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. Author manuscript; available in PMC: 2009 Jun 1.
Published in final edited form as: Nat Protoc. 2007;2(3):577–587. doi: 10.1038/nprot.2007.53

Figure 3.

Figure 3

Distinct banding patterns of DOP-PCR and amino-linking PCR products using long-insert genomic clones as templates. Note the much brighter smears—due to the increased DNA concentration—obtained after the secondary amino-linking PCR (b) compared with primary DOP-PCR (a). Negative controls for both PCRs are running in lanes 16 (a) and 16 (b).