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For cytogenetic and microarray testing, the most recent International System for Human Cytogenetic Nomenclature (ISCN) nomenclature should be used.
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Using a mutant screen strategy, we studied the role of some altered genes (up- or down-regulated in the microarrays) by testing the survival of available corresponding P-element or UAS construct lines under hyperoxic conditions.
There are over 2500 genes known in the donor region for the congenic strain, so as in previous examples, after QTL mapping, microarray testing was the single step that reduced the number of candidate genes the most.
In order to evaluate the reliability of the miRNA microarray, we tested the reproducibility of the data from multiple hybridizations.
To validate the differential expression observed by DNA microarray, we tested the expression of 13 markers encoding known proteins by real-time Q-PCR.
We use our 1344-feature 'synovial proteome' antigen microarrays to test the hypothesis that microarray-based specific detection of autoantibodies against candidate antigens enables diagnosis and classification of RA.
FAC carried out the microarray testing and performed the statistical analysis.
We have designed resequencing microarrays to test the performance of this platform when interrogating a large number of exons (164 total) from genes associated with cancer.
We ran cDNA microarrays to test the array of genes related to angio-genesis that were affected by hUCBSC treatment.
We next performed immunohistochemistry on tissue microarrays to test the expression of RRBP1 protein across normal breast epithelium, benign hyperplasias, in situ carcinomas, invasive tumors and also metastatic breast cancers.
The combined use of the developed microarray test and the TB-Biochip (MDR) allows the simultaneous identification of the MDR and XDR causative agents and the detection of their resistance profiles in a single day.
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