Abstract: Chiral peptide nucleic acids are provided which hybridise strongly with complementary nucleic acids and have potential as antigene and antisense agents and as tools in molecular biology. The compounds have the formulae.
where
n is 1 to 200,
B is a protected or unprotected base,
X may be OH,
Y may be H, and R′ and R″, which are the same or different, are H, C1-C6 alkyl, aryl or aralkyl or R′ or R″, together the carbon atoms to which they are attached, form a cycloalkyl ring and protected derivatives thereof.
Abstract: A portable polymerase chain reaction DNA amplification and detection system includes one or more chamber modules. Each module supports a duplex assay of a biological sample. Each module has two parallel interrogation ports with a linear optical system. The system is capable of being handheld.
Type:
Grant
Filed:
December 29, 2000
Date of Patent:
March 2, 2004
Assignee:
The Regents of the University of California
Inventors:
William J. Benett, James B. Richards, Paul L. Stratton, Dean R. Hadley, Fred P. Milanovich, Phil Belgrader, Peter L. Meyer
Abstract: The present invention discloses a one-pot, high-throughput method for the measurement of the amount of a nucleotide generated in a cell. The method is particularly effective in measuring changes in cyclic adenosine 3′,5′-monophosphate (cAMP) coupled to cell receptors in insects.
Abstract: The present invention relates to three sets of novel primers of SEQ ID Nos. 1-6, wherein said three sets of primer are designed from three genes omt, ord, and afl R respectively of aflatoxin biosynthesis pathway of fungi Aspergillus flavus and an improved method of identifying aflatoxinogenic aspergilli using said three sets of primers.
Type:
Grant
Filed:
March 27, 2002
Date of Patent:
September 23, 2003
Assignee:
Council of Scientific and Industrial Research
Abstract: The present invention relates to methods and compositions for analyzing nucleic acids. In particular, the invention provides for methods and combinations for analyzing nucleic acids in a plurality of samples using a plurality of detectably different signature labels and a probe that is hybridizable to each of the target nucleic acids. The invention also provides for a method for quantifying a nucleic acid by analyzing the amount of a label, e.g., a photoactivatable label, attached to the target nucleic acid.
Abstract: The invention provides methods to detect Group A Streptococcus (GAS) in biological samples using real-time PCR. Primers and probes for the detection of GAS are provided by the invention. Articles of manufacture containing such primers and probes for detecting GAS are further provided by the invention.
Type:
Grant
Filed:
February 20, 2002
Date of Patent:
July 15, 2003
Assignee:
Mayo Foundation for Medical Education and Research