Quantitation of DNA Sequences in Environmental PCR Products by a Multiplexed, Bead-Based Method

Author:

Spiro Alexander1,Lowe Mary1

Affiliation:

1. Physics Department, Loyola College in Maryland, Baltimore, Maryland 21210

Abstract

ABSTRACT A first application of a multiplexed, bead-based method is described for determining the abundances of target sequences in an environmental PCR product. Target sequences as little as 0.3% of the total amount of DNA can be quantified. Tests were conducted on 16S ribosomal DNA sequences from microorganisms collected from contaminated groundwater.

Publisher

American Society for Microbiology

Subject

Ecology,Applied Microbiology and Biotechnology,Food Science,Biotechnology

Reference9 articles.

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