Abstract: An LED Christmas lamp includes a lamp base, in which a receiving cavity is formed and having coupling slots formed in a cavity wall to receive and retain metal plates on ends of four conductive wires. A light source holder has a top forming a light disposition section, in which three receiving holes are formed and has a bottom on which a fitting section having four bearing surfaces is formed. The fitting section has a bottom face including six through apertures. Three LED illuminants are provided, each having two terminal pins, and are respectively inserted into the three receiving holes with the terminal pins bent and positioned against the bearing surfaces of the fitting section so that when the light source holder is inserted into the receiving cavity, the terminal pins are set in electrical engagement with the metal plates of the conductive wires.

Abstract: Disclosed herein are tools and techniques for using a single-finger single touch to zoom content. In one embodiment disclosed herein, a single-finger single touch on a touch screen displaying at least a page of content is detected. At least in response to the detecting the single-finger single touch, a page zoom is performed.

Abstract: Presented herein are polymerase enzymes for improved incorporation of nucleotide analogues, in particular nucleotides which are modified at the 3? sugar hydroxyl, as well as methods and kits using the same.

Abstract: A pointer tool in a touch-screen display is disclosed. The method includes activating a pointer tool in a touch screen display in response to contact with an area of the touch screen and persisting the displaying of the pointer tool in the touch screen display after the contact with the touch screen is removed. Once editing data is received, the pointer tool is removed from the touch screen display.

Abstract: The present disclosure relates to a clottable concentrate of platelet growth factors for therapeutic and/or cosmetic use, preferably comprising the growth factors PDGF, TGT-?, IGF, EGF, CTGF, bFGF and VEGF. In a preferred embodiment, the clottable concentrate of platelet growth factors does not induce blood cell-related transfusion reactions. The present disclosure also relates to a method for preparing a clottable concentrate of platelet growth factors including the steps of contacting a platelet concentrate with a solvent and/or a detergent, incubating the platelet concentrate with the solvent and/or detergent for a period of at least 5 minutes to 6 hours, at a pH maintained in a range from about 6.0 to about 9.0, and at a temperature within the range of from 2° C. to 50° C., preferably within the range of from 25° C. to 45° C., and removing the solvent and/or the detergent by oil extraction and/or chromatographic means.

Abstract: A method of distinguishing nucleotide sequences for different nucleic acid molecules including the steps of (a) mixing a plurality of different nucleic acid molecules with polymerase molecules and nucleotide molecules, wherein the different nucleic acid molecules are attached to a surface in the form of an array of nucleic acid features; (b) determining a transient state of the polymerase molecules at the nucleic acid features; and (c) identifying a subset of nucleic acid features that correctly incorporate the nucleotide molecules based on the transient state of the polymerase molecules at the nucleic acid features, thereby distinguishing the nucleotide sequences for the different nucleic acid molecules.

Abstract: Provided herein are compositions and systems for use in polymerase-dependent, nucleotide transient-binding methods. The methods are useful for deducing the sequence of a template nucleic acid molecule and single nucleotide polymorphism (SNP) analyses. The methods rely on the fact that the polymerase transient-binding time for a complementary nucleotide is longer compared to that of a non-complementary nucleotide. The labeled nucleotides transiently-binds the polymerase in a template-dependent manner, but does not incorporate. The methods are conducted under any reaction condition that permits transient binding of a complementary or non-complementary nucleotide to a polymerase, and inhibits nucleotide incorporation.

Abstract: Presented herein are polymerase enzymes for improved incorporation of nucleotide analogues, in particular nucleotides which are modified at the 3? sugar hydroxyl, as well as methods and kits using the same.

Abstract: A method of nucleic acid sequencing. The method can include the steps of (a) providing a polymerase tethered to a solid support charge sensor; (b) providing one or more nucleotides, whereby the presence of the nucleotide can be detected by the charge sensor; and (c) detecting incorporation of the nucleotide into a nascent strand complementary to a template nucleic acid.

Abstract: Presented herein are polymerase enzymes for improved incorporation of nucleotide analogues, in particular nucleotides which are modified at the 3? sugar hydroxyl, as well as methods and kits using the same.

Abstract: Provided herein is a method of amplifying nucleic acids using a plurality of modified nucleotides one or more of the nucleotides comprising a 3? blocking group. Also provided is a method of amplifying nucleic acids using oligonucleotide primers one or both of the primers comprising a 3? blocking group on one or more of the nucleotides of the primers.

Abstract: Disclosed herein are modified polymerase compositions exhibiting altered polymerase activity, which can be useful in a variety of biological applications. Also disclosed herein are methods of making and using such compositions. In some embodiments, the compositions exhibit altered properties that can enhance their utility in a variety of biological applications. Such altered properties, can include, for example, altered nucleotide binding affinities, altered nucleotide incorporation kinetics, altered photostability and/or altered nanoparticle tolerance, as well as a range of other properties as disclosed herein.

Abstract: An LED Christmas lamp includes a lamp base, in which a receiving cavity is formed and having coupling slots formed in a cavity wall to receive and retain metal plates on ends of four conductive wires. A light source holder has a top forming a light disposition section, in which three receiving holes are formed and has a bottom on which a fitting section having four earing surfaces is formed. The fitting section has a bottom face including six through apertures. Three LED illuminants are provided, each having two terminal pins, and are respectively inserted into the three receiving holes with the terminal pins bent and positioned against the bearing surfaces of the fitting section so that when the light source holder is inserted into the receiving cavity, the terminal pins are set in electrical engagement with the metal plates of the conductive wires.

Abstract: Various technologies for managing mobile device communications can be offered to implement a virtual personal operator. Incoming calls and texts can be managed intelligently based on a rich network-stored context, allowing the network to make decisions and interact with callers. Because context is stored by the network, the virtual personal operator can function without contacting the called mobile phone, and can even provide helpful information to callers if the mobile phone is offline. Rich do-not-disturb functionality can be provided, and privileged callers can be given additional information or functionality based on their privileged status. Numerous other features that assist with communications management can be supported.

Abstract: The invention concerns human platelet extracts rich in growth factors (PGF) for wound healing and stem cell expansion. Accordingly the subject invention relates to a virally-inactivated growth factors-containing platelet lysate depleted of PDGF and VEGF, which is preferably enriched in TGF, IGF and EGF-rich. The present invention further concerns a method for obtaining a platelet lysate comprising the steps of contacting a starting platelet concentrate with a solvent and/or a detergent, incubating the starting platelet concentrate with the solvent and/or detergent for a period of at least 5 minutes to 6 hours, at a pH maintained in a range from about 6.0 to about 9.0, and at a temperature within the range of from 2° C. to 50° C., optionally removing the solvent and/or the detergent by oil extraction and obtaining an aqueous protein phase, and incubating the solvent and/or detergent-treated platelet concentrate or the aqueous protein phase with charcoal.

Abstract: Provided herein are systems and methods for nucleotide incorporation reactions. The systems comprise polymerases having altered nucleotide incorporation kinetics and are linked to an energy transfer donor moiety, and nucleotide molecules linked with at least one energy transfer acceptor moiety. The donor and acceptor moieties undergo energy transfer when the polymerase and nucleotide are proximal to each other during nucleotide binding and/or nucleotide incorporation. As the donor and acceptor moieties undergo energy transfer, they generate an energy transfer signal which can be associated with nucleotide binding or incorporation. Detecting a time sequence of the generated signals, or the change in the signals, can be used to determine the order of the incorporated nucleotides, and can therefore be used to deduce the sequence of the target molecule.

Abstract: Provided herein are systems and methods for nucleotide incorporation reactions. The systems comprise polymerases having altered nucleotide incorporation kinetics and are linked to an energy transfer donor moiety, and nucleotide molecules linked with at least one energy transfer acceptor moiety. The donor and acceptor moieties undergo energy transfer when the polymerase and nucleotide are proximal to each other during nucleotide binding and/or nucleotide incorporation. As the donor and acceptor moieties undergo energy transfer, they generate an energy transfer signal which can be associated with nucleotide binding or incorporation. Detecting a time sequence of the generated signals, or the change in the signals, can be used to determine the order of the incorporated nucleotides, and can therefore be used to deduce the sequence of the target molecule.

Abstract: An automatic software audit system includes a client and a server. The client includes a network interface, a software installation record database, a software audit rule database, a software release database and a central processing unit (CPU). The network interface is coupled to the client. The software installation record databases stores a software installation record of the client. The software audit rule database stores a software audit rule. The software release database stores a software release record of the client. The CPU installs an agent program to the client to collect the software installation record, and generates a software audit result of the client according to the software installation record, the software audio rule and the software release record.

Abstract: A system and a method for stress detection on small areas are disclosed. The method is applied to a strain gauge, which uses the Joule heating effect-generated temperature difference to monitor and to localize compressive and tensile strains. Furthermore, the invention provides a systematic extrapolation prediction methodology for strains.

Abstract: An electronic system is provided. The electronic system includes a first electronic device and a second electronic device. The first electronic device includes a first display unit and a first processing unit. The first processing unit is used to run a first operating system. The second electronic device includes a second processing unit. The second processing unit is used to run a second operating system. The first electronic device and the second electronic device independently run the first operating system and the second operating system. When the first electronic device is electrically connected to the second electronic device, a state of the first operating system and the second operating system are respectively maintained and are selectively displayed on the first display unit.