FIELD: biotechnology. SUBSTANCE: method includes the following stages: introduction of gene-engineering construction into an embryo, embryonic cultivation up to blastocyst stage, blastocystic trophoblast biopsy, isolation of total DNA out of a cut-off trophoblast fragment, total DNA microfractioning by a nonsubmarine electrophoresis variant due to sealing the holes with 0.8%-agarose at low temperature of solidification at division to low- and high- molecular fractions, detection of transgenic integration into embryonic genome. EFFECT: increased efficiency of technology in obtaining transgenic animals. 2 tbl
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Authors
Dates
2002-01-20—Published
1999-10-07—Filed