Abstract: A lighting apparatus comprises a controller and three lights sources each with a different color temperature. The controller turns on the second light source and the third light source alternately at a strobing frequency between 30 Hz and 65 Hz, resulting in a strobing light (out of the second light source and the third light source) with a combined color temperature approximating the color temperature of the first light source. Alternatively, the lighting apparatus includes a controller and two light sources. The first light source and the second light source operate at different frequencies, resulting in a superimposed light with an operating frequency equal to the difference of these two frequencies. Alternatively, the lighting apparatus turns off one of the two light sources periodically for a short period of time to induce the brain of a subject to better recognize the frequency of the superimposed light.

Abstract: A self-disinfecting photocatalyst sheet includes a substrate material, a photocatalyst layer, and a primer. The photocatalyst layer comprises a primary photocatalyst and a secondary photocatalyst. The primary photocatalyst is anatase titanium dioxide and the secondary photocatalyst comprises a metallic photocatalyst. The secondary photocatalyst absorbs a visible light energy, transfers the energy to the primary photocatalyst, thus activating the primary photocatalyst as the primary disinfecting agent. The substrate material binds the photocatalyst layer by either connecting the primary photocatalyst and/or the secondary photocatalyst through two oxygen atoms of a carboxyl group (COO) comprising the primer, or by forming hydrogen bonds between the carbonyl group and a surface hydroxyl group (OH—) of the primary photocatalyst. The self-disinfecting photocatalyst sheet is activatable by a visible light and can self-disinfect against bacteria and viruses.

Abstract: A non-contact phase-locked and self-injection-locked vital sign sensor includes a self-oscillating voltage-controlled frequency-adjustable radiating element and a phase-locked loop. The self-oscillating voltage-controlled frequency-adjustable radiating element is used for transmitting an oscillation signal to an organism and for receiving a corresponding reflected signal from the organism to be posed at a self-injection-locked state, the oscillation signal being tuned by a vital sign of the organism to form a frequency-tuned signal. The phase-locked loop is used for demodulating the frequency-tuned signal to obtain a corresponding vital signal of the organism. By comparing the oscillation signal frequency-eliminated and outputted from the self-oscillating voltage-controlled frequency-adjustable radiating element with a reference signal, a corresponding comparison result is used to vary a phase of the frequency-divided oscillation signal for maintaining the same phase of the reference signal.

Abstract: In a noncontact self-injection-locked sensor, a self-injection-locked oscillating integrated antenna is designed to radiate a signal to a subject and be injection-locked by a reflect signal reflected from the subject. Owing to the reflect signal is phase-modulated by vital signs of the subject, a demodulator is provided to demodulate an injection-locked signal of the self-injection-locked oscillating integrated antenna to obtain a vital signal of the subject.

Abstract: A non-contact phase-locked and self-injection-locked vital sign sensor includes a self-oscillating voltage-controlled frequency-adjustable radiating element and a phase-locked loop. The self-oscillating voltage-controlled frequency-adjustable radiating element is used for transmitting an oscillation signal to an organism and for receiving a corresponding reflected signal from the organism to be posed at a self-injection-locked state, the oscillation signal being tuned by a vital sign of the organism to form a frequency-tuned signal. The phase-locked loop is used for demodulating the frequency-tuned signal to obtain a corresponding vital signal of the organism. By comparing the oscillation signal frequency-eliminated and outputted from the self-oscillating voltage-controlled frequency-adjustable radiating element with a reference signal, a corresponding comparison result is used to vary a phase of the frequency-divided oscillation signal for maintaining the same phase of the reference signal.

Abstract: In a noncontact self-injection-locked sensor, a self-injection-locked oscillating integrated antenna is designed to radiate a signal to a subject and be injection-locked by a reflect signal reflected from the subject. Owing to the reflect signal is phase-modulated by vital signs of the subject, a demodulator is provided to demodulate an injection-locked signal of the self-injection-locked oscillating integrated antenna to obtain a vital signal of the subject.

Abstract: This invention discloses systems and methods for determining the sequence of amino acids in a short peptide chain that constructs a protein. The protein is firstly hydrolyzed to various short peptides and amino acid enantiomers. Then, the systems and method are used to separate the short peptides and the amino acid enantiomers, identify qualitatively each of the amino acid enantiomers, and obtain the molecular mass signal for each of the peptides. After that, the identified amino acid enantiomers are used to construct any possible short peptides in an order from the smallest molecular weight dipeptide to higher molecular weight short peptides, and the correct short peptides is confirmed by matching the molecular weight obtained from the mass spectrometry measurement, then, the short peptides are combined to give a large peptide. The process is continued until the whole amino acid sequence of the peptide chain of protein can be determined.

Abstract: This invention discloses systems and methods for determining the sequence of amino acids in a short peptide chain that constructs a protein. The protein is firstly hydrolyzed to various short peptides and amino acid enantiomers. Then, the systems and method are used to separate the short peptides and the amino acid enantiomers, identify qualitatively each of the amino acid enantiomers, and obtain the molecular mass signal for each of the peptides. After that, the identified amino acid enantiomers are used to construct any possible short peptides in an order from the smallest molecular weight dipeptide to higher molecular weight short peptides, and the correct short peptides is confirmed by matching the molecular weight obtained from the mass spectrometry measurement, then, the short peptides are combined to give a large peptide. The process is continued until the whole amino acid sequence of the peptide chain of protein can be determined.