Exact(1)
The model is tested on a full drug product formulation mixing consisting of API and multiple excipients.
Similar(7)
Solutions before mixing consisted of 20 40 μM FAD-containing enzyme subunit.
A total of 14 HMA mixes consisting of various types, gradations, and nominal maximum aggregate sizes (NMAS) were selected.
The design mixes consisted of varying amounts of FGD, cement, lime, admixture, and water.
Real time qRT-PCR mixes consisted of 1 μL template cDNA to 19 μL master mix.
Hybridization mixes consisted of 50% (v/v) formamide, 10% (w/v) dextran sulfate, 2× SSC, and 2 5 ng/μl probe.
PCR mixes consisted of 25 μl of 2 × LC480 Probes Master (Roche Diagnostics, Almere, the Netherlands), 0.5 μM of each primer and 0.1 μM of each probe, and 5 μl of extracted DNA.
For both HVR and CytB, reaction mixes consisted of 7.5 μL of GoTaq Green Master Mix (Promega), 0.2 μM of each primer, and 5 10 ng of gDNA, made up to 15 μL with ddH2O.
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