Damiani G, Pilla F, Leone P, Cacciò S
Istituto per la Difesa e la Valorizzazione del Germoplasma Animale, CNR, Milano, Italy.
Anim Genet. 1992;23(6):561-5. doi: 10.1111/j.1365-2052.1992.tb00180.x.
We have used the polymerase chain reaction (PCR) to amplify exon VII of the bovine beta-casein gene. The mutations responsible for the B variant were identified by direct sequencing of the amplification products. A bidirectional allele-specific PCR method (BAS-PCR) has been developed using oligonucleotides overlapping the mutation site at their 3' ends. This new procedure allows a rapid and reliable discrimination between the B and non-B alleles of beta-casein.