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As far as we are aware, these issues have never been directly addressed in a single investigation, involving samples of the same polymer system, in complementary experiments expressly designed for these purposes.
In complementary experiments, we also determined whether a specific downregulation of Gfi1 in wildtype B cells would affect in vitro B cell differentiation.
In complementary experiments, Western blots were prepared using control tissue obtained from an adult rat-brain microsomal preparation or the total lysate from the SVZ eNPC (Figure 2 C).
The effect of carnitine on the intramuscular glutamate and GSH levels was examined in complementary experiments with tumour-bearing mice.
In complementary experiments we also determined the level of IP3, the product of PIP2 hydrolysis, using a Biotrak assay system.
The ability of miR-101 and 5'-isomiR-101 5'-isomiR-101 5'-isomiR-101toer confirmed in complementary experiments designed to evaluate the presence of RISC membind in toansfecthe biotinylated miRISC1 and 5'-isomiR-101.
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The effect of forage conservation method on ruminal lipid metabolism and microbial ecology was examined in 2 complementary experiments in cows.
Unexpectedly, a common equilibration point was not reached in the complementary experiments starting with the co-solvent in the labeled or in the non-labeled S/EHA latex.
In our complementary experiments, the use of Fe acac 2 or FeCl2 failed to prepare FePt nanocubes.
The effects of forage conservation method on plasma lipids, mammary lipogenesis, and milk fat were examined in 2 complementary experiments.
In additional complementary experiments, Ishikawa cells were infected with ERE and either Ad-d1703 or Ad-IκBα (total MOI = 50) and treated as in (ii).
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