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Sample GSM1832260 Query DataSets for GSM1832260
Status Public on Jul 28, 2015
Title D7_0__B
Sample type RNA
 
Source name Macroschizont
Organism Theileria annulata
Characteristics infected host cell line: Bos taurus (bovine) lymphosarcoma cell line
differentiation time-point: Day 0
parasite strain: D7
Treatment protocol Stimulation of cells was carried out for up to 48 hours in six well plates with 5,000,000 cells/well in a total of 5 ml medium, set up immediately prior to addition of 1 μg/ml LPS (Sigma: L2630).
Growth protocol BL20, an uninfected bovine lymphosarcoma cell line (Olobo and Black, 1989. Vet. Immunol. Immunopathol. 20, 165-172) and TBL20, a T. annulata (Ankara strain) infected BL20 cell line (Shiels et al., 1986. Vet. Parasitol. 21, 1-10.) were cultured in standard complete medium (Swan et al., 1999. Mol. Biochem. Parasitol. 101, 117-129) except that heat-inactivated foetal bovine serum (FBS; Sigma) was used. Cultures were seeded with 200,000 cells/ml and maintained by feeding with fresh medium every two to three days (Schmuckli-Maurer et al., 2010. Cell Microbiol. 12, 158-173).
Extracted molecule total RNA
Extraction protocol Total RNA was extracted using Triazol (ref) and this was cleaned up using an RNeasy Mini kit (Qiagen Inc., CA, USA) . RNA quality and concentration was determined by analysis with an Agilent 2100 bioanalyzer (ref)
Label Cy3
Label protocol Labeling was performed by NimbleGen Systems Inc., Madison, WI USA, following their standard operating protocol. See www.nimblegen.com.
 
Hybridization protocol Hybridization was performed by NimbleGen Systems Inc., Madison, WI, USA following their standard operating protocol. See www.nimblegen.com.
Scan protocol Scanning was performed by NimbleGen Systems Inc., Madison, WI USA, following their standard operating protocol. See www.nimblegen.com.
Description This sample is of a T. annulata infected cell line maintained at 37oC (2 of 3)
Data processing The raw data (.pair file) was subjected to RMA (Robust Multi-Array Analysis; Irizarry et al. Biostatistics 4(2):249), quantile normalization (Bolstad et al. Bioinformatics 19(2):185), and background correction as implemented in the NimbleScan software package, version 2.4.27 (Roche NimbleGen, Inc.).
 
Submission date Jul 24, 2015
Last update date Jul 28, 2015
Contact name William Weir
Organization name University of Glasgow
Department Institute of Infection, Immunity and Inflammation
Lab Theileria lab
Street address Room 220, Henry Wellcome Building, Garscube Campus, Bearsden Road
City Glasgow
ZIP/Postal code G61 1QH
Country United Kingdom
 
Platform ID GPL20733
Series (1)
GSE71307 ApiAP2 Factors as Candidate Regulators of Stochastic Commitment to Merozoite Production in Theileria annulata

Data table header descriptions
ID_REF
VALUE RMA-normalized, averaged gene-level signal intensity

Data table
ID_REF VALUE
TA09775 8.4401
TA09785 13.2662
TA09790 12.4873
TA09795 15.1017
TA09800 12.3285
TA09805 13.4558
TA09810 12.2845
TA09865 13.6497
TA09920 11.8676
TA09975 9.0876
TA10030 10.3687
TA10085 13.5296
TA10090 11.4264
TA10195 11.3184
TA10200 10.9963
TA10305 11.5905
TA10310 13.2778
TA10365 13.1513
TA10420 11.422
TA10475 9.5302

Total number of rows: 3802

Table truncated, full table size 58 Kbytes.




Supplementary file Size Download File type/resource
GSM1832260_2935802_532_pair.txt.gz 5.2 Mb (ftp)(http) TXT
Processed data included within Sample table

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