Three yeast artificial chromosome (YAC) libraries were constructed using two human cell lines and the pYAC-RC vector. The main differences from the previously described methods were: i) genomic DNA was digested in low melting point (LMP) agarose blocks with the rare cutting enzyme ClaI; ii) DNA was ligated in melted LMP agarose after agarase treatment; iii) spheroplast regeneration plating was done in calcium alginate thin layer. In addition, a panel of PCR primers was used to identify quickly the presence in the libraries of repetitive and single copy human DNA sequences.

Simplified construction and characterization of yeast artificial chromosome libraries.

VOLINIA, Stefano;PIVA, Maria Roberta;DEL SENNO, Laura
1992

Abstract

Three yeast artificial chromosome (YAC) libraries were constructed using two human cell lines and the pYAC-RC vector. The main differences from the previously described methods were: i) genomic DNA was digested in low melting point (LMP) agarose blocks with the rare cutting enzyme ClaI; ii) DNA was ligated in melted LMP agarose after agarase treatment; iii) spheroplast regeneration plating was done in calcium alginate thin layer. In addition, a panel of PCR primers was used to identify quickly the presence in the libraries of repetitive and single copy human DNA sequences.
1992
Volinia, Stefano; Piva, Maria Roberta; Bozza, A.; Stefani, S.; Gandini, D.; DEL SENNO, Laura
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11392/1682589
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