Overview
When HBV virus DNA is extracted from patients in early stage infection or with low virus load (less than 10e2 copies/ml), there is no appropriate DNA concentration procedure and the HBV DNA can usually not be detected by quantitive PCR methods. This client seeks to develop a rapid and effective method to purify and concentrate the DNA of the HBV virus from a patients serum. They are looking for technologies that can deliver ten times DNA concentration of the HBV virus, from serum, i.e., the detection sensibility of the diagnostic kit should be ≥10e2/ml.
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