Publication | Open Access
A simple and efficient method for direct cloning of PCR products using ddT-tailed vectors
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1991
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EngineeringGeneticsMolecular BiologyNucleic Acid Amplification TestPcr ProductsMolecular GeneticsReal-time Polymerase Chain ReactionLtd16 Gipps St.Test SynthesisPolymerase Chain ReactionCloningGene TransferMolecular Biological MethodDna ReplicationBioinformaticsDirect CloningDdt-tailed VectorsNucleic Acid BiochemistryGenetic EngineeringSynthetic BiologyNucleic Acid AmplificationGene VectorMedicineGenome EditingMolecular Development
Journal Article A simple and efficient method for direct cloning of PCR products using ddT-tailed vectors Get access T.A. Holton, T.A. Holton * Calgene Pacific Pty. Ltd16 Gipps St., Collingwood, Victoria 3066, Australia * To whom correspondence should be addressed Search for other works by this author on: Oxford Academic PubMed Google Scholar M.W. Graham M.W. Graham Calgene Pacific Pty. Ltd16 Gipps St., Collingwood, Victoria 3066, Australia Search for other works by this author on: Oxford Academic PubMed Google Scholar Nucleic Acids Research, Volume 19, Issue 5, 11 March 1991, Page 1156, https://doi.org/10.1093/nar/19.5.1156 Published: 11 March 1991 Article history Accepted: 07 December 1990 Published: 11 March 1991
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