed with the one minus the sample correlation metric and the Unweighted Pair-Group Method using Average (UPGMA) linkage method.
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Submission date |
Jan 13, 2016 |
Last update date |
Jan 15, 2022 |
Contact name |
Marcos J. Araúzo-Bravo |
E-mail(s) |
mararabra@yahoo.co.uk
|
Phone |
+34 943 00 6108
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Organization name |
Max Planck Institute for Molecular Biomedicine
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Department |
Cell and Developmental Biology
|
Lab |
Computational Biology and Bionformatics
|
Street address |
Rogentstrasse
|
City |
Muenster |
ZIP/Postal code |
48149 |
Country |
Germany |
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|
Platform ID |
GPL11202 |
Series (1) |
GSE76843 |
Direct reprogramming of hepatic myofibroblasts into hepatocytes in vivo attenuates liver fibrosis |
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