Abstract: Isotropic sensor 1, which comprises three sensor units 2, provided with a lead wire winding 3 surrounded by a conducting screen 4, the screen 4 being interrupted in two first zones I1, I2 diametrically opposite, there being in one of said zones I1, I2 the terminals VB for measuring the currents induced, wherein the two ends of each screen segment 41, 42 in the first two zones I1, I2 are connected two by two by means of conductors 5, 6 and comprises two second zones I3, I4 of interruption disposed at a halfway point of each screen segment 41, 42, in such a way that it is possible to measure at high frequencies simultaneously, independently and with precision, both magnetic field B and electric field E.

Abstract: Isotropic sensor 1, which comprises three sensor units 2, provided with a lead wire winding 3 surrounded by a conducting screen 4, the screen 4 being interrupted in two first zones I1, I2 diametrically opposite, there being in one of said zones I1, I2 the terminals VB for measuring the currents induced, wherein the two ends of each screen segment 41, 42 in the first two zones I1, I2 are connected two by two by means of conductors 5, 6 and comprises two second zones I3, I4 of interruption disposed at a halfway point of each screen segment 41, 42, in such a way that it is possible to measure at high frequencies simultaneously, independently and with precision, both magnetic field B and electric field E.

Abstract: Method for unamplified, selective identification of a microorganism comprising obtaining a sample comprising the microorganism, wherein the sample comprises unseparated genetic material of the microorganism; adding to the sample a molecular beacon comprising an nucleic sequence which is complementary to at least one nucleic acid sequence in the microorganism; and heating the sample; wherein the molecular beacon hybridizes with said nucleic acid sequence to produce a detectable signal.

Abstract: A method and apparatus for rapid and accurate detection and discrimination of biological, radiological, and chemical particles in air. A suspect aerosol of the target particulates is treated with a taggant aerosol of ultrafine particulates. Coagulation of the taggant and target particles causes a change in fluorescent properties of the cloud, providing an indication of the presence of the target.

Abstract: A method and apparatus for rapid and accurate detection and discrimination of biological, radiological, and chemical particles in air. A suspect aerosol of the target particulates is treated with a taggant aerosol of ultrafine particulates. Coagulation of the taggant and target particles causes a change in fluorescent properties of the cloud, providing an indication of the presence of the target.

Abstract: A method and device for collecting airborne particulate samples comprising vacuum air intake tube(s) onto the distal end of each of which is connected a regulating nozzle that is covered by the well reservoir of a capture vessel. Ambient air is directed to impact the interior surfaces of a single or multi-reservoir capture vessel. Each such well reservoir may include additional collector media and can be fitted with a filter screen. A plurality of said intake tubes may also be assembled and automated for programmable sample times and duration through a manifold in order to service a standard well tray which provides for higher collection efficiencies. In situ pathogen detection is possible by inclusion of nucleic acid specific dyes or probes in the media and/or by attachment of an excitation light, radiation detector, or fluorometer device(s) focused on the internal surfaces of a semi-translucent well reservoir.

Abstract: A method for rapid and efficient detection of a target DNA or RNA sequence is provided. A primer having a 3′-hydroxyl group at one end and having a sequence of nucleotides sufficiently homologous with an identifying sequence of nucleotides in the target DNA is selected. The primer is hybridized to the identifying sequence of nucleotides on the DNA or RNA sequence and a reporter molecule is synthesized on the target sequence by progressively binding complementary nucleotides to the primer, where the complementary nucleotides include nucleotides labeled with a fluorophore. Fluorescence emitted by fluorophores on single reporter molecules is detected to identify the target DNA or RNA sequence.