Fungal-specific PCR primers developed for analysis of the ITS region of environmental DNA extracts
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* Corresponding author: Kendall J Martin kendall@lifetime.oregonstate.edu
BMC Microbiology 2005, 5:28 doi:10.1186/1471-2180-5-28
Figure 3 is incorrectly labeled; the primers were NSI1/58A2R.
Kendall Martin (2007-08-02 17:58) William Paterson University
Figure 3 is incorrectly labeled; the primer pair was not NSI1/NLB4 as stated. These amplifications were performed with the primer pair, NSI1/58A2R. The NSI1/NLB4 product is typically a kilobase or larger.
Competing interests
The commenter is an author of the paper.
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