VERSANT HCV Genotype 2.0 Assay (LiPA)Highly Accurate HCV Genotype and Subtype Detection
The VERSANT® HCV Genotype 2.0 Assay (LiPA)* utilizes the trusted reverse-hybridization technology to detect genotypes 1-6 and subtypes 1a and 1b. This assay is used with the Auto-LiPA 48 and AutoBlot 3000H automated systems to provide highly accurate identification of HCV genotypes and subtypes for optimal patient therapy.
- Proven Reliability
- Total Genotyping Solution
Features & Benefits
Perform HCV Genotyping and Subtyping with Greater Accuracy
The VERSANT HCV Genotype 2.0 Assay (LiPA)* uses the trusted reverse-hybridization technology to provide accurate identification of HCV genotype and subtype specific data for optimal patient therapy.
Subtype Information
- Highly accurate differentiation of subtypes 1a vs.1b showing more than 98% concordance with NS5B sequencing
- Increased genotyping and subtyping accuracy due to dual target analysis of 5’ non coding and core viral genomic regions
Proven Reliability
- Most widely used HCV genotyping assay
- Trusted reverse-hybridization technology (LiPA)
- Validated with NS5B sequencing
Total Genotyping Solution
- Full integration from extraction to automated interpretation
- Minimal hands-on time as most manual steps are automated with the Auto-LiPA 48 or AutoBlot 3000H systems
Customer Testimonial
“The determination of hepatitis C virus (HCV) genotype is mandatory to tailor peginterferon-ribavirin treatment dose and duration. Subtype determination is likely to become useful to tailor specific HCV inhibitor therapy and interpret resistance profiles in the near future. The new VERSANT Genotype Assay (LiPA), a second generation line probe assay, contains probes targeting both the 5’ non coding and the core regions of the viral genome. This has improved the accuracy of HCV genotype 1 subtype determination, particularly discrimination between subtypes 1a and 1b, the most frequent HCV subtypes in clinical practice. The assay also displays improved discrimination among HCV genotypes 1 and 6 relative to the previous version. Only 4% of clinical specimens are mistyped with the VERSANT Genotype Assay relative to the reference method (direct sequence analysis of the NS5B region), which makes it the most accurate method for use in clinical practice. The assay is user-friendly and provides quick results.”
Stèphane Chevaliez
Assistant Hospitalier Universitaire
Centre National de Référence des Hépatites B, C et delta
Laboratoire de Virologie et Inserm U841
Hospital Henri Mondor
Universite Paris XII
94010 CRETEIL, FRANCE