|
Status |
Public on Dec 01, 2013 |
Title |
Rickettsia rickettsii transcriptome - ch2: G1 replicate 2; ch1: G2 replicate 2 |
Sample type |
RNA |
|
|
Channel 1 |
Source name |
Temperature G2 Cy3
|
Organism |
Rickettsia rickettsii |
Characteristics |
strain: str. Taiaçu tissue: Pool of internal organs of 7 Amblyomma aureolatum female infected ticks group: G2; incubated at 35C for 3 days
|
Treatment protocol |
Right after molting to adult, not fed females of A. aureolatum were incubated at 35oC and 93% relative humidity (RH) for 3 days
|
Growth protocol |
Ticks were mainteined for 3 days at incubator conditons described above
|
Extracted molecule |
total RNA |
Extraction protocol |
Total RNA was extracted using Invitrap TwinSpin Cell Mini Kit (Stratec) and reverse transcribed using MessageAmp II Bacteria RNA Amplification Kit (Ambion)
|
Label |
Cy3
|
Label protocol |
Agilent's Genomic DNA ULS Labeling Kit
|
|
|
Channel 2 |
Source name |
Temperature G1 Cy5
|
Organism |
Rickettsia rickettsii |
Characteristics |
strain: str. Taiaçu tissue: Pool of internal organs of 7 Amblyomma aureolatum female infected ticks group: G1; incubated at 25C for 3 days
|
Treatment protocol |
Right after molting to adult, not fed females of A. aureolatum were incubated at 25oC and 93% relative humidity (RH) for 3 days
|
Growth protocol |
Ticks were mainteined for 3 days at incubator conditons described above
|
Extracted molecule |
total RNA |
Extraction protocol |
Total RNA was extracted using Invitrap TwinSpin Cell Mini Kit (Stratec) and reverse transcribed using MessageAmp II Bacteria RNA Amplification Kit (Ambion)
|
Label |
Cy5
|
Label protocol |
Agilent's Genomic DNA ULS Labeling Kit
|
|
|
|
Hybridization protocol |
Two-Color Microarray-Based Gene Expression Analysis Protocol
|
Scan protocol |
Fluorescent array images were collected for both Cy3 and Cy5 with a High-Resolution C Scanner (Agilent Technologies) using Agilent Settings and image intensity data were extracted with Feature Extraction 10.5 Software using Agilent Settings
|
Description |
R. rickettsii under 35oC X R. rickettsii under 25oC, experiment 4
|
Data processing |
Raw and background corrected data
|
|
|
Submission date |
Feb 14, 2013 |
Last update date |
Dec 01, 2013 |
Contact name |
Maria Fernanda Galletti |
E-mail(s) |
[email protected]
|
Organization name |
Universidade de São Paulo - Instituto de Ciências Biomédicas - Departamento de Parasitologia
|
Department |
Department of Parasitology
|
Lab |
Bioquemistry and Immunology of Arthropods
|
Street address |
Av. Prof. Lineu Prestes, 1374 sala 39
|
City |
São Paulo |
State/province |
São Paulo |
ZIP/Postal code |
05508-900 |
Country |
Brazil |
|
|
Platform ID |
GPL16681 |
Series (2) |
GSE44316 |
Rickettsia rickettsii transcriptome - Elevation of temperature response |
GSE44349 |
Natural blood feeding and temperature shift modulate the global transcriptional profile of Rickettsia rickettsii. |
|
Data table header descriptions |
ID_REF |
ID column of the reference platform |
gSignal |
Raw Median Signal of feature in green channel |
rSignal |
Raw Median Signal of feature in red channel |
gProcessedSignal |
Dye-normalized signal after surrogate algorithm,green channel,used for computation of log ratio. |
rProcessedSignal |
Dye-normalized signal after surrogate algorithm,red channel,used for computation of log ratio. |
VALUE |
log(gProcessedSignal/rProcessedSignal) representing (test/control) |
INV_VALUE |
log(rProcessedSignal/gProcessedSignal) |