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US 2026/0258509 A1Published application
Compositions and methods for detection of neisseria gonorroheae
AssigneeRoche Molecular Systems, Inc.
InventorsEllen H. Fiss Hobart, Jingtao Sun
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Abstract
Methods for the rapid detection of the presence or absence of NG Pilin Inverting protein (PivNg) gene in a biological or non-biological sample are described. The methods can include performing an amplifying step, a hybridizing step, and a detecting step. Furthermore, primers, probes targeting the NG PivNg genes, along with kits are provided that are designed for the detection of Neisseria gonorrhoeae (NG).
Claims17
A method of detecting Neisseria Gonorroheae (NG) in a sample, the method comprising:
- performing an amplifying step comprising contacting the sample with a set of NG PivNg gene primers to produce an amplification product if NG PivNg nucleic acid is present in the sample;
- performing a hybridizing step comprising contacting the amplification product with one or more detectable NG PivNg gene probes;
- and
- detecting the presence or absence of the amplification product, wherein the presence of the amplification product is indicative of the presence of NG in the sample and wherein the absence of the amplification product is indicative of the absence of NG in the sample;
- wherein the set of NG PivNg gene primers comprise a first primer comprising a first oligonucleotide sequence of SEQ ID NOs:
- 1, or a complement thereof, and a second primer comprising a second oligonucleotide sequence of SEQ ID NOs:
- 2, or a complement thereof;
- and
- wherein the one or more detectable NG PivNg gene probes comprises a third oligonucleotide sequence of SEQ ID NOs:
- 3, or the complement thereof.
7 more elements
A kit for detecting a nucleic acid of Neisseria Gonorroheae (NG) comprising:
- a first primer comprising a first oligonucleotide sequence of SEQ ID NOs:
- 1, or a complement thereof;
- a second primer comprising a second oligonucleotide sequence of SEQ ID NOs:
- 2, or a complement thereof;
- and
- a fluorescently detectably labeled probe comprising a third oligonucleotide sequence of SEQ ID NOs:
- 3, or a complement thereof, the detectably labeled probe configured to hybridize to an amplicon generated by the first primer and the second primer.
4 more elements
Dependencies are inferred from the claim text.