Abstract: A plant-based functional polyester filament and a preparation method of the plant-based functional polyester filament are provided. The plant-based functional polyester filament includes polyester, and plant extract in a weight percentage range of approximately 0.1%-1.5%. The plant extract includes one or more of a peppermint extract, a valerian extract, a lavender extract, a wormwood extract, a chitin extract and a seaweed extract. The method includes preparing a plant-based functional polyester masterbatch, including: heating polyethylene terephthalate (PET) chips to a molten state, adding an antioxidant and a dispersant to the molten PET, stirring the molten PET, adding a protective agent and a plant extract to the molten PET, stirring the molten PET at a high speed, adding a modifier to the molten PET, obtaining a mixture by uniformly mixing the molten PET, and performing an extrusion granulation process on the mixture.

Abstract: A method for processing textile fibers is provided. The method comprises: adding a plurality of raw materials for processing textile fibers into a plurality of kettles; preparing supercritical carbon dioxide; obtaining one or more natural plant dyes and one or more natural plant extracts from the plurality of raw materials, and dissolving the one or more natural plant dyes and the one or more natural plant extracts in the supercritical carbon dioxide; dyeing and functionally modifying the textile fibers simultaneously by using the supercritical carbon dioxide carrying a mixture of the one or more natural plant dyes and the one or more natural plant extracts; performing a post-process to recycle the supercritical carbon dioxide; and performing a cleaning process to clean the one or more natural plant dyes and one or more natural plant extracts.

Abstract: A plant-based functional polypropylene spunbond non-woven fabric and a preparation method of the plant-based functional polypropylene spunbond non-woven fabric are provided. The plant-based functional polypropylene spunbond non-woven fabric contains a plant herb water-soluble extract in a weight percentage range of approximately 0.2%-1.5%. The plant-based functional polypropylene spunbond non-woven fabric has moisture regain in a range of approximately 0.2%-3%, a longitudinal breaking strength of approximately ?18.5 N/5 cm, a transverse breaking strength of approximately ?9.5 N/5 cm, a thickness in a range of approximately 0.2 mm-0.5 mm, a weight per unit area in a range of approximately 20 g/m2-40 g/m2, and a fiber diameter in a range of approximately 10 ?m-30 ?m.

Abstract: The present invention discloses an algae modified pp spunbond non-woven fabric, which contains 0.1-2% of alginate. The algae modified pp spunbond non-woven fabric has a moisture regain of 0.2-3.5%, and an antibacterial rate ?98%. The algae modified pp spunbond non-woven fabric prepared in the invention contains modified alginic acid, and also has hydrophilic functional groups, such as hydroxyl and amido groups, and hydrophobic functional groups such as branched alkyl groups.

Abstract: A plant-extract-containing polyester fiber is provided. The plant-extract-containing polyester fiber comprises raw materials including polyester chips, calcium carbide powder, cycloalkyl powder, halloysite powder, plant-extract functional additive, allyl glycidyl ether, organic acid salt, chromium sulfate, dispersing agent, surface active phospholipid, plasticized starch, chitosan, wetting agent, sodium salt of caboxy methyl cellulose, and antistatic agent.

Abstract: Methods and devices for accurate genome sequencing, including sequencing of single cells by single-stranded amplification and sequencing are provided herein.

Abstract: The present disclosure features compositions and methods related to the detection and molecular profiling of extracellular vesicles using fluorescent probes. These compositions and methods leverage the unique optoelectrical properties of quantum dots and fluorescently labeled nanoparticles, which allows reliable, real-time detection of extracellular vesicles and vesicle surface bound or lumenal molecules.

Abstract: Provided herein are methods and devices for accurate sequencing and detection of epigenetic information from template polynucleotides. Also provided are methods for long-range strand displacement amplification of polynucleotides, microfluidic devices with selectively permeable barriers for multistep processing, and methods for polynucleotide amplification using the microfluidic devices.

Abstract: The present invention discloses a light-emitting diode (LED) lamp and an installation method for the LED lamp. The LED lamp includes: a lamp holder and a lampshade installed on the lamp holder. A printed circuit board (PCB) is disposed between the lamp holder and the lampshade. The PCB is provided with a light source component. The lampshade is integrally formed. By means of modular design for each element of the LED lamp, installation of the LED lamp is convenient. After modular design, each module of the LED lamp can be directly used for separate sale, thereby realizing modular after-sales services.

Abstract: A method for processing textile fibers is provided. The method comprises: adding a plurality of raw materials for processing textile fibers into a plurality of kettles; preparing supercritical carbon dioxide; obtaining one or more natural plant dyes and one or more natural plant extracts from the plurality of raw materials, and dissolving the one or more natural plant dyes and the one or more natural plant extracts in the supercritical carbon dioxide; dyeing and functionally modifying the textile fibers simultaneously by using the supercritical carbon dioxide carrying a mixture of the one or more natural plant dyes and the one or more natural plant extracts; performing a post-process to recycle the supercritical carbon dioxide; and performing a cleaning process to clean the one or more natural plant dyes and one or more natural plant extracts.

Abstract: Magnetic-optical iron oxide-gold core-shell nanoparticles are disclosed. Methods for making and using the nanoparticles are also disclosed.

Abstract: Provided herein are methods and devices for accurate sequencing and detection of epigenetic information from template polynucleotides. Also provided are methods for long-range strand displacement amplification of polynucleotides, microfluidic devices with selectively permeable barriers for multistep processing, and methods for polynucleotide amplification using the microfluidic devices.

Abstract: The invention provides improved methods for sequencing nucleic acids, e.g., for medical applications and biomedical research. The disclosed methods can be applied to rapid personalized medicine, genetic diagnosis, pathogen identification, and sequencing species genomes.

Abstract: The present invention provides a compound of the Formula I, or a pharmaceutically acceptable salt, solvate or ester thereof, wherein R, R1, R2, R3, m and are as defined herein. The compounds are ERK inhibitors. Also disclosed are pharmaceutical compositions that comprise the above compounds, and methods of treating cancer using the same.

Abstract: The present invention relates to novel Anilinopiperazine Derivatives of Formula (I), compositions comprising the Anilinopiperazine Derivatives, and methods for using the Anilinopiperazine Derivatives for treating or preventing a proliferative disorder, cancer, an anti-proliferative disorder, inflammation, arthritis, a central nervous system disorder, a cardiovascular disease, alopecia, a neuronal disease, an ischemic injury, a viral disease, a fungal infection, or a disorder related to the activity of a protein kinase.

Abstract: Methods and devices for accurate genome sequencing, including sequencing of single cells by single-stranded amplification and sequencing are provided herein.

Abstract: Provided herein are methods of assembling high density biomolecular arrays. The disclosed methods and devices combine a photolithographic step with the assembly of particles conjugated to biomolecules. The methods provided herein are particularly useful for the assembly of large, high density biomolecular arrays like protein arrays for chip-based assays and DNA arrays for genomic analysis.

Abstract: The present invention provides a compound of the Formula I: (Formular I should be inserted here) or a pharmaceutically acceptable salt, solvate or ester thereof, wherein R, R1, R2 and R3 are as defined herein. The compounds are ERK inhibitors. Also disclosed are pharmaceutical compositions comprising the above compounds and methods of treating cancer using the same.

Abstract: Magnetic-optical iron oxide-gold core-shell nanoparticles are disclosed. Methods for making and using the nanoparticles are also disclosed.

Abstract: In this invention a hit ahead multi-level hierarchical scalable priority encoding logic and circuits are disclosed. The advantage of hierarchical priority encoding is to improve the speed and simplify the circuit implementation and make circuit design flexible and scalable. To reduce the time of waiting for previous level priority encoding result, hit signal is generated first in each level to participate next level priority encoding, and it is called Hit Ahead Priority Encoding (HAPE) encoding. The hierarchical priority encoding can be applied to the scalable architecture among the different sub-blocks and can also be applied with in one sub-block. The priority encoding and hit are processed completely parallel without correlation, and the priority encoding, hit generation, address encoding and MUX selection of the address to next level all share same structure of circuits.