Table 1 of Muller, Mol Vis 2007; 13:125-132.


Table 1. γ-Crystallin PCR primers

Shown are the PCR primers for the amplification of genomic canine CRYGB, CRYGC, and CRYGS exons with their flanking intronic regions and PCR primers for the amplification of the cDNA of the canine CRYGB, CRYGC, and CRYGS genes. The asterisk indicates that the forward primer is located 1 bp upstream of the start codon and the reverse primer is located 38 bp downstream of the stop codon. The double asterisk indicates that the forward primer is located 39 bp upstream of the start codon and the reverse primer is located 39 bp downstream of the stop codon. The sharp (hash mark) indicates that the forward primer is located 8 bp upstream of the start codon and the reverse primer is located 90 bp downstream of the stop codon.

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Muller, Mol Vis 2007; 13:125-132 <http://www.molvis.org/molvis/v13/a15/>
©2007 Molecular Vision <http://www.molvis.org/molvis/>
ISSN 1090-0535