FIELD: medicine.
SUBSTANCE: upstream and downstream oligonucleotide primers are used for separating a pol gene fragment of cattle leukaemia provirus. It is followed by electrophoretic measurement of an amplified fragment of the nucleotide sequence. The oligonucleotides of the following structure PF2 are used as primers: 5'-TGA ACG GAC AAA TGG ACT GCT C-3'; PR2: 5'-CCG ACA GAG AGC GAG GAG AG-3', wherein there are found no self-complementary sites inside each primer and between upstream and downstream ones; firing temperature makes 66°C for both oligonucleotides; GC composition is 50% for PF2 and 65% for PR2, and which flank a region of the conservative pol gene of cattle leukaemia virus of size 438 base pairs.
EFFECT: technique is reliable, high-sensitive and high-specific method which can be used to detect an antiviral CLV DNA fragment in a biological material.
3 dwg, 3 tbl, 3 ex
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Authors
Dates
2012-03-20—Published
2010-10-28—Filed