Abstract: The invention discloses an integrated detection method of electromagnetic searching, locating and tracking for subsea cables. After being launched into water, the cable-tracking AUV carries out primary Z-shaped reciprocating sailing to search the electromagnetic signal of the target subsea cable, when the electromagnetic signal reaches a preset threshold value, the AUV executes the cable-tracking detection. In the tracking process, if the target electromagnetic signal intensity is lower than the preset threshold, it is determined that subsea cable tracking is lost. At this time, the secondary Z-shaped cable-researching route planning and tracking are performed based on the lost point. In the process that the AUV autonomously tracks and detects the subsea cable, relative locating between AUV and subsea cable is performed based on the electromagnetic signal radiated by the subsea cable, and autonomous tracking control under the guidance of the electromagnetic locating signal is performed.

Abstract: A wireless charging device includes a plug module, a rack and a wireless charger. The plug module has a top wall, and two opposite side walls connected with two opposite sides of the top wall. A front end of a top surface of the top wall of the plug module is defined as an inclined plane. The rack is mounted on the inclined plane of the plug module. A front end of a bottom surface of the rack is recessed inward to form a lower accommodating groove. The inclined plane is mounted in the lower accommodating groove. A top surface of the rack is recessed downward to form an upper accommodating groove. The wireless charger is mounted in the upper accommodating groove.

Abstract: A vehicle-used bracket includes a base body, a clamping assembly and a buffering element. The base body has a main portion, a peripheral wall extended upward from a periphery of a top surface of the main portion, and a connecting portion fastened to a bottom surface of the base body. A periphery of a bottom surface of the connecting portion extends downward to form a limiting structure. The clamping assembly is mounted to the bottom surface of the connecting portion. The clamping assembly includes a screw, a fastening element and a claw. The claw has a fastening piece. A top surface of the fastening piece is arched towards the connecting portion to form at least one protruding block. The at least one protruding block is limited in the limiting structure. The buffering element is mounted between the connecting portion and the clamping assembly.

Abstract: A wireless charging device includes a plug module, a rack and a wireless charger. The plug module has a top wall, and two opposite side walls connected with two opposite sides of the top wall. A front end of a top surface of the top wall of the plug module is defined as an inclined plane. The rack is mounted on the inclined plane of the plug module. A front end of a bottom surface of the rack is recessed inward to form a lower accommodating groove. The inclined plane is mounted in the lower accommodating groove. A top surface of the rack is recessed downward to form an upper accommodating groove. The wireless charger is mounted in the upper accommodating groove.

Abstract: A wireless charger includes a housing which is a circular plate shape, a wireless charging module and a holder. An inside of the housing has an internal space. A front of a lower portion of a peripheral surface of the housing is recessed inward to form a holding slot. Two sides of the housing define two blind holes. The holding slot is connected with the two blind holes. The wireless charging module is assembled in the internal space. The holder is placed in the holding slot. The holder is pivotally located in the housing. The holder is rotatable around a bottom surface of the housing. The holder has a frame, and two pivot pins protruded towards each other from two ends of the frame. The two pivot pins are assembled to the two blind holes.

Abstract: A vehicle-used bracket includes a base body, a clamping assembly and a buffering element. The base body has a main portion, a peripheral wall extended upward from a periphery of a top surface of the main portion, and a connecting portion fastened to a bottom surface of the base body. A periphery of a bottom surface of the connecting portion extends downward to form a limiting structure. The clamping assembly is mounted to the bottom surface of the connecting portion. The clamping assembly includes a screw, a fastening element and a claw. The claw has a fastening piece. A top surface of the fastening piece is arched towards the connecting portion to form at least one protruding block. The at least one protruding block is limited in the limiting structure. The buffering element is mounted between the connecting portion and the clamping assembly.

Abstract: A method of modulation of synthesis capacity on and cleavage properties of synthetic oligomers from solid support is described. The method utilizes linker molecules attached to a solid surface and co-coupling agents that have similar reactivities to the coupling compounds with the surface functional groups. The preferred linker molecules provide an increased density of polymers and more resistance to cleavage from the support surface. The method is particularly useful for synthesis of oligonucleotides, oligonucleotides microarrays, peptides, and peptide microarrays. The stable linkers are also coupled to anchor molecules for synthesis of DNA oligonucleotides using on support purification, eliminating time-consuming chromatography and metal cation presence. Oligonucleotides thus obtained can be directly used for mass analysis, DNA amplification and ligation, hybridization, and many other applications.

Abstract: A wireless power charger includes a shell, a circuit board, a displacement adjusting device and transmitter coils disposed in the shell. The circuit board has a position detection controller for detecting a position of a charging target placed on the shell. A rack is mounted to the displacement adjusting device for only horizontally rotating along with the displacement adjusting device, or horizontally rotating along with the displacement adjusting device and further sliding linearly along a radial direction. The transmitter coils are positioned on the rack. In use, the displacement adjusting device is controlled by the position detection controller to only horizontally rotate the rack, or horizontally rotate the rack and further linearly slide the rack, so as to bring the transmitter coils closer to a receiver coil of the charging target and realize inductive coupling therebetween for charging the charging target.

Abstract: A charger includes a charging body having a base body, two insertion pins apart assembled to a front end of the base body, and at least one USB port equipped in a rear end of the base body. A power plug includes a plug part, a socket part mounted to the plug part and defining two inserting slots, and two electrical terminals located between the socket part and the plug part and each having a pair of contact portions. The plug part has a group of power pins of which one end electrically connects with the electrical terminals and the other end projects outward for plugging in a wall socket. The power plug can be removably attached to the charging body by means of plugging the insertion pins into the corresponding inserting slots to electrically clamp the insertion pin between the contact portions of the corresponding electrical terminal respectively.

Abstract: A method of modulation of synthesis capacity on and cleavage properties of synthetic oligomers from solid support is described. The method utilizes linker molecules attached to a solid surface and co-coupling agents that have similar reactivities to the coupling compounds with the surface functional groups. The preferred linker molecules provide an increased density of polymers and more resistance to cleavage from the support surface. The method is particularly useful for synthesis of oligonucleotides, oligonucleotides microarrays, peptides, and peptide microarrays. The stable linkers are also coupled to anchor molecules for synthesis of DNA oligonucleotides using on support purification, eliminating time-consuming chromatography and metal cation presence. Oligonucleotides thus obtained can be directly used for mass analysis, DNA amplification and ligation, hybridization, and many other applications.

Abstract: A method of modulation of synthesis capacity on and cleavage properties of synthetic oligomers from solid support is described. The method utilizes linker molecules attached to a solid surface and co-coupling agents that have similar reactivities to the coupling compounds with the surface functional groups. The preferred linker molecules provide an increased density of polymers and more resistance to cleavage from the support surface. The method is particularly useful for synthesis of oligonucleotides, oligonucleotides microarrays, peptides, and peptide microarrays. The stable linkers are also coupled to anchor molecules for synthesis of DNA oligonucleotides using on support purification, eliminating time-consuming chromatography and metal cation presence. Oligonucleotides thus obtained can be directly used for mass analysis, DNA amplification and ligation, hybridization, and many other applications.

Abstract: The invention generally relates to spectrometers and optical systems useful therein. More particularly, the invention generally relates to optical systems and systems having improved functionalities, flexibilities, and design options. For example, optical systems of the invention employ an aberration-corrected concave grating along with one or more transmissive aberration correctors.

Abstract: A method of modulation of synthesis capacity on and cleavage properties of synthetic oligomers from solid support is described. The method utilizes linker molecules attached to a solid surface and co-coupling agents that have similar reactivities to the coupling compounds with the surface functional groups. The preferred linker molecules provide an increased density of polymers and more resistance to cleavage from the support surface. The method is particularly useful for synthesis of oligonucleotides, oligonucleotides microarrays, peptides, and peptide microarrays. The stable linkers are also coupled to anchor molecules for synthesis of DNA oligonucleotides using on support purification, eliminating time-consuming chromatography and metal cation presence. Oligonucleotides thus obtained can be directly used for mass analysis, DNA amplification and ligation, hybridization, and many other applications.

Abstract: A method of modulation of synthesis capacity on and cleavage properties of synthetic oligomers from solid support is described. The method utilizes linker molecules attached to a solid surface and co-coupling agents that have similar reactivities to the coupling compounds with the surface functional groups. The preferred linker molecules provide an increased density of polymers and more resistance to cleavage from the support surface. The method is particularly useful for synthesis of oligonucleotides, oligonucleotides microarrays, peptides, and peptide microarrays. The stable linkers are also coupled to anchor molecules for synthesis of DNA oligonucleotides using on support purification, eliminating time-consuming chromatography and metal cation presence. Oligonucleotides thus obtained can be directly used for mass analysis, DNA amplification and ligation, hybridization, and many other applications.

Abstract: A method of modulation of synthesis capacity on and cleavage properties of synthetic oligomers from solid support is described. The method utilizes linker molecules attached to a solid surface and co-coupling agents that have similar reactivities to the coupling compounds with the surface functional groups. The preferred linker molecules provide an increased density of polymers and more resistance to cleavage from the support surface. The method is particularly useful for synthesis of oligonucleotides, oligonucleotides microarrays, peptides, and peptide microarrays. The stable linkers are also coupled to anchor molecules for synthesis of DNA oligonucleotides using on support purification, eliminating time-consuming chromatography and metal cation presence. Oligonucleotides thus obtained can be directly used for mass analysis, DNA amplification and ligation, hybridization, and many other applications.

Abstract: The invention generally relates to spectrometers and optical systems useful therein. More particularly, the invention generally relates to optical systems and systems having improved functionalities, flexibilities, and design options. For example, optical systems of the invention employ an aberration-corrected concave grating along with one or more transmissive aberration correctors.

Abstract: A method of modulation of synthesis capacity on and cleavage properties of synthetic oligomers from solid support is described. The method utilizes linker molecules attached to a solid surface and co-coupling agents that have similar reactivities to the coupling compounds with the surface functional groups. The preferred linker molecules provide an increased density of polymers and more resistance to cleavage from the support surface. The method is particularly useful for synthesis of oligonucleotides, oligonucleotides microarrays, peptides, and peptide microarrays. The stable linkers are also coupled to anchor molecules for synthesis of DNA oligonucleotides using on support purification, eliminating time-consuming chromatography and metal cation presence. Oligonucleotides thus obtained can be directly used for mass analysis, DNA amplification and ligation, hybridization, and many other applications.

Abstract: A method of modulation of synthesis capacity on and cleavage properties of synthetic oligomers from solid support is described. The method utilizes linker molecules attached to a solid surface and co-coupling agents that have similar reactivities to the coupling compounds with the surface functional groups. The preferred linker molecules provide an increased density of polymers and more resistance to cleavage from the support surface. The method is particularly useful for synthesis of oligonucleotides, oligonucleotides microarrays, peptides, and peptide microarrays. The stable linkers are also coupled to anchor molecules for synthesis of DNA oligonucleotides using on support purification, eliminating time-consuming chromatography and metal cation presence. Oligonucleotides thus obtained can be directly used for mass analysis, DNA amplification and ligation, hybridization, and many other applications.