Abbott Molecular Inc.

Abbott Laboratories Corporation

Klara Abravaya

Ning Tang

Shihai X Huang

John A Salituro

Hong Wang

Joshua Kostera

Jacek J Gorzowski

Brian J Erickson

John R Hackett

Wai-Bing X Mak

Robert J Hoenle

Jennifer J Moore

Paul E Kroeger

Larry E Morrison

Gregor W Leckie

Vihanga Pahalawatta

Andrea Frank

Ka-Cheung X Luk

Claudia A Esping

Wesley Grimm

Robert Hillman

Sushil G Devare

Ekaterina Pestova

Priscilla Swanson

Kimberly Wilber-Mader

Barbara J Harris

Adam Koch

Madhuri Lucas

Claudia A Cygan Esping

John Hackett

Claudia Esping

Robert Hoenle

The disclosure is directed to kits and methods for amplifying and detecting human papilloma virus (HPV) of genotype 16, 18, 31, 33, 35, 39, 45, 51, 52, 56, 58, 59, 66, and/or 68 in a sample, which comprises a variety of combinations of forward oligonucleotide primers, reverse oligonucleotide primers, and oligonucleotide probes.

Assay for detecting human papilloma virus (HPV)

Provided herein are compositions and methods for diagnosing and characterizing tuberculosis infection. In particular, provided herein are compositions and methods for identifying drug resistant tuberculosis.

Compositions and methods for identifying drug resistant tuberculosis

The present invention relates to primers, probes, primer sets, primer and probe sets, methods and kits for detecting human papillomaviruses, human beta globin sequences and human papillomaviruses and human beta globin sequences in a test sample.

Primers and probes for detecting human papillomavirus and human beta globin sequences in test samples

A double-stranded nucleic acid hybridization probe and methods of using the same are described. The probe described is particularly suited for real-time RT-PCR reactions and has high tolerance to mismatches.

Double stranded linear nucleic acid probe

Disclosed herein are hybridization buffer compositions and hybridization compositions, methods of making the compositions, and methods of using the compositions, such as the hybridization of DNA or RNA sequences by fluorescence in situ hybridization ('FISH').

Hybridization buffers

Oligonucleotide primer sets, probes, and combinations of the primer sets and probes are provided herein. These reagents are useful for amplifying and detecting HIV-1 target sequences in a test sample.

Amplification and detection reagents for HIV-1

Probe sequences that are useful for detecting oncogenic HPV types 16, 18, 31, 33, 35, 39, 45, 51, 52, 56, 58, 59 and 68 are herein provided. These sequences can be used in hybridization assays or amplification based assays designed to detect the presence of these oncogenic HPV types in a test sample. Additionally, the sequences can be provided as part of a kit.

Nucleic acid primers and probes for detecting oncogenic human papillomaviruses

Provided herein are primer/probe sets useful for detecting HIV (i.e. either or both HIV 1 or HIV 2) in a test sample. The primer/probe sets are can be employed according to nucleic acid amplification procedures including PCR or RT PCR. The primer/probe sets can also be provided in the form of a kit with other reagents for performing a nucleic acid amplification reaction.

Nucleic acid primers and probes for detecting HIV-1 and HIV-2

Growing community of inventors

Kenilworth, IL, United States of America

Klara Abravaya