Abstract: Provided are composite articles having a membrane and a porous substrate, where the porous substrate has the membrane disposed thereon. The membrane has two layers, where the first layer has the second layer disposed thereon, and each layer has a plurality of polymer chains with a plurality of silicon-oxygen groups and a plurality of silicon-carbon groups. The first layer has a silicon to oxygen ratio of about 4:1 to about 1:1.25 and a silicon to carbon ratio of about 1:2 to about 1:10, and the second layer has a silicon to oxygen ratio of about 1:1 to about 1:2 and a silicon to carbon ratio of about 2:1 to about 10:1. At least a portion of the polymer chains of the second layer am crosslinked. The composite articles may be used in gas separation methods. Also provided are methods of making the composite articles and devices utilizing the composite articles.

Abstract: The present invention provides highly permeable and porous polybenzimidazole membranes, methods of making them, and their application as a high-performance membrane support for gas separation composite membranes. The polybenzimidazole membranes are bonded to a fabric substrate.

Abstract: Sorbent polymer composites and a solution-casting method of making hydrophobic sorbent polymer composites for CO2 adsorption applications are described. The sorbent polymer composites are comprised of a polymer matrix, a dispersed CO2 sorbent, and an optional filler particle for hydrophobicity modification.

Abstract: A micro-droplet fluorescence detection system, comprising a microfluidic chip (1), an optical path device, and a movement control device for controlling the chip (1) and an optical path device to move, so that the chip (1) moves relative to the optical path device during a fluorescence scanning detection process of micro-droplets in the chip (1), and the micro-droplets inside the chip (1) remains stationary relative to the chip (1). The micro-droplet fluorescence detection system has advantages of avoiding cross contamination due to closed detection, high detection rate, high throughput and high sensitivity.

Abstract: A micro-droplet fluorescence detection system, comprising a microfluidic chip (1), an optical path device, and a movement control device for controlling the chip (1) and an optical path device to move, so that the chip (1) moves relative to the optical path device during a fluorescence scanning detection process of micro-droplets in the chip (1), and the micro-droplets inside the chip (1) remains stationary relative to the chip (1). The micro-droplet fluorescence detection system has advantages of avoiding cross contamination due to closed detection, high detection rate, high throughput and high sensitivity.

Abstract: The present invention discloses an asymmetric PCR amplification method, its special primer and application, aims to provide a simple, effective PCR amplification for preparation of single-stranded product. The asymmetric PCR primer of the invention comprises some PCR primer pairs, in which an unrelated nucleic acids sequence to target sequence to be detected is added onto 5?-terminal of one primer. The asymmetric PCR amplification provided includes the steps: 1) preparative denaturing; 2) repetitiously denaturing, primers annealing, extending cycles as the first stage of PCR amplification; 3) repetitiously denaturing, primer extending cycles as the second stage of PCR amplification, wherein an unrelated nucleic acids sequence to target sequence to be detected is added onto 5?-terminal of one PCR primer of each pair in extension.

Abstract: The present invention provides kits and microarrays containing primer pairs for amplifying drug resistance genes and/or probes for detection of drug resistance genes. Also provided are methods of detecting drug resistance genes using kits and microarrays described herein.

Abstract: The present invention discloses an asymmetric PCR amplification method, its special primer and application, aims to provide a simple, effective PCR amplification for preparation of single-stranded product. The asymmetric PCR primer of the invention comprises some PCR primer pairs, in which an unrelated nucleic acids sequence to target sequence to be detected is added onto 5?-terminal of one primer. The asymmetric PCR amplification provided includes the steps: 1) preparative denaturing; 2) repetitiously denaturing, primers annealing, extending cycles as the first stage of PCR amplification; 3) repetitiously denaturing, primer extending cycles as the second stage of PCR amplification, wherein an unrelated nucleic acids sequence to target sequence to be detected is added onto 5?-terminal of one PCR primer of each pair in extension.

Abstract: The present invention provides kits and microarrays containing primer pairs for amplifying drug resistance genes and/or probes for detection of drug resistance genes. Also provided are methods of detecting drug resistance genes using kits and microarrays described herein.