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Dressing percentage on slaughter weight base was higher (P<0.01) in supplemented sheep than in the non-supplemented ones.
Blood urea nitrogen (BUN) was significantly higher in supplemented groups.
The transfection mix was removed after 4 8 h, and cells were washed with PBS and cultured in supplemented DMEM.
In vitro drug release was measured in supplemented RPMI-1640 at 37 °C.
The results indicated that the serum concentration of Se increased in supplemented does compared with the control ones.
Drug solutions were prepared from a 10 mM stock solution 100% DMSO (Sigma-Aldrich) in supplemented RPMI 1640 media (final DMSO concentration <0.1% v/v).
Isolated cells were washed and diluted in supplemented PBS.
Complement activity increases with stress while lysozyme activity decreases, but to a lesser extent in supplemented fish.
Hepatocytes were then plated out in supplemented media.
HEK-293T (human embryonic kidney 293T cells) cell lines were maintained in supplemented DMEM medium.
The human myeloid leukemia cell line PLB-985 (DSMZ) was cultured in supplemented RPMI 1640 medium.
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