Sentence examples for detection at the end from inspiring English sources

Real-time PCR reactions were carried out using the Eppendorf Realplex thermocycler with the following conditions: 95°C for 10 min., 40 repeated cycles including denature (95°C), annealing (60°C), and extension (72°C) with fluorescence detection at the end of each 72°C step, and then melted with continuous fluorescence detection to 95°C.

All of the 106 patients underwent MRD detection at the end of induction of CR and one cycle of consolidation.

Determining the correct end points of segments is a known difficulty while identifying segments, and IBD detection at the end of chromosomes is lower.

Amperometric detection at the end of the column employed a glassy carbon thin layer radial cell (Bioanalytical Systems, West Lafayette, IN) held at +0.8 V relative to a Ag/AgCl reference.

The PCR conditions were as follows: 1 cycle of 95 °C for 10 min and 40 cycles of 95 °C for 10 s and 60 °C for 60 s, with real-time detection at the end of each cycle.

On the other hand, Ph. chrysosporium and the two Pleurotus spp. were early MnP producers since their maximum production (0.4 3.0 U L−1) was noted within the first 12 days of growth, and then it gradually subsided to levels of no detection at the end of cultivation.

Single point detections at the end point of fibril formation do not provide detailed information about the effect of additives to the amyloid fibril formation process.

Each probe pair consisted of a common probe with a phosphate modification at the 5′ end and a unique sequence (complementary zipcode) at the 3′ end and a discriminating probe with the specific nucleotide at the 3′ end and a label for detection at the 5′ end.

Electrophoretic mobility shift analysis of ATP-dependent disruption of Mot1 TBP DNA complexes with and without NC2 as in Figure 2, but using DNA substrates that carry a digoxygenin label at one end (circle) and fluorescein for DNA detection at the other end (star).

Argon laser-induced fluorescence (LIF) detector was used to monitor simultaneously the SPE reservoir and the detection site at the end of the electrophoresis channel.

The conditions of amplification consisted of an initial denaturation step at 95°C for 5 min as a "hot start" followed by 40 cycles at 95°C for 30 s/60°C for 30 s with a single fluorescence detection point at the end of the relevant annealing or extension segment.