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Initially, aerodynamic imbalances must be detected using optical methods.
Emission was detected using optical filters as follows: (band-pass filters) CFP, 470±20 nm; GFP, 510±30 nm; YFP, 530±25 nm; (long pass filter) orange and red FP variants, 590 LP filter.
The element distribution in the oxide layers of four groups of samples were detected using glow discharge optical emission spectroscopy (GDOES), and oxide layer structures of two representative groups of samples were analyzed using transmission electron microscopy (TEM) techniques.
Fluorescence was detected using an Axio Imager optical sectioning microscope with an ApoTome slider module.
The immunoreactive bands of PG receptors and β-actin were visualized with a BeyoECL plus chemiluminescence detection kit, and the optical density bands were detected using a BioRad gel imaging and analysis system.
The interference fringes are detected using two photodetectors on the input optical bench.
Fluorescence emmision of NBD-cholesterol were detected using the control of an acusto optical tuneable filter (AOTF).
The amplified fragments were detected using Power SYBER Green PCR Master Mix (Applied Biosystems, Life Technologies) in optical 96-well MicroAmp plates using 7300 real-time PCR system (Applied Biosystems).
A reflected optical pulse was detected using a photodetector and converted into an electronically tunable TTL signal as a trigger signal.
Layers of ε-Fe2+x(C,N) of several micrometers were detected using X-ray diffraction and glow discharge optical spectroscopy.
The displacement of reflector can be detected using fiber coupler from the change of optical power light reflected by the reflector.
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