Abstract: A method of analyzing biological particles for a biological particle analyzer includes outputting a first detection result when at least one particle has arrived at the first detection area, outputting a second detection result to the control module when the particles have arrived at the second detection area, and determining when to turn on or off the light emission source and outputting a control signal to turn on or off the light emission source according to the first detection result, wherein a control module is configured to calculate a turn-on time according to different particle characteristics and an average velocity of the at least one particle, and the light emission source is turned on only when the at least one particle is being tested during the turn-on time.

Abstract: The present invention discloses a guiding device for guiding a dispenser to draw solution from at least one well on a microplate. The guiding device includes a column body whereon a first opening and a second opening are formed on opposite sides, and a slotting structure passing through the column body and communicating with the first opening and the second opening. A pipe of the dispenser passes through the first opening, the slotting structure and the second opening to reach inside the at least one well on the microplate for drawing the solution contained in the at least one well.

Abstract: A method of analyzing biological particles for a biological particle analyzer includes outputting a first detection result when at least one particle has arrived at the first detection area, outputting a second detection result to the control module when the particles have arrived at the second detection area, and determining when to turn on or off the light emission source and outputting a control signal to turn on or off the light emission source according to the first detection result, wherein a control module is configured to calculate a turn-on time according to different particle characteristics and an average velocity of the at least one particle, and the light emission source is turned on only when the at least one particle is being tested during the turn-on time.

Abstract: A biological particle analyzer is disclosed and includes a microchannel including an end coupled to a first drive electrode, another end coupled to a second drive electrode, a first detection area at an upstream location and an excitation area at a downstream location for containing particles flowing from the upstream location to the downstream location inside the microchannel, a first detection circuit coupled to the first detection area for outputting a first detection result when at least one particle has arrived at the first detection area, a light emission source, and a control module coupled to the first detection circuit and the light emission source for determining when to turn on or off the light emission source according to the first detection result.

Abstract: A measurement device with electroencephalography (EEG) and electrocardiography (ECG) functionalities includes a shell and a turning structure. The shell includes a first contact and a second contact located at a first side of the shell; and a third contact. The turning structure, disposed on the shell, is utilized for adjusting the third contact to be located at the first side when the measurement device is in an EEG mode, and adjusting the third contact to be located at a second side of the shell when the measurement device is in an ECG mode, wherein the second side is substantially opposite to the first side.

Abstract: A biochip detecting device for detecting a biochip is provided. The biochip receives an incident light to produce an excitation light. Both the incident light and the excitation light include a specific wavelength. The biochip detecting device includes a light source producing the incident light, an optical attenuator, a filter, a sensor, and a control module electrically connected to the light source and the sensor. Light with the specific wavelength passes through the filter. The optical attenuator disposed between the light source and the filter attenuates an intensity of the incident light, and replaces the biochip. The sensor detects an intensity of the light with the specific wavelength attenuated by the optical attenuator, and generates an intensity signal. The control module adjusts the intensity of the incident light according to whether the intensity signal is complied with a predetermined requirement. A detection method for the light source is provided.

Abstract: A measurement device with electroencephalography (EEG) and electrocardiography (ECG) functionalities includes a shell and a turning structure. The shell includes a first contact and a second contact located at a first side of the shell; and a third contact. The turning structure, disposed on the shell, is utilized for adjusting the third contact to be located at the first side when the measurement device is in an EEG mode, and adjusting the third contact to be located at a second side of the shell when the measurement device is in an ECG mode, wherein the second side is substantially opposite to the first side.

Abstract: A measurement device with electroencephalography (EEG) and electrocardiography (ECG) functionalities includes a shell and a turning structure. The shell includes a first contact and a second contact located at a first side of the shell; and a third contact. The turning structure, disposed on the shell, is utilized for adjusting the third contact to be located at the first side when the measurement device is in an EEG mode, and adjusting the third contact to be located at a second side of the shell when the measurement device his in an ECG mode, wherein the second side is substantially opposite to the first side.

Abstract: A measurement device with electroencephalography (EEG) and electrocardiography (ECG) functionalities includes a first shell having ECG functionality and a second shell. The first shell includes a first contact and a second contact located at a first side of the first shell; and a third contact located at a second side of the first shell, wherein the second side of the first shell is substantially opposite to the first side of the first shell. The second shell includes a fixing device, for connecting with and fixing on the first shell; and a fourth contact, a fifth contact and a sixth contact, located at a first side of the second shell, for electrically connecting with the first contact, the second contact and the third contact respectively when the first shell is connected to and fixed on the fixing device, in order to perform EEG measurement.

Abstract: A bio-sensing device includes a first platform, a second platform, at least one first magnetic element, and at least one second magnetic element. The first platform is configured to support a microplate. The microplate has a plurality of wells, each of which stores a reagent and a plurality of microbeads. The second platform is movably placed below the first platform. The first and the second magnetic elements are respectively located on the second platform. The first magnetic element moves along with the second platform to magnetically attract the microbeads in the wells, the second magnetic element moves along with the second platform to demagnetize the microbeads in the wells, and magnetism of the first magnetic element is opposite to magnetism of the second magnetic element.

Abstract: A measurement device with electroencephalography (EEG) and electrocardiography (ECG) functionalities includes a first shell having ECG functionality and a second shell. The first shell includes a first contact and a second contact located at a first side of the first shell; and a third contact located at a second side of the first shell, wherein the second side of the first shell is substantially opposite to the first side of the first shell. The second shell includes a fixing device, for connecting with and fixing on the first shell; and a fourth contact, a fifth contact and a sixth contact, located at a first side of the second shell, for electrically connecting with the first contact, the second contact and the third contact respectively when the first shell is connected to and fixed on the fixing device, in order to perform EEG measurement.

Abstract: A measurement device with electroencephalography (EEG) and electrocardiography (ECG) functionalities includes a shell and a turning structure. The shell includes a first contact and a second contact located at a first side of the shell; and a third contact. The turning structure, disposed on the shell, is utilized for adjusting the third contact to be located at the first side when the measurement device is in an EEG mode, and adjusting the third contact to be located at a second side of the shell when the measurement device his in an ECG mode, wherein the second side is substantially opposite to the first side.

Abstract: The present invention discloses a guiding device for guiding a dispenser to draw solution from at least one well on a microplate. The guiding device includes a column body whereon a first opening and a second opening are formed on opposite sides, and a slotting structure passing through the column body and communicating with the first opening and the second opening. A pipe of the dispenser passes through the first opening, the slotting structure and the second opening to reach inside the at least one well on the microplate for drawing the solution contained in the at least one well.

Abstract: A bio-sensing device includes a first platform, a second platform, at least one first magnetic element, and at least one second magnetic element. The first platform is configured to support a microplate. The microplate has a plurality of wells, each of which stores a reagent and a plurality of microbeads. The second platform is movably placed below the first platform. The first and the second magnetic elements are respectively located on the second platform. The first magnetic element moves along with the second platform to magnetically attract the microbeads in the wells, the second magnetic element moves along with the second platform to demagnetize the microbeads in the wells, and magnetism of the first magnetic element is opposite to magnetism of the second magnetic element.

Abstract: The present invention discloses a biochip measuring system. The cytometer system includes a biochip and a biochip measuring apparatus. The biochip includes a substrate, for carrying bio-molecule droplet, and a stamp marking area, for receiving or displaying a stamp for identifying whether the biochip is used. The biochip measuring apparatus includes a controller, a driver circuit, a driver interface, a light, a light detector, and a stamp marking unit, for marking the stamp on the stamp marking area of the biochip after the biochip measuring apparatus completes measurement of the biochip.

Abstract: A biochip detecting device for detecting a biochip is provided. The biochip receives an incident light to produce an excitation light. Both the incident light and the excitation light include a specific wavelength. The biochip detecting device includes a light source producing the incident light, an optical attenuator, a filter, a sensor, and a control module electrically connected to the light source and the sensor. Light with the specific wavelength passes through the filter. The optical attenuator disposed between the light source and the filter attenuates an intensity of the incident light, and replaces the biochip. The sensor detects an intensity of the light with the specific wavelength attenuated by the optical attenuator, and generates an intensity signal. The control module adjusts the intensity of the incident light according to whether the intensity signal is complied with a predetermined requirement. A detection method for the light source is provided.

Abstract: A biological particle analyzer is disclosed and includes a microchannel including an end coupled to a first drive electrode, another end coupled to a second drive electrode, a first detection area at an upstream location and an excitation area at a downstream location for containing particles flowing from the upstream location to the downstream location inside the microchannel, a first detection circuit coupled to the first detection area for outputting a first detection result when at least one particle has arrived at the first detection area, a light emission source, and a control module coupled to the first detection circuit and the light emission source for determining when to turn on or off the light emission source according to the first detection result.

Abstract: The present invention discloses a biochip measuring system. The cytometer system includes a biochip and a biochip measuring apparatus. The biochip includes a substrate, for carrying bio-molecule droplet, and a stamp marking area, for receiving or displaying a stamp for identifying whether the biochip is used. The biochip measuring apparatus includes a controller, a driver circuit, a driver interface, a light, a light detector, and a stamp marking unit, for marking the stamp on the stamp marking area of the biochip after the biochip measuring apparatus completes measurement of the biochip.

Abstract: A test system, a test signal auxiliary device, and a test signal generation method thereof are disclosed. The test signal auxiliary device is used for providing a computer system to test a signal measurement device. The test signal auxiliary device includes a first signal input terminal used for receiving an analog test signal via a first audio port of the computer system. A filter module is used for filtering the analog test signal to produce a filtered signal. A first signal output terminal is used for outputting the filtered signal to the signal measurement device. A second signal input terminal is used for receiving a corresponding signal from the signal measurement device. A second signal output terminal is used for transmitting the corresponding signal to the computer system via a second audio port.