Patent classifications
C12Q1/6818
MARINE DNA POLYMERASE I
The present invention relates to DNA polymerases. In particular, the present invention relates to heat labile DNA polymerases of marine origin, having high polymerase activity, strand displacement activity and 3-5′ exonuclease activity. Furthermore, the present invention provides heat labile DNA polymerases substantially without strand-displacement activity.
MULTIPLEX DETECTION OF NUCLEIC ACIDS USING MIXED REPORTERS
The present invention provides oligonucleotides and methods for their use in the detection and/or differentiation of target nucleic acids. The oligonucleotides and methods find particular application in amplifying, detecting, and/or discriminating multiple targets simultaneously.
MULTIPLEX DETECTION OF NUCLEIC ACIDS USING MIXED REPORTERS
The present invention provides oligonucleotides and methods for their use in the detection and/or differentiation of target nucleic acids. The oligonucleotides and methods find particular application in amplifying, detecting, and/or discriminating multiple targets simultaneously.
MULTIPLEX DETECTION OF NUCLEIC ACIDS USING MIXED REPORTERS
The present invention provides oligonucleotides and methods for their use in the detection and/or differentiation of target nucleic acids. The oligonucleotides and methods find particular application in amplifying, detecting, and/or discriminating multiple targets simultaneously.
SENSOR FOR SIMULTANEOUS CHEMICAL, BIOLOGICAL, AND RADIOLOGICAL/NUCLEAR DETECTION
A multifunctional biosensor is described that is configured to simultaneously detect two or more different types of chemical, biological and/or radiological/nuclear (CBRN) threats on one platform using FRET-based and/or NSET-based technology.
SENSOR FOR SIMULTANEOUS CHEMICAL, BIOLOGICAL, AND RADIOLOGICAL/NUCLEAR DETECTION
A multifunctional biosensor is described that is configured to simultaneously detect two or more different types of chemical, biological and/or radiological/nuclear (CBRN) threats on one platform using FRET-based and/or NSET-based technology.
Oligonucleotide-functionalized hydrophobic polymer nanoparticles
The present invention concerns an oligonucleotide-functionalized hydrophobic polymer nanoparticle and method of its preparation. Said nanoparticle is a dye-loaded polymeric nanoparticle, and being functionalized by: (a) target-specific oligonucleotides, and/or (b) non-specific oligonucleotides.
Oligonucleotide-functionalized hydrophobic polymer nanoparticles
The present invention concerns an oligonucleotide-functionalized hydrophobic polymer nanoparticle and method of its preparation. Said nanoparticle is a dye-loaded polymeric nanoparticle, and being functionalized by: (a) target-specific oligonucleotides, and/or (b) non-specific oligonucleotides.
Oligonucleotide-functionalized hydrophobic polymer nanoparticles
The present invention concerns an oligonucleotide-functionalized hydrophobic polymer nanoparticle and method of its preparation. Said nanoparticle is a dye-loaded polymeric nanoparticle, and being functionalized by: (a) target-specific oligonucleotides, and/or (b) non-specific oligonucleotides.
Luminescence hybridisation assay method
This invention relates to a bioassay method for detecting and/or quantitating a short single-stranded nucleic acid analyte employing a binary probe system, where at least one of the two discrete oligonucleotide probe parts of the binary probe has partially double-stranded (self-complementary) stem-loop structure at one terminus and single-stranded overhang sequence region at the other terminus, where the single-stranded terminal regions of both discrete parts of the binary probe hybridize to adjacent complementary regions in the sequence of the nucleic acid analyte molecule, and at least one discrete part of the binary probe comprising a stem-loop structure and single-stranded overhang sequence region hybridizes to terminal region in the sequence of the nucleic acid analyte molecule forming a nick structure. The binary probe system employed in the bioassay method is based on a luminescent reporter technology, either lanthanide chelate complementation or resonance energy transfer with lanthanide label as a donor. Thereby the method allows detection and/or quantitation of the short nucleic acid analyte molecule by time-resolved fluorometry.