Sentence examples for mixtures were loaded from inspiring English sources
Sample and assay mixtures were loaded onto a 48.48 Dynamic Array integrated fluidic circuit for standard amplification per manufacturer's instructions (Biomark, Fluidigm).
These powdered mixtures were loaded into the DMA using a novel powder-pocket device, which consisted of folded sheet of stainless steel.
Peptide mixtures were loaded onto a 75 μm × 250 mm Acclaim PepMap RSLC column (Thermo Scientific) and separated using a segmented gradient in 120 min from 3 to 30% solvent B (100% acetonitrile with 0.1% formic acid) at a flow rate of 300 nL/min.
The 40 µl reaction mixture consisted of Genotypic master mix (1×), droplet stabilizer (1×), 2 µl of ThunderBolts set 1 or set 2 primers, and 5.0 ng of ctDNA; the mixtures were loaded on each well of a RainDrop® Source chip for droplet generation using the Source instrument (RainDanceTM Technologies).
Increasing quantities of standard mixtures were loaded into a quartz boat and moistened with 0.5 mL of tetramethylammonium hydroxide (TMAH) solution (25% in methanol).
After 10 min of incubation, all binding reaction mixtures were loaded into the MST-grade glass capillaries (NanoTemper Technologies), and thermophoresis was measured with a NanoTemper Monolith-NT115 system (20% light-emitting diode, 20% IR laser power).
150 μg protein of pooled, mixed samples and in addition 100 μg unlabelled protein mixture were loaded via anodic cup loading onto IPGstrips.
Samples of 200 μL of this mixture were loaded into a preparative reverse phase HPLC column to separate the treated enzyme (PrTX-III: HP-2) from HP-2.
This mixture was loaded onto the column, and the flow-through fraction was collected.
The mixture was loaded to a NucleoSpin RNA Mini spin column and washed twice with DNA wash solution.
Protein separation was done using NuPAGE 4 12% BisTris gels (Thermo Scientific), where 10 μl of each sample mixture was loaded per lane, and run in MOPS buffer (Thermo Scientific).
