|
| Status |
Public on Jul 25, 2017 |
| Title |
mouse_blood_control |
| Sample type |
RNA |
| |
|
| Source name |
mouse blood control
|
| Organism |
Mus musculus |
| Characteristics |
tissue: blood
|
| Treatment protocol |
the control line and experiment line includes 3 replicates, the heat-induced ones are pretreatment in waterbath for 1h at 37℃,then moved to 38.5℃ for 1h
|
| Extracted molecule |
total RNA |
| Extraction protocol |
RNA was prepared using the Versagene Blood RNA Purification kit (Gentra Systems, Minneapolis MN) following the manufacturer's recommendations. The protocol includes differential lysis of red and white blood cells, and an on-column DNase digestion. Globin message was further reduced using GLOBINclear (Ambion Inc., Austin, TX) to specifically remove both a- and b- globin. RNA was quantified using a NanoDrop-1000 spectrophotometer and quality was monitored with the Agilent 2100 Bioanalyzer (Agilent Technologies, Santa Clara, CA).
|
| Label |
Cy3
|
| Label protocol |
Cyanine-3 (Cy3) labeled cRNA was prepared from 0.5 ug RNA using the One-Color Low RNA Input Linear Amplification PLUS kit (Agilent) according to the manufacturer's instructions, followed by RNAeasy column purification (QIAGEN, Valencia, CA). Dye incorporation and cRNA yield were checked with the NanoDrop ND-1000 Spectrophotometer.
|
| |
|
| Hybridization protocol |
1.5 ug of Cy3-labelled cRNA (specific activity >10.0 pmol Cy3/ug cRNA) was fragmented at 60°C for 30 minutes in a reaction volume of 250 ml containing 1x Agilent fragmentation buffer and 2x Agilent blocking agent following the manufacturers instructions. On completion of the fragmentation reaction, 250 ml of 2x Agilent hybridization buffer was added to the fragmentation mixture and hybridized to Agilent Whole Human Genome Oligo Microarrays (G4112A) for 17 hours at 65°C in a rotating Agilent hybridization oven. After hybridization, microarrays were washed 1 minute at room temperature with GE Wash Buffer 1 (Agilent) and 1 minute with 37°C GE Wash buffer 2 (Agilent), then dried immediately by brief centrifugation.
|
| Scan protocol |
Slides were scanned immediately after washing on the Agilent DNA Microarray Scanner (G2505B) using one color scan setting for 1x44k array slides (Scan Area 61x21.6 mm, Scan resolution 10um, Dye channel is set to Green and Green PMT is set to 100%).
|
| Data processing |
The scanned images were analyzed with Feature Extraction Software 9.1 (Agilent) using default parameters (protocol GE1-v1_91 and Grid: 012391_D_20060331) to obtain background subtracted and spatially detrended Processed Signal intensities. Features flagged in Feature Extraction as Feature Non-uniform outliers were excluded.
|
| |
|
| Submission date |
Jul 24, 2017 |
| Last update date |
Jan 23, 2018 |
| Contact name |
Dean Liu |
| E-mail(s) |
2130734946@qq.com
|
| Phone |
86-15856907521
|
| Organization name |
OE biotech
|
| Department |
Bioinformatics
|
| Street address |
new ring road 138,minghang area
|
| City |
shanghai |
| State/province |
shanghai |
| ZIP/Postal code |
201114 |
| Country |
China |
| |
|
| Platform ID |
GPL21163 |
| Series (1) |
| GSE101787 |
Analysis of the gene expression of the mouse after different heat-induced treatment |
|
