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090 _aB-15925
245 1 0 _aA rapid and efficient transformation method for the production of large numbers of transgenic potato plants
490 0 _vPlant Science, 63(1), p.79-85, 1989
520 3 _aA procedure is described for the rapid and efficient production of transgenic potato (Solanum tuberosum L.)plants using Agrobacterium-based vectors. The key factors are the genotype and the level of kanamycin sulfate used for selection. Optimized culture conditions easily and routinely permitted the isolation of hundreds of individual regenerates expressing ß-glucuronidase (GUS)transcriptionally fused to promoters from cauliflower mosaic virus (CaMV 35S)or a class-I patatin gene.
650 1 4 _aCAULIFLOWER MOSAIC VIRUS 35S PROMOTER
650 1 4 _aPATATIN PROMOTER
650 1 4 _aPOTATO
650 1 4 _aTRANSGENIC PLANTS
650 1 4 _aB-GLUCURONIDASE
700 1 2 _aWenzler, H.
700 1 2 _aMignery, G.
700 1 2 _aMay, G.
700 1 2 _aPark, W.
856 4 0 _uhttps://drive.google.com/file/d/1C164gsEC1EHRweo0KFuY8CpMfaa9Brcm/view?usp=drivesdk
_zPara ver el documento ingresa a Google con tu cuenta: @cicy.edu.mx
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