|
| Status |
Public on Jul 01, 2012 |
| Title |
Plasmodium falciparum, parasite control, B |
| Sample type |
RNA |
| |
|
| Source name |
Plasmodium falciparum FCR3, parasite control
|
| Organism |
Plasmodium falciparum |
| Characteristics |
strain: FCR3
csa adhesion: yes
developmental stage: 24h after late trophozoite stage
|
| Treatment protocol |
Prior to each experiment, FCR3CSA parasites were selected for chondroitin sulfate A (CSA) adhesion by panning. Both strains were constantly synchronized with 5% sorbitol and mature trophozoite-infected erythrocytes (iRBCs) were purified by magnetic cell sorting LD columns (MACS; Miltenyi Biotec). After 24 hours culture of FCR3CSA-infected erythrocytes at 37ºC in 5% CO2, RNA was extracted.
|
| Growth protocol |
FCR3CSA was maintained in continuous culture as described by Trager and Jensen.
|
| Extracted molecule |
total RNA |
| Extraction protocol |
RNA was isolated with Trizol according to manufacturer's instructions.
|
| Label |
biotin
|
| Label protocol |
Standard Affymetrix labeling protocol.
|
| |
|
| Hybridization protocol |
Standard Affymetrix Hybridization Protocol.
|
| Scan protocol |
Standard Affymetrix Scanning Protocol.
|
| Description |
Control culture.
|
| Data processing |
Signals were normalized using GC-RMA.
|
| |
|
| Submission date |
Nov 13, 2009 |
| Last update date |
Jul 01, 2012 |
| Contact name |
Evelyn Boettger |
| E-mail(s) |
evelyn-boettger@hotmail.de
|
| Organization name |
Institute of Tropical Medicine
|
| Street address |
Wilhelmstrasse 27
|
| City |
Tuebingen |
| ZIP/Postal code |
72074 |
| Country |
Germany |
| |
|
| Platform ID |
GPL1321 |
| Series (1) |
| GSE19010 |
Gene expression profiling of Plasmodium falciparum after co-culture with NK cells |
|
