Cloning and characterization of a cDNA e
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Colette Jako; Bernard Teyssendier Serve
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Article
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1996
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Springer
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English
⚖ 388 KB
The cloning of small GTP-binding proteins from Petunia hybrida was performed using a PCR-based strategy. Degenerate primers were designed from the DTAGQE and FMETSA consensus sequences. Three different cDNAs were amplified. The deduced polypeptide sequences PhPCRGP1 and PhPCRGP2 were homologous to R