EBV B95-8 Strain (Type 1) Quantitated Viral DNA
EBVB95-8 quantitated DNA PCR control.
Virus: EBV, B95-8 strain (Type 1)
Virus Preparation: Purified virus
Cell Line for Propagation: B95-8
Suspending Buffer: 10 mM Tris, 1 mM EDTA, pH 8.0
PCR Analysis of DNA Control: PCR analysis was performed on purified EBVB95-8 DNA using the PE Biosystems GeneAmp® Gold PCR Reagent Kit and primers specific to the EBNA-2 gene of EBV. The reaction produced a 170 bp fragment.
DNA Copy Number: 1-2 × 104 copies/µL (varies by lot, please contact ABI for details)
DNA Quantitation: Viral DNA copy number is determined by real time PCR1,2,3 using the Roche LightCycler®. DNA copy number may vary depending on the quantitation method used.
Application: ABI’s quantitated DNA controls are prepared from virus, bacteria, parasites, or mollicutes, and are intended for use as positive PCR quantitation standards for the organism in question. Due to the nature of these products, ABI cannot guarantee their suitability as extraction controls. Additionally, due to the extreme sensitivity of detection in PCR reaction, and since no method of purification can guarantee the complete absence of extraneous agents, DNA controls are not intended for use as negative controls for other organisms.
- 1. "Parallel detection of five human herpes virus DNAs by a set of real-time polymerase chain reactions in a single run." Journal of Clinical Virology. 2003;26(1):85-93.
- 2. "Development of Real-Time PCR Assays for the Quantitative Detection of Epstein-Barr Virus and Cytomegalovirus, Comparison of TaqMan Probes, and Molecular Beacons." J Mol Diagn. 2003;5:15-20.
- 3. "Real-time quantitative PCR of Epstein-Barr virus BZLF1 DNA using the LightCycler." Journal of Virological Methods. 2003;109(2):227-233.
*Note: Upon thawing, centrifuge the vial for a few seconds to remove residual droplets from the lid.



