Abstract: A Streptococcus suis (S. suis) vaccine is provided. For the S. suis vaccine, an antigen is a protein with an amino acid sequence shown in SEQ ID NO: 2. A preparation method of the S. suis vaccine is provided, including the following steps: mixing a white oil and aluminum stearate to obtain a white oil adjuvant; adding poly sorbate 80 to an aqueous solution of the protein with the amino acid sequence shown in SEQ ID NO: 2, and thoroughly mixing to obtain an antigen solution; and mixing the antigen solution with the white oil adjuvant according to a volume ratio of (0.5-1.5):2, and emulsifying to obtain the S. suis vaccine. An animal immunized with the S. suis vaccine of the present disclosure can effectively resist the attack of S. suis serotype 2, 3, and 31, with a vaccine protection rate as high as 100%.

Abstract: A Streptococcus suis (S. suis) vaccine is provided. For the S. suis vaccine, an antigen is a protein with an amino acid sequence shown in SEQ ID NO: 2. A preparation method of the S. suis vaccine is provided, including the following steps: mixing a white oil and aluminum stearate to obtain a white oil adjuvant; adding poly sorbate 80 to an aqueous solution of the protein with the amino acid sequence shown in SEQ ID NO: 2, and thoroughly mixing to obtain an antigen solution; and mixing the antigen solution with the white oil adjuvant according to a volume ratio of (0.5-1.5):2, and emulsifying to obtain the S. suis vaccine. An animal immunized with the S. suis vaccine of the present disclosure can effectively resist the attack of S. suis serotype 2, 3, and 31, with a vaccine protection rate as high as 100%.

Abstract: Trifloxystrobin is used for the prevention and treatment of agricultural pest insects and mites. The trifloxystrobin can be configured as an agriculturally allowable emulsifiable concentrate, aqueous emulsion, aqueous solution, wettable powder, microemulsion, suspension, capsule suspension, or water dispersible granule, wherein the content of the trifloxystrobin in the dosage form is 1-80%. The trifloxystrobin has an outstanding effectiveness of control of agricultural pest insects and mites, and trifloxystrobin is a new compound, and there is no cross-resistance with existing products.

Abstract: Provided are an all-solid-state battery and a preparation method thereof. The all-solid-state battery includes a positive electrode, a negative electrode, and a solid-state electrolyte located between the positive electrode and the negative electrode. The negative electrode includes a first negative electrode and a second negative electrode. The second negative electrode is located on a side of the first negative electrode. The solid-state electrolyte includes a first solid-state electrolyte and a second solid-state electrolyte. The first solid-state electrolyte is located between the positive electrode and the first negative electrode. The second solid-state electrolyte is located between the positive electrode and the second negative electrode. The roughness of the second solid-state electrolyte is greater than the roughness of the first solid-state electrolyte.

Abstract: This application discloses a data processing method performed by a computing device. The method includes: acquiring a search keyword of a user, and determining a plurality of target keywords related to the search keyword. After the plurality of keywords are determined, the search keyword and the plurality of target keywords may further be displayed. When the search keyword and the plurality of target keywords are displayed, the plurality of target keywords are distributed on a periphery of a circle with the search keyword as a center in a dispersed manner to achieve a more convenient and intuitive effect. By using this solution, the plurality of target keywords related to the search keyword can be displayed for the user instead of directly providing the user with search results corresponding to the search keyword, and the user obtains the plurality of target keywords through analysis according to the search results.

Abstract: Provided are an alginate dialdehyde-functionalized material, an alginate dialdehyde-modified material, and preparation methods therefor. Further provided is use of the above materials and methods in the manufacture of antibacterial, antifungal, and antiviral protective products. Raw materials used and the preparation methods are simple, economical, environmentally friendly and easy to scale up, have high inhibitory activity against bacteria, fungi and viruses and have great application potential in the fields of biology, medicine, health, etc.

Abstract: Provided are an all-solid-state battery and a preparation method thereof. The all-solid-state battery includes a positive electrode, a negative electrode, and a solid-state electrolyte located between the positive electrode and the negative electrode. The negative electrode includes a first negative electrode and a second negative electrode. The second negative electrode is located on a side of the first negative electrode. The solid-state electrolyte includes a first solid-state electrolyte and a second solid-state electrolyte. The first solid-state electrolyte is located between the positive electrode and the first negative electrode. The second solid-state electrolyte is located between the positive electrode and the second negative electrode. The roughness of the second solid-state electrolyte is greater than the roughness of the first solid-state electrolyte.

Abstract: A recombinant protein and a vaccine composition for porcine epidemic diarrhea (PED) are provided. The recombinant protein is a fusion protein formed by connecting the truncated segment of S protein (Spike protein) from porcine epidemic diarrhea virus (PEDV) in tandem with the Fc fragment of porcine IgG, and the truncated fragment of S protein is preferably selected from N-terminal domain (NTD) with sialic acid binding activity in S1 subunit of S protein, neutralizing epitope domain (COE) and multiple B-cell epitopes in S2 subunit; the vaccine composition contains recombinant protein and adjuvants. The recombinant protein of the application can produce IgG antibody and neutralizing antibody titers of rather high level after immunizing mice, and the proportions of CD3+CD4+, CD3+CD8+ lymphocytes and the concentrations of IFN-? and IL-4 in lymphocytes are significantly increased.

Abstract: According to aspects of the inventive concepts, provided is a method for erasing information based on a dual-security mechanism. A storage medium feature database, an information erasure feature database, and a firmware system feature database are built to match cases for to-be-erased electronic scrap. An erasure solution and a native system data package are generated based on the matching results. The information is erased and an erasure result is evaluated; and the information is recovered on the erased electronic scrap, and a recovery result is evaluated, to implement comprehensive double security evaluation. The information erasure validity of the electronic scrap is checked based on the evaluation results. If an erasure result is invalid, erasure solutions are corrected online based on the evaluation result, until the erasure result is valid and the electronic scrap with a native system recovered is obtained.

Abstract: The present disclosure relates to the field of pharmacology, and in particular, to a preparation method of high-purity total ginkgo flavonol glycoside. The preparation method of high-purity total ginkgo flavonol glycoside includes: (1) mixing Ginkgo biloba extract powder and a first alkaline solution, subjecting to dissolution and centrifugation to obtain a supernatant; (2) subjecting the supernatant to separation with an acid-polar coupled macroporous resin column and to purification with a polyamide column, to obtain high-purity total ginkgo flavonol glycoside. The purity of the total ginkgo flavonol glycoside prepared by the preparation method of high-purity total ginkgo flavonol glycoside according to the present disclosure is ?90%, and has good clinical application prospects; the preparation process does not require organic reagents such as petroleum ether and ethyl acetate, which is environmentally friendly; the transfer rate of the total flavonol glycoside is high.

Abstract: A device may include a processor configured to collect historical location data for a user equipment (UE) device associated with a user and determine a movement pattern for the user based on the collected historical location data. The processor may be further configured to obtain current location data for the UE device over a time period; determine a mobility score for the user for the time period based on the determined movement pattern and the obtained current location data, wherein the mobility score is associated with the user's movements during the time period with respect to the determined movement pattern for the user; and provide the determined mobility score for the user to another device configured to adjust one or more parameters of a radio access network (RAN) associated with the UE device based on the determined mobility score.

Abstract: The present disclosure provides a ginkgo biloba ketone ester capsule. The present disclosure further provides a method for preparing ginkgo biloba ketone ester capsule and use thereof. The present disclosure provides a ginkgo biloba ketone ester capsule and a preparation method thereof. Through optimized preparation operations and conditions, a high-quality ginkgo biloba ketone ester capsule can be obtained. Compared with the ginkgo biloba ketone ester capsule prepared by traditional methods, the ginkgo biloba ketone ester capsule of the present disclosure has stable quality and a low unqualified rate. The consistency of different batches of ginkgo biloba ketone ester capsules is good. In particular, the ginkgo biloba ketone ester capsule can effectively control ginkgolic acids, preventing the use of high-ginkgolic-acid raw materials in the ginkgo biloba ketone ester capsules, so as to effectively improve the safety of ginkgo biloba ketone ester capsules.

Abstract: A device may include a processor configured to collect historical location data for a user equipment (UE) device associated with a user and determine a movement pattern for the user based on the collected historical location data. The processor may be further configured to obtain current location data for the UE device over a time period; determine a mobility score for the user for the time period based on the determined movement pattern and the obtained current location data, wherein the mobility score is associated with the user's movements during the time period with respect to the determined movement pattern for the user; and provide the determined mobility score for the user to another device configured to adjust one or more parameters of a radio access network (RAN) associated with the UE device based on the determined mobility score.

Abstract: The present disclosure provides a Ginkgo biloba ketone ester bulk drug. The present disclosure further provides a method for preparing Ginkgo biloba ketone ester bulk drug and use thereof. The present disclosure provides a Ginkgo biloba ketone ester and a preparation method thereof. Through optimized preparation operations and conditions, high-quality Ginkgo biloba ketone ester bulk drug can be obtained. Compared with the Ginkgo biloba ketone ester prepared by traditional methods, the Ginkgo biloba ketone ester of the present disclosure has stable quality, low unqualified rate, and good consistency of different batches of bulk drugs.

Abstract: The present disclosure relates to a weakly alkaline peracetic acid solution. The present disclosure provides a weakly alkaline peracetic acid solution, comprising a liquid A agent and a powder B agent, the powder B agent being in an amount of 17-23 g relative to per liter of the liquid A agent, wherein the liquid A agent comprises the following components in percentage by mass: 10-20% of hydrogen peroxide with a concentration of 30%, 1-15% of a stabilizer, 0.1-5% of a metal ion chelating agent, 1-10% of an antioxidant, 0.5-2% of a surfactant, and 53-87.4% of deionized water; and the powder B agent comprises the following components: 5-20% of a stabilizer, 5-20% of a corrosion inhibitor, 1-30% of a pH regulator, and 20-50% of an oxide.

Abstract: The disclosure provides a method and an electronic device for recommending crowdsourced tester and crowdsourced testing. The method comprises: collecting a requirement description of a crowd testing task at a time point in a process of crowd software testing and historical crowd testing reports of each tester to be recommended; obtaining a process context and a resource context of each tester to be recommended; inputting the extracted features into a learning to rank model to obtain an initial ranking list of the recommended testers, and re-ranking the initial ranking list based on diversity contributions of expertise and device to obtain a final ranking list. The disclosure can more accurately recommend testers to take accuracy and diversity of the recommended testers into consideration, so that the testers can be dynamically planned during the crowd testing to improve the bug detection rate, shorten the completion cycle of the crowd testing task.

Abstract: The present disclosure relates to the field of pharmacy, specifically to a method for preparing a high-purity ginkgolide and a use thereof. The method for preparing total ginkgolide includes the following steps: (1) mixing a Ginkgo biloba extract powder with an alkali solution, obtaining a precipitate by dissolving and centrifuging; (2) obtaining a total ginkgolide concentrate through purifying the precipitate by silica gel column and recrystallizing. The preparation method of total ginkgolide provided in the present disclosure can improve the purity of total ginkgolide, and the purity of the prepared total ginkgolide is ?80%, which has good clinical application prospect; and the preparation process does not require complicated multi-step recrystallization step, and the total ginkgolide yield is high.

Abstract: Methods and apparatuses (10) for detecting body-related temperature changes are provided. The method comprises measuring a skin-surface temperature at a first temperature sensor element (12) at a measuring rate (S21) and measuring an ambient temperature at a second temperature sensor element (13) at the measuring rate (S22). The method also comprises calculating a plurality of first change rates for the skin-surface temperature and a plurality of second change rates for the ambient temperature over a time interval (S23). The method further comprises determining, based on the plurality of first change rates and the plurality of second change rates, whether an ambient temperature change rate is faster than a skin-surface temperature change rate by a threshold (S24). The method additionally comprises selecting whether or not to trigger an alarm based on a result of the determining (S25). With the methods and apparatuses (10), the number of false alarms may be significantly reduced.

Abstract: According to aspects of the inventive concepts, provided is a method for erasing information based on a dual-security mechanism. A storage medium feature database, an information erasure feature database, and a firmware system feature database are built to match cases for to-be-erased electronic scrap. An erasure solution and a native system data package are generated based on the matching results. The information is erased and an erasure result is evaluated; and the information is recovered on the erased electronic scrap, and a recovery result is evaluated, to implement comprehensive double security evaluation. The information erasure validity of the electronic scrap is checked based on the evaluation results. If an erasure result is invalid, erasure solutions are corrected online based on the evaluation result, until the erasure result is valid and the electronic scrap with a native system recovered is obtained.

Abstract: The present disclosure relates to the field of pharmacology, and in particular, to a preparation method of high-purity total ginkgo flavonol glycoside. The preparation method of high-purity total ginkgo flavonol glycoside includes: (1) mixing Ginkgo biloba extract powder and a first alkaline solution, subjecting to dissolution and centrifugation to obtain a supernatant; (2) subjecting the supernatant to separation with an acid-polar coupled macroporous resin column and to purification with a polyamide column, to obtain high-purity total ginkgo flavonol glycoside. The purity of the total ginkgo flavonol glycoside prepared by the preparation method of high-purity total ginkgo flavonol glycoside according to the present disclosure is ?90%, and has good clinical application prospects; the preparation process does not require organic reagents such as petroleum ether and ethyl acetate, which is environmentally friendly; the transfer rate of the total flavonol glycoside is high.