A simple and efficient method for Taq DNA polymerase purification based on heat denaturation and affinity chromatography
Author:
Funder
King Abdullah International Medical Research Center
Publisher
Elsevier BV
Subject
Multidisciplinary
Reference11 articles.
1. A simple and efficient method for extraction of Taq DNA polymerase;Chen;Electron. J. Biotechnol.,2015
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3. 5′ → 3′ exonuclease-based real-time PCR assays for detecting the t(14;18)(q32;21): a survey of 162 malignant lymphomas and reactive specimens;Estalilla;Mod. Pathol.,2000
4. Holland, P.M., et al., 1991. Detection of specific polymerase chain reaction product by utilizing the 5'----3' exonuclease activity of Thermus aquaticus DNA polymerase. In: Proceedings of the National Academy of Sciences, vol. 88(16), pp. 7276-7280.
5. Innis, M.A., et al., 1988. DNA sequencing with Thermus aquaticus DNA polymerase and direct sequencing of polymerase chain reaction-amplified DNA. In: Proceedings of the National Academy of Sciences of the United States of America, vol. 85(24), pp. 9436-9440.
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