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The coefficient of variation of the terminal restriction fragment length assay in the study was 1.5%.
The realisation that most chemotherapeutic agents exert their cytotoxic effects through apoptosis (Reed, 1999) supports the use of cell-death assay in the study of topotecan's antitumour activity in human neoplasms.
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The turn-around time of the assay in this study, including the time for analysis was under 8 hours for the first 12 samples.
Also, Propionibacterium acnes was not included in the pathogen panel of the PCR assay in this study, thus reducing the yield in the delayed-PJI group.
To further evaluate the potential utility of lymphocyte beta adrenergic receptor assays in the study of receptor alterations in human disease, we studied highly purified populations of B and T lymphocytes in peripheral blood to see if differences existed in the concentration or affinity of beta adrenergic receptors and catecholamine-responsive cAMP levels.
Anti-immunoglobulins from other providers were not assayed in the study.
Groups of orthologous sequences assayed in the study.
Western blot analysis to show specificity of antibodies used for ChIP assays in the study.
The four plant extracts used in this study demonstrates good to moderate bioactivities as confirmed by different assays in the study.
Unless otherwise stated, all growth assays in the study were done in replicates of three or five and repeated at least once to confirm the activity.
We then determined whether our 'Wnt signature' genes had been detected as possible targets of TCF4/beta-catenin binding using chromatin immunoprecipitation assays in the study of Hatzis et al. (23).
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