-
11.
公开(公告)号:US20190136293A1
公开(公告)日:2019-05-09
申请号:US16247323
申请日:2019-01-14
Applicant: GEN-PROBE INCORPORATED
Inventor: Michael R. Reshatoff , Edgar O. Ong , James J. Hogan
CPC classification number: C12Q1/68 , C12Q1/689 , C12Q2304/00 , Y02A50/451
Abstract: Provided are compositions, kits, and methods for the identification of Salmonella. In certain aspects and embodiments, the compositions, kits, and methods may provide improvements in relation to specificity, sensitivity, and speed of detection.
-
公开(公告)号:US09845509B2
公开(公告)日:2017-12-19
申请号:US14075944
申请日:2013-11-08
Applicant: Gen-Probe Incorporated
Inventor: Jennifer J. Bungo , James J. Hogan , Reinhold B. Pollner , Marie K. Hudspeth , Shannon K. Kaplan , Elizabeth M. Marlowe
IPC: C12Q1/68
CPC classification number: C12Q1/689 , C12Q1/686 , Y02A50/451
Abstract: Compositions are disclosed as nucleic acid sequences that may be used as amplification oligomers, including primers, and detection probes that hybridize specifically to Legionella pneumophila 23S rRNA sequences or DNA encoding 23S rRNA. Reaction mixtures are disclosed that contain oligonucleotides for the in vitro amplification and/or detection of Legionella pneumophila 23S rRNA sequences or DNA encoding 23S rRNA. Methods are disclosed for amplifying and/or detecting the presence of L. pnuemophila in samples by using the disclosed compositions in in vitro methods that include nucleic acid amplification and/or detection of a 23S rRNA sequence or DNA encoding the 23S rRNA sequence to produce a detectable amplification product. Reaction mixtures are disclosed that contain oligonucleotides for the in vitro amplification and/or detection of Legionella pneumophila 23S rRNA sequences or DNA encoding 23S rRNA.
-
公开(公告)号:US09765403B2
公开(公告)日:2017-09-19
申请号:US14938630
申请日:2015-11-11
Applicant: Gen-Probe Incorporated
Inventor: Shannon K. Kaplan , Kristin W. Livezey , Michael M. Becker , James J. Hogan
IPC: C12Q1/68
Abstract: Compositions, reaction mixtures, kits and methods used in amplifying and detecting nucleic acids from various species of the class Mollicutes. Particular regions of the 23S rRNA or its gene have been identified as preferred targets for nucleic acid amplification reactions of a sample suspected containing at least one species of Mollicutes. Some oligomers comprise tag regions, target closing regions, promoter sequences, and/or binding moieties. Samples can be from any source suspected of containing a species of the class Mollicutes. Preferred sample sources include bioreactors, cell lines, cell culture wares and pharmaceutical manufacturing wares.
-
-