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Sample GSM570451 Query DataSets for GSM570451
Status Public on Jul 27, 2010
Title 11P T, biological rep2
Sample type RNA
 
Source name Mutant 11P, tachyzoites
Organism Toxoplasma gondii
Characteristics strain: RH strain
Growth protocol T. gondii tachyzoites were maintained by serial passage in primary cultures of Human foreskin fibroblast (HFF) cells. Parasites were induced to differentiate into bradyzoites in low [CO2], resulting in pyrimidine starvation. CO2 depletion was accomplished by inoculating tachyzoites in host cells in minimal essential medium without NaHCO3 but containing 25 mM HEPES.
Extracted molecule total RNA
Extraction protocol Total RNA was extracted with the Qiagen kit according to the manufacturer's instructions.
Label biotin
Label protocol RNA amplification, fragmentation, and labeling were performed using the Ovation V2 and Encore reagents by NuGEN technologies.
 
Hybridization protocol GeneChip hybridization mixes were prepared using 4ug of the biotin-labeled fragmented cDNA and hybridized to the ToxoGeneChip array as per manufacturer’s recommendations for 16 hr at 45C at 60 rpm, double stained with streptavidin-PE using the Affymetrix 450 fluidics station.
Scan protocol GeneChips were scanned with the Affymetrix 3000-G7 scanner.
Description DHF-T-D-matrajt-070607-tox.CEL
Data processing Raw GeneChip data includes a collection of images, one for each probe and chip. Each image is summarized by Affymetrix GCOS software using one probe intensity (in CEL files, one per chip). We calculated a summary measure of expression, for each probe set, using the Robust Multichip Average (RMA) method using R and BioConductor tools (aroma.affymetrix package of Bengtesson).
 
Submission date Jul 26, 2010
Last update date Jan 24, 2013
Contact name Mariana Matrajt
E-mail(s) [email protected]
Organization name University of Vermont
Street address 95 Carrigan Drive
City Burlington
ZIP/Postal code 05405
Country USA
 
Platform ID GPL16542
Series (1)
GSE23174 Expression data from Toxoplasma gondii mutants and wild-type during bradyzoite differentiation in vitro

Data table header descriptions
ID_REF
VALUE log2 RMA signal

Data table
ID_REF VALUE
1.m00014_at 12.17664842
10.m00080_s_at 8.195501304
10.m00081_at 3.943052472
100.m00002_at 6.748722579
100.m00002_x_at 5.232395442
107.m00007_s_at 4.483993276
107.m00010_at 3.682800485
108.m00006_at 3.80820136
108.m00006_x_at 3.743087242
113.m00001_at 9.252515114
113.m00009_at 10.42612594
113.m00012_at 11.05216317
113.m00015_at 7.226699221
113.m00016_at 12.77801273
113.m00753_at 5.345131295
113.m00755_at 11.69978148
113.m00756_at 9.025447477
113.m00757_at 7.633344883
113.m00758_at 5.065187411
113.m00760_at 9.994274041

Total number of rows: 8993

Table truncated, full table size 220 Kbytes.




Supplementary file Size Download File type/resource
GSM570451.CEL.gz 1005.7 Kb (ftp)(http) CEL
Processed data included within Sample table

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