669 research outputs found

    A system for calculating the greatest common denominator implemented using asynchrobatic logic

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    An asynchrobatic system that uses Euclid's algorithm to calculate the greatest common denominator of two numbers is presented. This algorithm is a simple system that contains both repetition and decision, and therefore demonstrates that asynchrobatic logic can be used to implement arbitrarily complex computational systems. Under typical conditions on a 0.35 mum process, a 16-bit implementation can perform a 24-cycle test vector in 2.067 mus with a power consumption of 3.257 nW

    Using positive feedback adiabatic logic to implement reversible Toffoli gates

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    A reversible, positive feedback adiabatic logic circuit is presented, which by implementing the universal Toffoli gate demonstrates that reversible logic circuits can be created and implemented using this adiabatic logic family. When compared to circuits with similar circuit structures that do not incorporate complete recovery logic, the use of reversible structures shows a reduction in energy losses by a mean of just under 63%

    An asynchrobatic, radix-four, carry look-ahead adder

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    A low-power, Asynchrobatic (asynchronous, quasi-adiabatic), sixteen-bit, radix-four, parallel-prefix adder circuit is presented. The results show that it is an efficient, low power design, and that as would be expected with an asynchronous design, its performance is determined by its operating conditions. On a 0.35 mum CMOS process, under ldquotypicalrdquo process conditions, operating at an effective frequency of 22 MHz, an addition can be performed using 69 pW, with 48.3 pW used by the control logic and 20.7 pW by the data-path

    A rapid method of cloning functional variable-region antibody genes in Escherichia coli as single-chain immunotoxins

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    We have devised a strategy based on polymerase chain reaction (PCR) for the rapid cloning of functional antibody genes as single-chain immunotoxins. RNA from a hybridoma producing an antibody (OVB3) that reacts with ovarian cancer cells was used as a template to make the first strand of a cDNA. Then a second strand was synthesized and amplified by using two sets of DNA primers that (i) hybridized to the ends of the light- and heavy-chain variable regions, (ii) encoded a linker peptide, and (iii) contained appropriate restriction enzyme sites for cloning. After 30 cycles of PCR, the DNA fragments containing sequences encoding the light- and heavy-chain variable regions were cloned into an Escherichia coli expression vector containing a portion of the Pseudomonas exotoxin gene. Clones encoding recombinant single-chain immunotoxins were expressed in E. coli and the protein product was assessed for its ability to bind to or kill cells bearing the OVB3 antigen. By using this approach it should be possible to rapidly clone the functional variable region sequences of many different antibodies from hybridoma RNA

    Sensitivity of selected organ dissection to diagnose Taenia solium cysticercosis in pigs from endemic areas

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    Taenia solium, also known as the pork tapeworm, is a neglected zoonotic parasite which is endemic in many developing countries, including Zambia. The tapeworm causes two disease conditions in humans: (1) taeniosis, which is the intestinal tapeworm infection, obtained after consumtion of raw/undercooked infected pork; and (2) cysticercosis, which is the metacestode larval stage infection, obtained after ingestion of tapeworm eggs. A human tapeworm carrier can excrete high numbers of eggs with the stool (100 000 eggs per day) and is thus an important source of environmental contamination. The transmission of cysticercosis is thus enhanced with poor sanitation and the lack of clean drinking water. After ingestion of the eggs, oncospheres hatch in the intestine and disseminate to several body tissues, including the central nervous system. Infection of the central nervous system with cysticerci is called neurocysticercosis, which is a major cause of acquired epilepsy worldwide

    Identification of two lysosomal membrane glycoproteins.

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