|
Status |
Public on Dec 31, 2013 |
Title |
7420068_AOM/DSS d65 |
Sample type |
RNA |
|
|
Channel 1 |
Source name |
Universal Reference (Miltenyi Biotec GmbH)
|
Organism |
synthetic construct |
Characteristics |
reference: syntethic miRNA pool of 954 synthetic miRNAs in equimolar concentrations from human, mouse, rat, and virus
|
Treatment protocol |
AOM 12 mg/kg in PBS, one intraperitoneal injection at day 1. DSS 2% in drinkable water, 3 cycles administration of 5 days followed by 16 days recovery. Fisrt day of first DSS cycle at day 7.
|
Extracted molecule |
total RNA |
Extraction protocol |
RNA were extracted from the whole colon with 8 mL Tripur according to the manufacturer's instructions.
|
Label |
Hy3
|
Label protocol |
2 µg of respective total RNA as well as 2 fmol of the Universal Reference (Miltenyi Biotec GmbH) were each mixed with 2.5 fmol of each of 18 RNA oligonucleotides reverse complement to miRControl 3 probes and subsequently fluorescently labeled using a commercial kit (miRCury™ LNA microRNA Array Power labeling kit, Exiqon) following the instructions of the manufacturer. The total RNA and Universal Reference mix was hybridized in a dual colour approach to miRXplore™ microarrays (Miltenyi Biotec GmbH).
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|
|
Channel 2 |
Source name |
AOM/DSS d65
|
Organism |
Mus musculus |
Characteristics |
strain: C57bl6 tissue: Whole colonic tissue treatment: AOM/DSS treated-mice for 65 days
|
Treatment protocol |
AOM 12 mg/kg in PBS, one intraperitoneal injection at day 1. DSS 2% in drinkable water, 3 cycles administration of 5 days followed by 16 days recovery. Fisrt day of first DSS cycle at day 7.
|
Extracted molecule |
total RNA |
Extraction protocol |
RNA were extracted from the whole colon with 8 mL Tripur according to the manufacturer's instructions.
|
Label |
Hy5
|
Label protocol |
2 µg of respective total RNA as well as 2 fmol of the Universal Reference (Miltenyi Biotec GmbH) were each mixed with 2.5 fmol of each of 18 RNA oligonucleotides reverse complement to miRControl 3 probes and subsequently fluorescently labeled using a commercial kit (miRCury™ LNA microRNA Array Power labeling kit, Exiqon) following the instructions of the manufacturer. The total RNA and Universal Reference mix was hybridized in a dual colour approach to miRXplore™ microarrays (Miltenyi Biotec GmbH).
|
|
|
|
Hybridization protocol |
Hy3 and Hy5 labeled (sample_ch1 and sample_ch2) RNA were combined and hybridized overnight to miRXplore™ microarrays (Miltenyi Biotec GmbH) using the a-Hyb™ Hybridization Station (Miltenyi Biotec)
|
Scan protocol |
Image capture and signal quantification of hybridized miRXplore™ microarrays microarrays were done with the Agilent’s Microarray Scanner System (G2505C, Agilent Technologies, Palo Alto, USA) and ImaGene software Version 8.0.1 (BioDiscovery, Los Angeles, CA, USA).
|
Description |
0007420068_raw biological replicate 5 of 5. Fourth point of 4 time points. Tumours present
|
Data processing |
Signal quantification was done using ImaGene software version 8.0.1 (BioDiscovery, Los Angeles, MA). Median normalization was performed using the calibration oligos
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|
|
Submission date |
Jun 04, 2012 |
Last update date |
Dec 31, 2013 |
Contact name |
Claire Josse |
E-mail(s) |
[email protected]
|
Phone |
+32 4 366 25 74
|
Organization name |
CHU Liege
|
Department |
Medical Oncology
|
Lab |
Human Genetics
|
Street address |
rue de l'hopital, 1
|
City |
Liège |
State/province |
Liège |
ZIP/Postal code |
4000 |
Country |
Belgium |
|
|
Platform ID |
GPL15644 |
Series (1) |
GSE38443 |
Identification of microRNA landscape of inflammation-induced colorectal carcinogenesis |
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