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Automated template quantification for DNA sequencing facilities.
Authors:Kathryn M Ivanetich  Wilson Yan  Kathleen M Wunderlich  Jennifer Weston  Ward G Walkup  Christian Simeon
Affiliation:Biomolecular Resource Center, University of California San Francisco, Surge 104, 90 Medical Center Way, San Francisco, CA 94143-0541, USA. kathyi@cgl.ucsf.edu
Abstract:The quantification of plasmid DNA by the PicoGreen dye binding assay has been automated, and the effect of quantification of user-submitted templates on DNA sequence quality in a core laboratory has been assessed. The protocol pipets, mixes and reads standards, blanks and up to 88 unknowns, generates a standard curve, and calculates template concentrations. For pUC19 replicates at five concentrations, coefficients of variance were 0.1, and percent errors were from 1% to 7% (n=198). Standard curves with pUC19 DNA were nonlinear over the 1 to 1733 ng/microL concentration range required to assay the majority (98.7%) of user-submitted templates. Over 35,000 templates have been quantified using the protocol. For 1350 user-submitted plasmids, 87% deviated by >or=20% from the requested concentration (500 ng/microL). Based on data from 418 sequencing reactions, quantification of user-submitted templates was shown to significantly improve DNA sequence quality. The protocol is applicable to all types of double-stranded DNA, is unaffected by primer (1 pmol/microL), and is user modifiable. The protocol takes 30 min, saves 1 h of technical time, and costs approximately $0.20 per unknown.
Keywords:DNA   plasmid   quantification   automation   PicoGreen   core facility
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