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. 2008 Sep 1;39(3):433–437. doi: 10.1590/S1517-83822008000300005

Figure 1.

Figure 1

A) line 1, PCR amplification of chit33 genomic DNA (approximately 1.2 Kb), line 2, digestion of recombinant plasmid containing chit33 gene, using XbaI, (two bands approximately 2.7 and 1.2 Kb), M= DNA size marker; B) line 1, PCR amplification of chit33 cDNA (approximately 1 Kb), line 2, digestion of PCR product using SacI , (two bands approximately o.6 and 0.4 Kb), M= DNA size marker