Abstract: An interface for use of device whose core circuitry operates in one voltage domain, but exchanges signal with another device (or “host”) according a different voltage domain, and the use of such an interface for supplying data using a double data rate (DDR) transfer, is presented. One concrete example of this situation is a memory card, where the internal circuitry uses one voltage range for its core operating voltages, but exchanges signals with a host using different, input/output voltage range. According to a general set of aspects, the interface receives data signals from the device at the device's core operating voltage domain, individually level shifts these to the input/output voltage domain, and then combines them into a DDR signal for transfer to the host device, where a (non-level shifted) clock signal from the host device is used as the select signal to form the DDR data signal.

Abstract: Disclosed are methods for identifying compounds that modulate an immune complex that includes a T cell receptor (TCR) and a major histocompatibility complex (MHC) antigen. The invention has many useful applications including providing high throughput screening assays for detecting compositions that can modulate an immune response.

Abstract: The present invention provides novel methods for the synthesis and isolation and purification of a peptide of interest (target peptide). In particular, the invention relates to peptide synthesis, isolation and purification methods that comprise use of penI fusion polypeptides and related gene fusion constructs that encode such polypeptides.

Abstract: The present invention provides novel methods for the synthesis and isolation and purification of a peptide of interest (target peptide). In particular, the invention relates to peptide synthesis, isolation and purification methods that comprise use of penI fusion polypeptides and related gene fusion constructs that encode such polypeptides.

Abstract: The present invention provides the nucleotide sequences of Acetobacter operons, cdg operons encoding genes for the biosynthesis and degradation of cyclic diguanosine monophosphate (c-di-GMP). Specifically, the nucleotide sequences and deduced amino acid sequences of 3 phosphodiesterases isozymes, 3 diguanylate cyclase isozymes, and 2 polypeptides of unidentified function are provided. Also provided for are various strains of microorganisms, including Acetobacter cells genetically manipulated so as to produce elevated and/or reduced levels of one or more cdg operon encoded proteins.

Abstract: An industrial automation system using transformers for providing electrical isolation between a system interface chip and a load interface chip while simultaneously allowing communication of power and data across the isolation barrier. Clock pulses are transmitted from the system interface chip to the load interface chip across one transformer, and the clock pulses are used by the load interface chip to create a power supply for operating the components within the chip. Data is communicated from the system interface chip to the load interface chip across a second transformer by the use of messages. Each message comprises a bit sync field, a byte sync field, and a data field. The bit sync field and byte sync field are used by the load interface chip to synchronize itself with the system interface chip.

Abstract: Novel proteins capable of binding to bacterial cellulose synthase are provided. Proteins that co-purify with bacterial cellulose synthase and have approximate relative molecular weights of 20 kDa, 54 kDa and 59 kDa are taught. Also provided for are nucleotide sequences encoding the proteins, antibodies to the proteins, and recombinant host cells for the expression of the cellulose synthase associated (co-purifying) proteins. The cellulose synthase associated proteins (CSAPs) CSAP20 (SEQ ID NO: 1) CSAP54 (SEQ ID NO: 2), and CSAP59 (SEQ ID NO: 3) are specifically provided for.

Abstract: Nucleic acid sequences encoding the bacterial cellulose synthase operon derived from Acetobacter are disclosed. Methods for isolating the genes, vectors containing the genes, and transformed hosts useful for the expression of recombinant bacterial cellulose synthase or production of cellulose are also described.