Book section Open Access

Quantitative Real-Time PCR: Fluorescent Probe Options and Issues

Holden, Marcia J.; Wang, Lili


DataCite XML Export

<?xml version='1.0' encoding='utf-8'?>
<resource xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xmlns="http://datacite.org/schema/kernel-4" xsi:schemaLocation="http://datacite.org/schema/kernel-4 http://schema.datacite.org/meta/kernel-4.1/metadata.xsd">
  <identifier identifierType="URL">https://zenodo.org/record/1232956</identifier>
  <creators>
    <creator>
      <creatorName>Holden, Marcia J.</creatorName>
      <givenName>Marcia J.</givenName>
      <familyName>Holden</familyName>
    </creator>
    <creator>
      <creatorName>Wang, Lili</creatorName>
      <givenName>Lili</givenName>
      <familyName>Wang</familyName>
    </creator>
  </creators>
  <titles>
    <title>Quantitative Real-Time PCR: Fluorescent Probe Options and Issues</title>
  </titles>
  <publisher>Zenodo</publisher>
  <publicationYear>2008</publicationYear>
  <dates>
    <date dateType="Issued">2008-03-12</date>
  </dates>
  <resourceType resourceTypeGeneral="Text">Book section</resourceType>
  <alternateIdentifiers>
    <alternateIdentifier alternateIdentifierType="url">https://zenodo.org/record/1232956</alternateIdentifier>
  </alternateIdentifiers>
  <relatedIdentifiers>
    <relatedIdentifier relatedIdentifierType="DOI" relationType="IsIdenticalTo">10.1007/4243_2008_046</relatedIdentifier>
  </relatedIdentifiers>
  <rightsList>
    <rights rightsURI="https://creativecommons.org/publicdomain/zero/1.0/legalcode">Creative Commons Zero v1.0 Universal</rights>
    <rights rightsURI="info:eu-repo/semantics/openAccess">Open Access</rights>
  </rightsList>
  <descriptions>
    <description descriptionType="Abstract">Fluorescence has played a vital role in the development of polymerase chain reaction (PCR)-based DNA amplification. In qualitative PCR, an end point reaction, the amplified DNA, is visualized using DNA intercalating fluorescent dyes. Creative uses of nucleotide probes with fluorescent tags have been developed for real-time quantitative PCR. These probes take advantage of the behavior and properties of fluorophores. There are advantages and disadvantages to various probe types as well as design considerations. Attention to these issues will help in the development of robust and accurate DNA quantification using real-time PCR. Open image in new window</description>
  </descriptions>
</resource>
235
151
views
downloads
Views 235
Downloads 151
Data volume 79.6 MB
Unique views 223
Unique downloads 140

Share

Cite as