Abstract: A method for continuously collecting fluorescence data of a microfluidic chip is provided. In the method, an optical path system emits a light perpendicular to the microfluidic chip, such that a center of a light spot formed by the optical path system on the microfluidic chip is located on a circle formed by centers of all reaction cells. The microfluidic chip is rotated around a center of the circle formed by centers of all the reaction cells. Fluorescence signal values are collected by using the optical path system along a rotation direction of the microfluidic chip. The collected fluorescence signal values are processed to obtain effective fluorescence data of all the reaction cells.

Abstract: An optical positioning code disk, device and method for a microfluidic chip are provided. A cross section of an outer contour of the code disk is circular. N light transmissive openings are arranged uniformly around the code disk. The device includes: the code disk, a positioning pin, a rotating shaft, a motor, an internal photoelectric switch and an external photoelectric switch. A positioning surface is provided on the rotating shaft. The motor is fixedly connected with an end of the rotating shaft, and the other end of the rotating shaft passes through a center of the cross section of the code disk. The internal and external photoelectric switches are configured to identify the light transmissive openings on the code disk.

Abstract: A concentration gradient fluorescence calibration sheet has a glass substrate and an inorganic nano fluorescent liquid lattice disposed on a surface of the glass substrate. The inorganic nano fluorescent liquid lattice has a plurality of inorganic nano fluorescent liquid sub-lattices. Inorganic fluorescent mixed liquid droplets of each inorganic nano fluorescent liquid sub-lattice are arranged in A rows×B columns. The solution concentration of the same row of inorganic nano fluorescent liquid droplets in the inorganic nano fluorescent liquid sub-lattices is the same, and the solution concentrations of two adjacent rows of inorganic nano fluorescent liquid droplets change in multiples. The concentration gradient fluorescence calibration sheet for the laser microarray chip scanner is utilized to calibrate a scanner under test and a first row of inorganic nano fluorescent liquid droplets in the inorganic nano fluorescent liquid sub-lattices are taken as index marks.

Abstract: An adaptive measurement and calculation method for luminescence values of a chemiluminescence analyzer is provided. A fixed step length is adopted for continuous multi-point reading to obtain a complete correspondence diagram of detection positions and luminescence values. Two nearest luminescence values on the left and right sides of a maximum value are selected, the nearest luminescence values on both sides are connected to form a straight line, and an intersection of two straight lines is taken as an approximate maximum luminescence value. The measurement and calculation method can adapt to random positions of the detected object, and stably obtain the approximate maximum luminescence value, thus reducing increased complex hardware design and cost to confirm accuracy of the measurement position.

Abstract: A concentration gradient fluorescence calibration sheet has a glass substrate and an inorganic nano fluorescent liquid lattice disposed on a surface of the glass substrate. The inorganic nano fluorescent liquid lattice has a plurality of inorganic nano fluorescent liquid sub-lattices. Inorganic fluorescent mixed liquid droplets of each inorganic nano fluorescent liquid sub-lattice are arranged in A rows×B columns. The solution concentration of the same row of inorganic nano fluorescent liquid droplets in the inorganic nano fluorescent liquid sub-lattices is the same, and the solution concentrations of two adjacent rows of inorganic nano fluorescent liquid droplets change in multiples. The concentration gradient fluorescence calibration sheet for the laser microarray chip scanner is utilized to calibrate a scanner under test and a first row of inorganic nano fluorescent liquid droplets in the inorganic nano fluorescent liquid sub-lattices are taken as index marks.

Abstract: A method for continuously collecting fluorescence data of a microfluidic chip is provided. In the method, an optical path system emits a light perpendicular to the microfluidic chip, such that a center of a light spot formed by the optical path system on the microfluidic chip is located on a circle formed by centers of all reaction cells. The microfluidic chip is rotated around a center of the circle formed by centers of all the reaction cells. Fluorescence signal values are collected by using the optical path system along a rotation direction of the microfluidic chip. The collected fluorescence signal values are processed to obtain effective fluorescence data of all the reaction cells.

Abstract: An optical positioning code disk, device and method for a microfluidic chip are provided. A cross section of an outer contour of the code disk is circular. N light transmissive openings are arranged uniformly around the code disk. The device includes: the code disk, a positioning pin, a rotating shaft, a motor, an internal photoelectric switch and an external photoelectric switch. A positioning surface is provided on the rotating shaft. The motor is fixedly connected with an end of the rotating shaft, and the other end of the rotating shaft passes through a center of the cross section of the code disk. The internal and external photoelectric switches are configured to identify the light transmissive openings on the code disk.

Abstract: A method for labeling target molecules coupled to particles for the detection of the target molecules using a microarray chip, comprises: providing a functionalized microparticle, wherein the microparticle is coated with one or more functional group; providing a modification group on each of the target molecules to be detected to form modified target molecules; contacting the functionalized microparticle with the modified target molecules; coupling a luminophore to the complex between the functionalized microparticle and the modified target molecules, thereby directly or indirectly labeling each modified target molecules with the luminophore. By directly or indirectly labeling the target molecules with the luminophore, the method reduces the cost of fluorescence detection, and avoids PCR inhibition derived from traditional fluorescence labeling molecules.

Abstract: In some aspects, the present disclosure relates to a method for identifying the type of the unit by camera.

Abstract: A method for labeling target molecules coupled to particles for the detection of the target molecules using a microarray chip, comprises: providing a functionalized microparticle, wherein the microparticle is coated with one or more functional group; providing a modification group on each of the target molecules to be detected to form modified target molecules; contacting the functionalized microparticle with the modified target molecules; coupling a luminophore to the complex between the functionalized microparticle and the modified target molecules, thereby directly or indirectly labeling each modified target molecules with the luminophore. By directly or indirectly labeling the target molecules with the luminophore, the method reduces the cost of fluorescence detection, and avoids PCR inhibition derived from traditional fluorescence labeling molecules.

Abstract: In some aspects, the present disclosure provides a biochip detecting device that comprises a first shell (2) connect to a second shell (1), and a rotatable support frame (5) of biochip possessing a detecting zone that holds one or more biochips, and a detector (7).

Abstract: Provided herein are methods, devices, and systems of wireless communication. In one embodiment, a method for wireless communication between a first electronic device and a second electronic device includes: providing information symbols to the first electronic device, transmitting a pairing request from the first electronic device to the second electronic device, obtaining a pairing password by accessing a database, and establishing a wireless communication channel between the first electronic device and the second electronic device. In some embodiments, the information symbols are provided audibly or visually by the second electronic device and include a wireless communication address of the second electronic device. In some embodiments, the pairing password is obtained using the wireless communication address. In some embodiments, the wireless communication channel is obtained using the obtained pairing password.

Abstract: A method for labeling target molecules coupled to particles for the detection of the target molecules using a microarray chip, comprises: providing a functionalized microparticle, wherein the microparticle is coated with one or more functional group; providing a modification group on each of the target molecules to be detected to form modified target molecules; contacting the functionalized microparticle with the modified target molecules; coupling a luminophore to the complex between the functionalized microparticle and the modified target molecules, thereby directly or indirectly labeling each modified target molecules with the luminophore. By directly or indirectly labeling the target molecules with the luminophore, the method reduces the cost of fluorescence detection, and avoids PCR inhibition derived from traditional fluorescence labeling molecules.

Abstract: In some aspects, the present disclosure relates to a method for identifying the type of the unit by camera.

Abstract: In some aspects, the present disclosure relates to a method for identifying the type of the unit by camera.

Abstract: The present disclosure provides a cover sheet for a microarray reaction device. In one aspect, the present cover sheet or device ensures the reaction units/volumes are stable and/or consistent among assay samples and assay runs, allowing samples (e.g., reaction solutions) to be conveniently added and distributed uniformly.

Abstract: The present disclosure relates to a method for camera identification and detection on color features. In some aspects, the method comprises: 1) starting the camera, the image processing unit and the display unit at the beginning of testing; 2) using the camera to capture the color characteristic value; and 3) moving the untested object to the detection area of the camera for it to be detected, wherein the image processing unit extracts the mean color characteristic value from the color pixels of the detection area.

Abstract: A microarray-based assay is provided, which is used for analyzing molecular interactions, including polynucleotides, polypeptides, antibodies, small molecule compounds, peptides and carbohydrates. Such method comprises coupling a target molecule to a particle and then binding to a probe molecule on microarray. In particular, multiplexed genetic analysis of nucleic acid fragments can be implemented. Specific genes, single nucleotide polymorphisms or gene mutations, such as deletions, insertions, and indels, can be identified. Coupled with microarray, the particles, themselves or further modified, facilitate the detection of results with non-expensive devices or even naked eyes. This technology enables the detection and interpretation of molecular interactions in an efficient and cost effective way.

Abstract: In some aspects, the present disclosure provides a biochip detecting device that comprises a first shell (2) connect to a second shell (1), and a rotatable support frame (5) of biochip possessing a detecting zone that holds one or more biochips, and a detector (7).

Abstract: A method for labeling target molecules coupled to particles for the detection of the target molecules using a microarray chip, comprises: providing a functionalized microparticle, wherein the microparticle is coated with one or more functional group; providing a modification group on each of the target molecules to be detected to form modified target molecules; contacting the functionalized microparticle with the modified target molecules; coupling a luminophore to the complex between the functionalized microparticle and the modified target molecules, thereby directly or indirectly labeling each modified target molecules with the luminophore. By directly or indirectly labeling the target molecules with the luminophore, the method reduces the cost of fluorescence detection, and avoids PCR inhibition derived from traditional fluorescence labeling molecules.