Non-Cloning Ligation
The ability to ligate two or more pieces of DNA together enzymatically has found utility in many applications in the life sciences. Library preparation for Next Generation Sequencing (NGS) typically incorporates a ligation step to add bar-coded adapters to fragmented DNA, a critical step in this popular workflow. Many novel detection methodologies incorporate the ligation of DNA probes followed by a polymerase-based amplification step. For example, single nucleotide polymorphism (SNP) detection using the Ligase Chain Reaction (LCR) is a well-known application using a non-cloning thermostable ligase. Many other detection methods capitalizing on the ligation of DNA are being employed by basic and applied research groups, as well as many molecular diagnostics (MDx) companies.
Choose Type:
- Molecular Cloning Technical Guide
- RNA Ligase Selection Chart
- DNA Ligase Selection Chart
- Troubleshooting Guide for Cloning
- Troubleshooting Tips for Ligation Reactions
- Troubleshooting Guide for Ligases
- Tips for Maximizing Ligation Efficiencies
Brochures
Selection Tools
Troubleshooting Guides
Usage Guidelines
- Anton, B.P., Morgan, R.D., Ezraty, B., Manta, B., Barras, F., Berkmen, M. (2019) Complete genome sequence of Escherichia coli BE104, an MC4100 drivative lacking the methionine reductive pathway Microbiol Resour Announc; 8 (29), e00721-19. PubMedID: 31296691, DOI: 10.1128/MRA.00721-19
- Potapov, V., Ong, J.L., Kucera, R.B., Langhorst, B.W., Bilotti, K., Pryor, J.M., Cantor, E.J., Canton, B., Knight, T.F., Evans, T.C., Lohman, G.J.S. (2018) Comprehensive profiling of four base overhang ligation fidelity by T4 DNA ligase and application to DNA assembly ACS Synth Biol; 7 (11), PubMedID: 30335370, DOI: 10.1021/acssynbio.8b00333
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