Abstract: A process is provided for printing a high resolution pattern on a photopolymeric surface.

Abstract: An activation method includes a security module card verifying an activation server using a shared secret key and a first challenge, mediating a verification of the activation server by a mobile device, and encrypting the second challenge using a generated key to obtain an encrypted second challenge. The security module card further transmits the encrypted second challenge and a third challenge to the mobile device. The method further includes receiving an encrypted third challenge from the mobile device, decrypting the encrypted third challenge to obtain a received third challenge, verifying the mobile device based on the received third challenge being equal to the third challenge sent to the mobile device, and sending a validation of mutual trust between the security module card and the mobile device to the activation server.

Abstract: An activation method includes a security module card verifying an activation server using a shared secret key and a first challenge, mediating a verification of the activation server by a mobile device, and encrypting the second challenge using a generated key to obtain an encrypted second challenge. The security module card further transmits the encrypted second challenge and a third challenge to the mobile device. The method further includes receiving an encrypted third challenge from the mobile device, decrypting the encrypted third challenge to obtain a received third challenge, verifying the mobile device based on the received third challenge being equal to the third challenge sent to the mobile device, and sending a validation of mutual trust between the security module card and the mobile device to the activation server.

Abstract: A process is provided for printing a high resolution pattern on a photopolymeric surface.

Abstract: The invention provides polypeptides, including enzymes, structural proteins and binding proteins, polynucleotides encoding these polypeptides, and methods of making and using these polynucleotides and polypeptides. Polypeptides, including enzymes and antibodies, and nucleic acids of the invention can be used in industrial, experimental, food and feed processing, nutritional and pharmaceutical applications, e.g., for food and feed supplements, colorants, neutraceuticals, cosmetic and pharmaceutical needs. Polypeptides of the invention can be used in food processing, brewing, bath additives, alcohol production, peptide synthesis, enantioselectivity, hide preparation in the leather industry, waste management and animal degradation, silver recovery in the photographic industry, medical treatment, silk degumming, biofilm degradation, biomass conversion to a biofuel (e.g., a bioethanol, biomethanol, biopropanol or biobutanol, a biodiesel, etc.

Abstract: The present fluid pumping method for micro-fluidic devices uses gas bubbles to move fluid by light beams. The light beams are emitted to the fluid near the gas bubble through an optically transparent cover and correspondingly heat the fluid in the micro channels. The liquid temperature variation changes the surface tension of the gas bubble near the heated fluid side, therefore, a pressure gradient between the end portions of the gas bubble generates accordingly. By moving the light beams, the moved pressure difference will be achieved, which will drive the gas bubbles and pump the fluid. Such a fluid pumping can simplify the structure of a micro-fluidic device and eliminate heat loss because of using a controllable light beam.

Abstract: A method of identification of differentially expressed messenger RNA (mRNA) which consists of synthesizing from a set of sequences of mRNA sets of fragments of complementary DNA (cDNA), which are separated with the aid of gel electrophoresis and the pictures of separation of the cDNA from different types of cells are compared and fragments with differential signal intensity are identified. For formation of the set of fragments the cDNA is cleaved with the aid of restriction nucleases. A method of cloning of differentially expressed mRNAs consists of synthesizing from sets of sequences of mRNAs from different types of cells sets of fragments of complementary DNA (cDNA) which are separated with the aid of gel electrophoresis, the pictures of the separation of the cDNA from different types of cells are compared, fragments of cDNA with different signal intensities are separated from the gel, amplified with the aid of a polymerase chain reaction and cloned to a plasmid or phage vector.