DEVICE:cobas® 4800 HPV Amplification/Detection Kit

Human papillomavirus (HPV) high risk strain nucleic acid IVD, kit, nucleic acid technique (NAT)

Aptima HPV Assay - Hologic

General Information Aptima™. 1. Aptima Transfer Solution (Tigris DTS System and Panther System only) Treated samples may be stored at 2°C to 8°C for up to 17 days prior to testing with the Aptima HPV assay. Refer to the Aptima Specimen Transfer kit package insert for further details.

Nucleic Acid Sequence-Based Amplification Assay for

Human papillomavirus (HPV) E6/E7 mRNA has been proposed as a more specific marker for cervical dysplasia and cancer than HPV DNA. This study evaluated the RNA specificity of nucleic acid sequence-based amplification (NASBA)-based HPV detection using HPV DNA plasmids (HPV type 16 [HPV16], HPV18, HPV31, HPV33, and HPV45) and nucleic acid extracts of several cell lines, which

AccuPower® HPV 16&18 Real-Time PCR Kit

AccuPower ® HPV 16&18 Real-Time PCR Kit includes Positive Control (PC), No Template Control (NTC) and Internal Positive Control (IPC) for accurate and reliable diagnosis of HPV 16 and 18. AccuPower ® HPV 16&18 Real-Time PCR Kit test results using clinical samples. The kit employs IPC in all wells to confirm correct PCR amplification.

QIAamp Circulating Nucleic Acid Kit - QIAGEN Online Shop

The QIAamp Circulating Nucleic Acid Kit efficiently purifies and concentrates free-circulating DNA, RNA, miRNA, and viral nucleic acids from starting materials that contain low concentrations of mostly fragmented DNA and RNA (typically 1–100 ng/ml circulating DNA in human plasma). Starting sample volumes can be up to 5 ml.

Molecular Diagnostics of Human Papillomavirus

Molecular Diagnostics of Human Papillomavirus Ashley Arney, MT(ASCP)CM. PCR and nucleic acid hybridization and Corbett Rotor-Gene 6600. Like all of the previous commercially available target amplification assays, the GenoID kit is not FDA approved. However, it has been CE-Marked for in vitro diagnostic use in Europe.

HPV Testing Solutions - Primary HPV Testing Cervical

The cobas ® 4800 Human Papillomavirus (HPV) Test is a qualitative in vitro test for the detection of Human Papillomavirus in patient specimens. The test utilizes amplification of target DNA by the Polymerase Chain Reaction (PCR) and nucleic acid hybridization for the detection of 14 high-risk HPV types in a single analysis.

Isothermal Amplification NEB

Isothermal amplification methods provide detection of a nucleic acid target sequence in a streamlined, exponential manner, and are not limited by the constraint of thermal cycling. Although these methods can vary considerably, they all share some features in common.

193130:Gynecologic Pap Test, Liquid-based Preparation and

Liquid-based Pap test; nucleic acid amplification (NAA) (Chlamydia and HPV) References Ferris DG, Wright TC Jr, Litaker MS, et al. Comparison of two tests for detecting carcinogenic HPV in women with Papanicolaou smear reports of ASC-US and LSIL.

Our Technologies – AtilaBiosystems

Omega nucleic acid amplification technology is Atila’s patented isothermal amplification technology which allows the introduction of any artificial sequences during the amplification process. The introduced artificial sequences into the reaction system can be used for many purposes such as signal generation & reaction speed-up.

(PDF) Nucleic Acid Sequence-Based Amplification Assay

This study evaluated the RNA specificity of nucleic acid sequence-based amplification (NASBA)-based HPV detection using HPV DNA plasmids (HPV type

Establishment Registration & Device Listing

1 result found for Establishment Registration or FEI Number :2024800 Owner Operator Number kit, dna detection, human papillomavirus - Cervista HPV HR High-Throughput Automation (HTA); Cervista HPV HR Test Kit(s) nucleic acid amplification assay system, group b streptococcus, direct specimen test - Panther Fusion GBS Assay

cobas® HPV - Diagnostics

The test utilizes amplification of target DNA by the Polymerase Chain Reaction and nucleic acid hybridization for the detection of 14 high-risk HPV types in a single analysis. The test specifically identifies types HPV16 and HPV18 while concurrently detecting the rest of the high risk types (31, 33, 35, 39, 45, 51, 52, 56, 58, 59, 66 and 68).

Nucleic-Acid Amplification Test for STDs

Nucleic-acid amplification tests, also known as NAATs, are used to identify small amounts of DNA or RNA in test samples. They can, therefore, be used to identify bacteria, viruses, and other pathogens even when the material of interest is present in very small amounts. NAATs can even detect a variety of different sexually transmitted diseases (STDs).

DE69430665T2 - Sensitive nucleic acid sandwich

kits nucleic acid hybridization assay sandwich hybridization sensitive nucleic Prior art date C12Q1/6853 — Nucleic acid amplification reactions using modified primers or templates. C Assessment of diseases related to the human papiloma virus. US6207373B1 (en) 1998-02-25:2001-03-27:Nanogen, Inc.

At Home Oral STD Test Kit SelfCollect SelfCollect

SelfCollect’s Oral STD Test Kit for the most common sexually transmitted oral infections. Since many STDs have overlapping symptoms and risk factors, completing an oral STD test kit will give you a broad, cost-effective view of your intimate health.