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Sample GSM6762163 Query DataSets for GSM6762163
Status Public on Feb 14, 2023
Title KAE609, Time 24h, Rep 3
Sample type RNA
 
Source name KA09-treated Dd2-A211V, Time 24, Rep 3
Organism Plasmodium falciparum
Characteristics tissue: Blood-stage Dd2-A211V P. falciparum parasites cultured in human erythrocytes at 2% hematocrit and 30 pM KAE609
time: 24h
replicate: Rep 3
Treatment protocol Sublethal doses of KAE609 (30 pM) or PA21A092 (400 nM) was added to control RPMI medium at 0 h of the experiment, which was determined using blood smears of the parasite cultures (described in the paper).
Extracted molecule total RNA
Extraction protocol For each data point, RNA was extracted from 50 µL of packed RBC culture with Trizol Reagent and the PureLink Mini Kit (Invitrogen/Thermo Fisher Scientific). 1ml Trizol was added to each sample, followed by high-speed disruption in tubes containing Lysing Matrix D (MP Biomedical) in a FastPrep 120 Instrument at speed 6 for 20 seconds. Homogenates were subsequently processed according to the PureLink Mini Kit manufacturer’s (Invitrogen/Thermo Fisher Scientific) protocol, including on-column DNase treatment.
Label Cy3
Label protocol From 100 ng of total RNA, Cyanine-3 labeled cRNA was prepared using the Low Input Quick Amp Labeling Kit One-Color (Agilent).
 
Hybridization protocol The eight time course samples were hybridized (along with the manufacturer’s RNA spike-in controls) according to standard protocol to the 8 sectors of an Agilent 8x15K platform microarray (AMADID 037237) with separate microarray slides used for each biological replicate.
Scan protocol Arrays were scanned with the Agilent G2600D SureScan microarray scanner using scan protocol AgilentHD_GX_1color. Agilent’s Feature Extraction Software was used to assign grids, provide raw image files per array, and generate QC metric reports from the microarray scan data.
Description Gene expression data
Data processing Txt files from Agilent’s Feature Extraction Software were transferred to Partek Genomics Suite software (v7.0). Within Partek, the gProcessedSignal was imported and the intensity values were normalized using Quantile Normalization and Log Tranformation Base 2.0 after import.
 
Submission date Nov 29, 2022
Last update date Feb 15, 2023
Contact name Shivendra G Tewari
E-mail(s) stewari@bhsai.org
Phone 3016191942
Organization name Biotechnology HPC Software Applications Institute
Street address 2405 Whittier Drive, Suite 200
City Frederick
State/province MD
ZIP/Postal code 21702
Country USA
 
Platform ID GPL27130
Series (1)
GSE218998 Metabolic responses in blood-stage malaria parasites associated with increased and decreased sensitivity to PfATP4 inhibitors

Data table header descriptions
ID_REF
VALUE Normalized signal intensity

Data table
ID_REF VALUE
PFL0815w 11.8716
PFB0495w 5.69694
PF13_0050 8.98971
PF14_0416 10.4849
PF11_0120 8.55175
PFI1280c 7.93554
MAL8P1.65 8.96472
PF10_0356 1.52592
PFD0265w 9.69451
PF11_0123 6.67793
PFE1170w 7.51601
PFB0080c 0.344824
PF14_0045 7.75351
PFL2245w 11.6414
PF11_0482 5.48358
PF13_0354 10.136
eGFP_mut2 0.337007
MAL8P1.57 8.9288
PFB0125c 6.33383
PF10_0378 1.71726

Total number of rows: 5851

Table truncated, full table size 102 Kbytes.




Supplementary file Size Download File type/resource
GSM6762163_253723710248_Time_24_Dd2KAE609_Rep_3_1_4.txt.gz 771.3 Kb (ftp)(http) TXT
Processed data included within Sample table

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