FIELD: biotechnology.
SUBSTANCE: following is presented: a method that is implemented by extracting DNA from a sample of biological material, conducting a real-time PCR reaction using a set of oligonucleotide primers and a probe for detecting human herpes virus 6A of the following SEQ ID NO: 1–3 and DNA calibrators with a known concentration, amplification, analysis and interpretation of the results by constructing a calibration line and determining the concentration of target DNA in the test sample. Also a set of oligonucleotide primers and a probe are presented, the said probe has the following nucleotide composition: forward primer HHV-6A/B-for - the following SEQ ID NO: 1; reverse primer HHV-6A/B-rev – the following SEQ ID NO: 2; fluorescent probe HHV-6B-probe – the following SEQ ID NO: 3.
EFFECT: invention can be used in clinical practice and allows to perform 100% specific identification of human herpes virus 6A (HHV-6A) with simultaneous quantitative assessment of the result obtained.
10 cl, 3 tbl, 3 ex
Title | Year | Author | Number |
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METHOD OF QUANTITATIVE DETERMINATION OF DNA OF HUMAN HERPES VIRUS 6A (HHV-6A) AND DNA OF HUMAN HERPES VIRUS 6B (HHV-6B) AND A SET OF OLIGONUCLEOTIDE PRIMERS AND A PROBE FOR ITS IMPLEMENTATION | 2022 |
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Authors
Dates
2023-09-05—Published
2022-12-28—Filed