Abstract: The device (100) comprises a cavity (101) and at least two microporous membranes (102), wherein the microporous membranes (102) are arranged in series in the cavity (101) and divide the cavity (101) into a plurality of chambers (1011); each of the microporous membranes (102) is provided with micropores (103), and two adjacent chambers (1011) are in communication via the micropores (103); and each of the chambers (1011) is provided with an electrode (1012).

Abstract: A method of determining a potentially visible set (PVS) includes: dividing a map area into a plurality of detection point areas, the map area corresponding to a movable range of a virtual object in a virtual environment; replacing a map material of a three-dimensional (3D) object in a detection point area with a single-colored material, color identifiers of single-colored materials corresponding to all of 3D objects included in the virtual environment being different; determining at least one detection point in the detection point area; performing rendering to obtain a cubemap corresponding to the at least one detection point, and determining a target color identifier of a single color appearing on the cubemap; and adding a 3D object corresponding to the target color identifier to a PVS of the detection point area.

Abstract: The device (100) comprises a cavity (101) and at least two microporous membranes (102), wherein the microporous membranes (102) are arranged in series in the cavity (101) and divide the cavity (101) into a plurality of chambers (1011); each of the microporous membranes (102) is provided with micropores (103), and two adjacent chambers (1011) are in communication via the micropores (103); and each of the chambers (1011) is provided with an electrode (1012).

Abstract: A micro-nano particle detection device and method are disclosed. The device includes a sample chamber and at least two measurement chambers, where at least one through hole is formed between each measurement chamber and the sample chamber, each measurement chamber is communicated with the sample chamber only through the through hole, a common electrode is arranged in the sample chamber, a measurement electrode is arranged in each measurement chamber respectively, a first end of the sample chamber is provided with a first liquid driving device, and the common electrode is grounded.

Abstract: A method for measuring the concentration of a micro/nano particle, including: allowing the to-be-measured micro/nano particle to bind with one or more kinds of marker to form a new particle, the new particle having a change in at least one of particle size, charge state, and particle morphology compared with the to-be-measured micro/nano particle or the marker; measuring the particle size, charge state, or particle morphology of the new particle and the to-be-measured micro/nano particle or the marker, and counting the new particle and the to-be-measured micro/nano particle or the marker respectively to obtain their respective count results, and, on the basis of the count results, calculating the concentration of the to-be-measured micro/nano particle bound with the marker. The method of the present application has the advantages of high measurement accuracy, low measurement limit, and stability of chemical reagents.

Abstract: A method for detecting a trace protein in a sample system, comprising: providing a primary antibody-modified immunomagnetic bead and a secondary antibody-modified nanoparticle for a to-be-detected protein; mixing and incubating the primary antibody-modified immunomagnetic bead and the secondary antibody-modified nanoparticle with a sample system containing the to-be-detected protein, so as to form a complex having a double-antibody sandwich structure; and allowing the complex to pass through a micro-nano pore device in the form of a single particle and trigger an electrical pulse signal, analyzing the electrical pulse signal to obtain a charge state or a volume/mass state of the complex, and calculating, according to the charge state or the volume/mass state, the amount of the to-be-detected protein in the sample system.

Abstract: A method of determining a potentially visible set (PVS) includes: dividing a map area into a plurality of detection point areas, the map area corresponding to a movable range of a virtual object in a virtual environment; replacing a map material of a three-dimensional (3D) object in a detection point area with a single-colored material, color identifiers of single-colored materials corresponding to all of 3D objects included in the virtual environment being different; determining at least one detection point in the detection point area; performing rendering to obtain a cubemap corresponding to the at least one detection point, and determining a target color identifier of a single color appearing on the cubemap; and adding a 3D object corresponding to the target color identifier to a PVS of the detection point area.