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Sample GSM2700788 Query DataSets for GSM2700788
Status Public on Oct 16, 2018
Title U937 300s microgravity rep2
Sample type RNA
 
Source name U937 cells (ATCC CRL1593.2)
Organism Homo sapiens
Characteristics tissue: Pleura/pleural effusion, lymphocyte, myeloid, monocyte
altered gravity condition: microgravity
Treatment protocol Human U937 cells were exposed to altered gravity conditions during a sounding rocket flight.
Growth protocol U937 cells were cultured in RPMI 1640 medium (Biochrom/MerckMillipore, Germany), supplemented with 10% fetal bovine serum (FBS Superior; Biochrom/Merck Millipore, Germany), 2mM glutamine (Gibco/Life Technologies, Germany), and 100U/mL penicillin as well as 100 ug/mL streptomycin (Gibco/Life Technologies, Germany). Cells were seeded with a density of 0.2 × 10e6 cells/mL and the medium was exchanged every 48 hours. number.
Extracted molecule total RNA
Extraction protocol Total RNA was extracted using the RNeasy Midi and Maxi kit (Qiagen, Germany). The RNA quality and concentration integrity was measured using an Agilent 2100 Bioanalyzer (Agilent Technologies, USA).
Label Cy3
Label protocol Cy3-labeling with the “Low RNA Input Linear Amplification Kit, PLUS, One-Color” (Agilent Technologies)
 
Hybridization protocol Hybridization for 17.5 h to a NimbleGen expression microarray (12 × 135,000 features) employing the “Gene Expression Hybridization Kit” (Agilent Technologies)
Scan protocol Scanning was performed using the Microarray Scanner G2505B (Agilent Technologies)
Description ug
Data processing The image files of the scanner were analyzed with the NimbleScan Software 2.6 using the robustmultiarray analysis (RMA) with the default parameters. RMA, a probe-level summarization method, identifies probes that are outliers in the overall behavior of the expression measured for a given gene. The contribution of outlier probes is reduced in the reported gene expression level, which has been demonstrated to improve the sensitivity and reproducibility of microarray results. In addition to screening outlier probes, NimbleScan software’s implementation of RMA [Irizarry et al., 2003] used quantile normalization and background correction.( R. A. Irizarry, B.Hobbs, F.Collin et al., “Exploration, normalization, and summaries of high density oligonucleotide array probe level data,” Biostatistics, vol. 4, no. 2, pp. 249–264, 2003)
 
Submission date Jul 12, 2017
Last update date Oct 16, 2018
Contact name Cora S. Thiel
E-mail(s) cora.thiel@uzh.ch
Organization name University of Zurich
Department Institute of Anatomy
Street address Winterthurerstrasse 190
City Zurich
ZIP/Postal code 8057
Country Switzerland
 
Platform ID GPL18943
Series (2)
GSE101299 Dynamic gene expression response to altered gravity in human myelomonocytic U937 cells [sounding rocket]
GSE101309 Dynamic gene expression response to altered gravity in human myelomonocytic U937 cells

Data table header descriptions
ID_REF
VALUE RMA-normalized, averaged gene-level log2 signal intensity

Data table
ID_REF VALUE
AB000409 12.557
AB000463 11.2346
AB000781 6.31396
AB001328 5.97715
AB002294 11.9091
AB002308 11.8924
AB002311 7.22462
AB002313 7.75439
AB002360 5.43915
AB002377 10.8333
AB002381 8.93772
AB002382 8.90969
AB002384 4.32088
AB003177 10.5251
AB003333 10.8858
AB006589 4.15991
AB006590 5.47754
AB006621 4.63907
AB006625 5.34517
AB007457 11.6144

Total number of rows: 45034

Table truncated, full table size 776 Kbytes.




Supplementary file Size Download File type/resource
GSM2700788_513186A06_13-01_Area1_2um_532.pair.gz 2.4 Mb (ftp)(http) PAIR
Processed data included within Sample table

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