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After 3 months, the four cultures that had the highest content of live cells were selected to assay the effect of As on biomass (As tolerance assays).
Four of these cultures, with the highest biomass content, were selected (from heap samples T27, T54, Q18, and Q63; data not shown) to assay the effect of As on biomass.
To assay the effect of glucose on OsSUT2 promoter activity, the seeds were imbibed in hygromycin-containing water for 3 days and the germinated embryos were isolated from transgenic seeds.
Furthermore, in order to study the preliminary mechanism of the compounds with potent inhibitory activity, the RT-PCR experiment was performed to assay the effect of selected compounds on mRNA expression of IL-6.
The aim of the present study was to assay the effect of ten 1,2,4-triazole-ciprofloxacin hybrids on planktonic or biofilm-forming haemophili cells in vitro under stationary conditions on the basis of MICs (minimal inhibitory concentrations) and MBICs (minimal biofilm inhibitory concentrations).
Wild-type fly lines were used to assay the effect of sleep deprivation on energy stores.
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Unfortunately it is currently impractical to assay the effects of each of these in mouse models.
This allows us to assay the effects of tethered regulatory factors expressed as fusions with lactose repressor.
To assay the effects of prior light exposure we used procedures previously applied to studies of invertebrate photoreception [9], [18], [19] and in the mouse [12].
In addition, since follicular cells die by apoptosis at the end of oogenesis, it is not possible to assay the effects of long term absence of PcG proteins as has been done in the wing tissue.
Thus, the lateral hippocampal neurons were used to assay the effects of mutations on EphA3 function in growth cone collapse assay.
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