Sentence examples for excitation setting from inspiring English sources

Cary Eclipse fluorescent spectrophotometer uses pulsed xenon lamp (80 Hz; 2 μs pulse width at half peak height) for luminescence excitation, setting the intensity measured before each pulse (thus, in about 12.5 ms after previous pulse) as zero for the background correction.

All images were obtained with a ×40 oil immersion lens under the 488-nm excitation setting.

In the elliptic RF excitation setting, the amplitude voltage of one transmit channel was automatically reduced by the scanner by approximately 54% in relation to that of the second channel.

With the short-wavelength detection setting of 490 530 nm, and a laser excitation setting of 561 nm, a bright neuron against a dark and low noise background emerged.

In all three settings samples were read in the Floustar Galaxy fluorometer with excitation set at 405 nm and emission read at 615 nm with a 400  μs delay and a 400  μs acquisition window.

The fluorescence was measured for 2 h with the excitation set to 460 nm and the emission recorded at 520 nm at 2 min intervals at 37°C.

After 30 min incubation, fluorescence was detected using a Synergy HT microplate reader (BIO-TEK) with excitation set at 490 nm and emission detected at 520 nm.

Fluorescence was quantified in a microplate reader (TECAN Infinite M200) with excitation set at 410 nm (9 nm bandwidth) and emission at 450 nm for blue fluorescence and 520 nm for green fluorescence (20 nm bandwidth).

Cells were analyzed in Epic Profile flow cytometer, with excitation set at 488 nm.

The fluorescence intensity was measured immediately using a fluorometer (LS50B; Perkin-Elmer, Waltham, MA, USA), with excitation set at 495 nm and emission set at 520 nm.

The derivatized glutathione was detected by a Waters ACQUITY UPLC® fluorescence detector with the excitation set to 390 nm and the emission set to 480 nm.