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Compared to the medium control, viability was reduced by 47.86% (n = 4, P = 0.0286).
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Cell viability was calculated as percentage of medium control.
While there was no significant reduction in viability detectable immediately after the 24-h incubation with any of the single agents, the combined FluMaf treatment significantly reduced viability of tumour cells and T cells when compared with medium control.
When treated with pK1-5, Hepa129 showed 4.96% less viability than pMock treated cells (n = 4, n.s).. Viability was decreased by 35.37% when compared to the medium control (n = 4, P = 0.0286, Figure 2(a)).
The biochemical, functional, and biological properties were analyzed by the following tests: degradation in saliva medium; controlled drug release; water absorption, mass loss; pH analysis; and biocompatibility through fibroblast cell viability by MTT assay.
From a total of 53 tested breast cancer specimens, three showed a too low ATP content of the culture medium controls after a culture time of 6 days probably owing to a too low viability of the isolated tumour cells.
In control cells, viability was increased 2.8 fold in medium containing 0.5% FCS and HRG compared with medium supplemented with 0.5% FCS only.
Examined by crystal violet staining, 200 nM doxorubicin in MSCM (fresh MSC culture medium) decreased cell viability to 0.58 ± 0.039-fold to control; however, doxorubicin in CM of MSC-ad only decreased cell viability to 0.84 ± 0.036-fold 0.036-fold
Medium access control sublayer.
medium access control.
sensor medium access control.
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