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PCR- and ligation-mediated synthesis of marker cassettes with long flanking homology regions for gene disruption in Saccharomyces cerevisiae.

We developed a novel method for synthesizing marker-disrupted alleles of yeast genes. The first step is PCR amplification of two sequences located upstream and downstream of the reading frame to be disrupted. Due to the addition of non-specific single A overhangs by Taq DNA polymerase, each PCR prod...

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Bibliografische gegevens
Hoofdauteurs: Nikawa, J, Kawabata, M
Formaat: Artigo
Taal:Inglês
Gepubliceerd in: 1998
Onderwerpen:
Online toegang:https://ncbi.nlm.nih.gov/pmc/articles/PMC147308/
https://ncbi.nlm.nih.gov/pubmed/9443982
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