|
Status |
Public on Dec 22, 2006 |
Title |
6microg/L_Cu_Exposed_rep1B |
Sample type |
RNA |
|
|
Channel 1 |
Source name |
whole organism, exposed 24-h to 6 microg/L Cu
|
Organism |
Daphnia magna |
Characteristics |
Daphnia magna: Aquatic Research Organisms Age: 15-18 days
|
Biomaterial provider |
Vulpe Lab
|
Treatment protocol |
24-h exposure to 6 microg/L Copper Sulfate
|
Growth protocol |
Genetically homogeneous Daphnia magna, purchased from Aquatic Research Organisms (Hampton, NH), were cultured in COMBO modified for water hardness (Kilham et al. 1998) and kept at 23.50 C in a Percival environmental chamber with a 16-hour light/ 8 hour dark cycle. The D. magna were maintained on a diet of YCT and Selenastrum capricornatum (Aquatic Research Organisms, Hampton, NH). Stock culture medium was renewed, cultures were fed, and neonates were separated from adults three times weekly.
|
Extracted molecule |
total RNA |
Extraction protocol |
Trizol method (invitrogen)
|
Label |
cy3
|
Label protocol |
see the protocols at the website of Dr. Patrick O. Brown's laboratory at Stanford University
|
|
|
Channel 2 |
Source name |
whole organism, unexposed
|
Organism |
Daphnia magna |
Characteristics |
Daphnia magna: Aquatic Research Organisms Age: 15-18 days
|
Biomaterial provider |
Vulpe Lab
|
Treatment protocol |
untreated 24 hours
|
Growth protocol |
Genetically homogeneous Daphnia magna, purchased from Aquatic Research Organisms (Hampton, NH), were cultured in COMBO modified for water hardness (Kilham et al. 1998) and kept at 23.50 C in a Percival environmental chamber with a 16-hour light/ 8 hour dark cycle. The D. magna were maintained on a diet of YCT and Selenastrum capricornatum (Aquatic Research Organisms, Hampton, NH). Stock culture medium was renewed, cultures were fed, and neonates were separated from adults three times weekly.
|
Extracted molecule |
total RNA |
Extraction protocol |
Trizol method (Invitrogen)
|
Label |
cy5
|
Label protocol |
see the protocols at the website of Dr. Patrick O. Brown's laboratory at Stanford University
|
|
|
|
Hybridization protocol |
see the protocols at the website of Dr. Patrick O. Brown's laboratory at Stanford University
|
Scan protocol |
Scanning was performed using an arrayWoRx Biochip Reader (Applied Precision, Issaquah, WA)
|
Description |
none
|
Data processing |
Signal intensities determined by GenePix software version 3.01 (Axon Instruments, Union City, CA)
|
|
|
Submission date |
May 02, 2006 |
Last update date |
Dec 22, 2006 |
Contact name |
Helen C Poynton |
E-mail(s) |
helen.poynton@umb.edu
|
Phone |
617-287-7323
|
Organization name |
UMass Boston
|
Department |
School for the Environment
|
Lab |
Poynton Lab
|
Street address |
100 Morrissey Blvd.
|
City |
Boston |
State/province |
MA |
ZIP/Postal code |
02125 |
Country |
USA |
|
|
Platform ID |
GPL3710 |
Series (1) |
GSE4759 |
1/10 LC50 metal exposures to Daphnia magna |
|