Abstract: The present application provides a high-wear-resistance far-infrared ceramic polished glazed tile and preparation method therefor. The preparation method includes application of far-infrared overglaze, ink-jet printing, application of transparent far-infrared polished glaze and application of abrasion-resistant far-infrared polished glaze in sequence on a body, firing, and polishing. By adopting the far-infrared overglaze, the transparent far-infrared polished glaze and the abrasion-resistant far-infrared polished glaze in combination, the polished glaze tile can have a far-infrared function, high transparency, and high abrasion resistance.

Abstract: The present invention relates to a rapid detection of microbial-associated nuclease activity with chemically modified nuclease (e.g., endonuclease) substrates, and probes and compositions useful in detection assays.

Abstract: The present invention relates to a rapid detection of microbial-associated nuclease activity with chemically modified nuclease (e.g., endonuclease) substrates, and probes and compositions useful in detection assays.

Abstract: Disclosed are a semi-transparent ceramic sheet decorated through ink light-absorbance and a preparation method thereof. The semi-transparent ceramic sheet comprises a semi-transparent green body, an inner inkjet pattern layer infiltrating into the semi-transparent green body from an upper surface of the semi-transparent green body, a decoloration glaze layer located on the upper surface, and a surface pattern layer located on the decoloration glaze layer. The decoloration glaze layer is capable of decoloring the ink of the inner inkjet pattern layer. The semi-transparent ceramic sheet is provided with the decoloration glaze layer so that the inkjet decoration of the inner inkjet pattern layer cannot be displayed on the surface, and the decorative pattern on the surface of the green body is the surface pattern layer and the inner inkjet pattern layer is completely in the inner layer of the green body.

Abstract: In an embodiment, a method of payload matching via a single pass transformation of an HTTP payload includes receiving a payload packet destined for a recipient and parsing the payload packet in a single scan of the packet using a combined regular expression. The combined regular expression includes a plurality of regular expressions that correspond to a set of replacement rules. The method includes determining a scatter-gather list conforming to the rule, constructing a new payload packet based on the scatter-gather list, and sending the new payload packet to the recipient.

Abstract: The present invention relates to a rapid detection of microbial-associated nuclease activity with chemically modified nuclease (e.g., endonuclease) substrates, and probes and compositions useful in detection assays.

Abstract: The present invention relates to a rapid detection of microbial-associated nuclease activity with chemically modified nuclease (e.g., ribonuclease) substrates, and probes and compositions useful in detection assays.

Abstract: Disclosed are a semi-transparent ceramic sheet decorated through ink light-absorbance and a preparation method thereof. The semi-transparent ceramic sheet comprises a semi-transparent green body, an inner inkjet pattern layer infiltrating into the semi-transparent green body from an upper surface of the semi-transparent green body, a decoloration glaze layer located on the upper surface, and a surface pattern layer located on the decoloration glaze layer. The decoloration glaze layer is capable of decoloring the ink of the inner inkjet pattern layer. The semi-transparent ceramic sheet is provided with the decoloration glaze layer so that the inkjet decoration of the inner inkjet pattern layer cannot be displayed on the surface, and the decorative pattern on the surface of the green body is the surface pattern layer and the inner inkjet pattern layer is completely in the inner layer of the green body.

Abstract: The present invention relates to a rapid detection of microbial-associated nuclease activity with chemically modified nuclease (e.g., endonuclease) substrates, and probes and compositions useful in detection assays.

Abstract: In an embodiment, a method of payload matching via a single pass transformation of an HTTP payload includes receiving a payload packet destined for a recipient and parsing the payload packet in a single scan of the packet using a combined regular expression. The combined regular expression includes a plurality of regular expressions that correspond to a set of replacement rules.

Abstract: The present invention relates to a rapid detection of microbial-associated nuclease activity with chemically modified nuclease (e.g., ribonuclease) substrates, and probes and compositions useful in detection assays.

Abstract: The present invention relates to a rapid detection of microbial-associated nuclease activity with chemically modified nuclease (e.g., ribonuclease) substrates, and probes and compositions useful in detection assays. Accordingly, in certain embodiments, the present invention provides a probe for detecting a microbial endonuclease comprising a substrate oligonucleotide of 2-30 nucleotides in length, a fluorescence-reporter group operably linked to the oligonucleotide, and a fluorescence-quencher group operably linked to the oligonucleotide. The fluorescence-reporter group and the fluorescence-quencher group are separated by at least one RNAse-cleavable residue, e.g., RNA base.

Abstract: The present invention relates to a rapid detection of microbial-associated nuclease activity with chemically modified nuclease (e.g., endonuclease) substrates, and probes and compositions useful in detection assays.

Abstract: The present invention relates to a rapid detection of microbial-associated nuclease activity with chemically modified nuclease (e.g., ribonuclease) substrates, and probes and compositions useful in detection assays. Accordingly, in certain embodiments, the present invention provides a probe for detecting a microbial endonuclease comprising a substrate oligonucleotide of 2-30 nucleotides in length, a fluorescence-reporter group operably linked to the oligonucleotide, and a fluorescence-quencher group operably linked to the oligonucleotide. The fluorescence-reporter group and the fluorescence-quencher group are separated by at least one RNAse-cleavable residue, e.g., RNA base.

Abstract: A system and method for facilitating anti-replay protection with multi-sender traffic is disclosed. The system employs time-based anti-replay protection wherein a sender transmits a data packet with a pseudo-timestamp encapsulated in a metadata payload. At the receiving end, the receiver compares the pseudo-timestamp information received with its own pseudo-time, determines if a packet is valid, and rejects a replay packet. The pseudo-time information is transmitted through the metadata payload and new fields need not be added to the IPSec (IP Security) Protocol, thus the existing hardware can be employed without any changes or modifications.

Abstract: The invention provides novel anthraquinone compositions that are useful as broad-spectrum quenchers of fluorescence and provides methods for making and using them. The anthraquinone quenchers can be conjugated to a variety of biologically relevant compounds, including lipids, nucleic acids, polypeptides, and more specifically antigens, steroids, vitamins, drugs, haptens, metabolites, toxins, environmental pollutants, amino acids, peptides, proteins, nucleotides, oligonucleotides, polynucleotides, carbohydrates, and their analogs. The invention also provides kits comprising, in one or more containers, at least one anthraquinone quencher dye composition of the present invention, and instructions for using that composition.

Abstract: This invention pertains to methods for cloning microRNA (miRNA) and other small ribonucleic acid (RNA) species from relevant cell sources.

Abstract: The invention provides novel anthraquinone compositions that are useful as broad-spectrum quenchers of fluorescence and provides methods for making and using them. The anthraquinone quenchers can be conjugated to a variety of biologically relevant compounds, including lipids, nucleic acids, polypeptides, and more specifically antigens, steroids, vitamins, drugs, haptens, metabolites, toxins, environmental pollutants, amino acids, peptides, proteins, nucleotides, oligonucleotides, polynucleotides, carbohydrates, and their analogs. The invention also provides kits comprising, in one or more containers, at least one anthraquinone quencher dye composition of the present invention, and instructions for using that composition.

Abstract: This invention pertains to methods for cloning microRNA (miRNA) and other small ribonucleic acid (RNA) species from relevant cell sources.

Abstract: The invention provides novel anthraquinone compositions that are useful as broad-spectrum quenchers of fluorescence and provides methods for making and using them. The anthraquinone quenchers can be conjugated to a variety of biologically relevant compounds, including lipids, nucleic acids, polypeptides, and more specifically antigens, steroids, vitamins, drugs, haptens, metabolites, toxins, environmental pollutants, amino acids, peptides, proteins, nucleotides, oligonucleotides, polynucleotides, carbohydrates, and their analogs. The invention also provides kits comprising, in one or more containers, at least one anthraquinone quencher dye composition of the present invention, and instructions for using that composition.