Simplified template preparation and improved direct sequencing using Taq polymerase.
Author(s) -
Anand Srivastava,
V. Montanaro,
Juha Kere
Publication year - 1992
Publication title -
genome research
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 9.556
H-Index - 297
eISSN - 1549-5469
pISSN - 1088-9051
DOI - 10.1101/gr.1.4.255
Subject(s) - biology , computational biology , taq polymerase , multiple displacement amplification , polymerase chain reaction , dna sequencing , applications of pcr , genetics , digital polymerase chain reaction , dna , thermus aquaticus , dna extraction , gene
A streamlined version of direct dideoxy sequencing is presented that includes template preparation as well as sequencing protocols. The method is used routinely to sequence double-stranded PCR products after minimal purification with one of the primers used in amplification. Either 35S or 32P labeling can be used with equally good results.
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