Patent classifications
B01D57/02
PROCESS TECHNOLOGY FOR BIOLOGICAL PRODUCT MANUFACTURING AND DOWNSTREAM PURIFICATION
Provided herein are, inter alia, biological manufacturing and downstream purification processes.
PROCESS TECHNOLOGY FOR BIOLOGICAL PRODUCT MANUFACTURING AND DOWNSTREAM PURIFICATION
Provided herein are, inter alia, biological manufacturing and downstream purification processes.
Carbon, nitrogen and oxygen separator and method of use thereof
An apparatus and a method for producing carbon, oxygen and optionally nitrogen from treated flue gases are provided. The apparatus provides a thermo-dielectric-electric field that splits molecules of carbon dioxide and carbon monoxide into carbon and oxygen and nitrogen oxides into nitrogen and oxygen. The carbon is recovered in a variety of solid forms, and oxygen and nitrogen are recovered as gases.
Carbon, nitrogen and oxygen separator and method of use thereof
An apparatus and a method for producing carbon, oxygen and optionally nitrogen from treated flue gases are provided. The apparatus provides a thermo-dielectric-electric field that splits molecules of carbon dioxide and carbon monoxide into carbon and oxygen and nitrogen oxides into nitrogen and oxygen. The carbon is recovered in a variety of solid forms, and oxygen and nitrogen are recovered as gases.
Device and method for isotachophoretic focusing large sample volumes
The present invention provides, in some embodiments, an isotachophoresis (ITP) apparatus, a kit comprising same and method of use thereof for the focusing analytes of interest from large sample volumes.
Device and method for isotachophoretic focusing large sample volumes
The present invention provides, in some embodiments, an isotachophoresis (ITP) apparatus, a kit comprising same and method of use thereof for the focusing analytes of interest from large sample volumes.
Large-scale controllable preparation method for plasmonic nanonail structure
A controllable preparation method for a plasmonic nanonail structure is provided. A size of a nanomaterial can be controlled at sub-wavelength. The nanomaterial has good localized surface plasmon resonance effect, and the optical, electrical and mechanical properties of the nanometer material all can be regulated. The plasmonic nanonail is composed of two parts, i.e., a silver nanorod, a gold nanorod or a silver-gold-silver alloy nanorod and an approximate equilateral triangular nano-silver plate growing on the nanorod. A length of the nanorod is controlled within 20-30 nanometers, a diameter of the nanorod is controlled within 10-200 nanometers, a side length of the triangular nano-silver plate is controlled within 20 nanometers to 2 microns, and a size of the triangular plate is less than or equal to the length of the nanorod.
Large-scale controllable preparation method for plasmonic nanonail structure
A controllable preparation method for a plasmonic nanonail structure is provided. A size of a nanomaterial can be controlled at sub-wavelength. The nanomaterial has good localized surface plasmon resonance effect, and the optical, electrical and mechanical properties of the nanometer material all can be regulated. The plasmonic nanonail is composed of two parts, i.e., a silver nanorod, a gold nanorod or a silver-gold-silver alloy nanorod and an approximate equilateral triangular nano-silver plate growing on the nanorod. A length of the nanorod is controlled within 20-30 nanometers, a diameter of the nanorod is controlled within 10-200 nanometers, a side length of the triangular nano-silver plate is controlled within 20 nanometers to 2 microns, and a size of the triangular plate is less than or equal to the length of the nanorod.
METHOD AND DEVICE FOR DETERMINING THE CONCENTRATION OF ANALYTES IN WHOLE BLOOD
A method and system for determining a concentration of one or more analytes in whole blood is provided. In one aspect of the invention, the system includes a channel configured to carry whole blood. The system further includes a light source configured to emit light on the channel. Additionally, the system includes an actuation module associable with the channel, wherein the actuation module is configured to generate a cell-free plasma layer in the channel. Furthermore, the system includes an optical module associable with the channel.
Methods for electroelution of biomolecules
A method of eluting biomolecules, such as nucleic acids from a biological sample by electroelution is provided. An example of a method includes various steps, such as loading the biological sample to a device comprising a housing, at least two conductive redox polymer electrodes operationally coupled to the housing and a biomolecule impermeable layer disposed on at least one of the electrodes. The loading of sample is followed by initiating an electrical connection to generate an electric field strength sufficient to elute biomolecules from the biological sample; and eluting the biomolecules from the biological sample.