A targeting vector was designed to replace all five exons with the beta-galactosidase cDNA and the neomycin resistance cassette. The neo was subsequently removed via cre mediated recombination. (J:116977)
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A targeting vector was designed to replace all five exons with the beta-galactosidase cDNA and the neomycin resistance cassette. The neo was subsequently removed via cre mediated recombination. (J:116977)