Production of transgenic mice from DNA-injected embryos cryopreserved by vitrification in microdrops
Jazyk angličtina Země Česko Médium print
Typ dokumentu časopisecké články
PubMed
1597250
Knihovny.cz E-zdroje
- MeSH
- DNA genetika MeSH
- embryo savčí fyziologie MeSH
- erythropoetin genetika MeSH
- exprese genu MeSH
- kryoprezervace * MeSH
- mikroinjekce MeSH
- míra přežití MeSH
- myši inbrední C57BL MeSH
- myši inbrední CBA MeSH
- myši transgenní genetika MeSH
- myši MeSH
- přenos embrya MeSH
- transfekce * MeSH
- zvířata MeSH
- Check Tag
- myši MeSH
- zvířata MeSH
- Publikační typ
- časopisecké články MeSH
- Názvy látek
- DNA MeSH
- erythropoetin MeSH
Transgenic mice were produced from DNA-injected embryos stored for 2 to 30 days in liquid nitrogen. Of the 500 zygotes collected from (C57BL/6 x CBA)F1 mice, 363 (73%) survived DNA injection into pronuclei and 246 (82%) morphologically normal 4- and 8-cell embryos were flushed from temporary recipients 48 h later. Of the 200 DNA-injected 8-cell embryos cryopreserved by vitrification in microdrops, 194 (97%) were recovered and 188 (94%) embryos were intact one hour after thawing. Of the 50 DNA-injected and frozen/thawed embryos, 48 (96%) developed to morulae or blastocysts within 30 h of in vitro culture. Transfer of 100 DNA-injected and cryopreserved 8-cell embryos into 20 day-1 recipients resulted in 47 young born. Two mice were transgenic.