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CleanAmp™ Publications

Valenti et al.  Naked-eye fingerprinting of single nucleotide polymorphisms on psoriasis patients. Nanoscale, 8, 11027–11033 (2016)

Yoneda et al. Polymicrobial amniotic fluid infection with Mycoplasm/Ureaplasma and other bacteria induces severe intra-amniotic inflammation associated with poor perinatal prognosis in preterm labor.  Am. J. Reprod. Immunol. 1-12 (2015)

Ea et al. Distinct polymer physics principles govern chromatin dynamics in mouse and Drosophila topological domains. BMC Genomics  16:607 (2015)

Ueno et al. Eukaryote-Made Thermostable DNA Polymerase Enables Rapid PCRBased Detection of Mycoplasma, Ureaplasma and Other Bacteria in the Amniotic Fluid of Preterm Labor Cases. PLoS ONE 10(6): e0129032. doi:10.1371/ journal.pone.0129032 (2015)

Brkic Bubola et al. Characterization of Bova Olive Cultivar and Oil Food Technol. Biotechnol. 52 (3) 342–350 (2014)

Xiao X, Zhai J, Zeng J, Tian C, Wu H, Yu Y. Comparative Evaluation of a Triplex Nucleic acid test for Detection of HBV DNA, HCV RNA, and HIV-1 RNA, with the Procleix Tigris System. J Virol Methods. 2012 Nov 8. doi: 10.1016/j.jviromet.2012.10.015.

Shore S, Hidalgo Ashrafi E, Paul N. (2012). Hot Start 7-Deaza-dGTP Improves Sanger Dideoxy Sequencing Data of GC-Rich Targets, DNA Sequencing - Methods and Applications, Dr. Anjana Munshi (Ed.), ISBN: 978-953-51-0564-0, InTech.

Court F, Miro J, Braem C, Lelay-Taha MN, Brisebarre A, Atger F, Gostan T, Weber M, Cathala G, Forné T. Modulated contact frequencies at gene-rich loci support a statistical helix model for mammalian chromatin organization. Genome Biol. 2011;12(5):R42. Epub 2011 May 10.

Shore S, Paul N. Robust PCR amplification of GC-rich targets with Hot Start 7-deaza-dGTP, BioTechniques 2010, 49(5): 841-843.

Paul N, Shum J, Le T. Hot start PCR. Methods Mol Biol. 2010;630:301-18.

Hidalgo Ashrafi E, Yee J, Paul N. Selective control of primer usage in multiplex one-step reverse transcription PCR. BMC Molecular Biology 2009, 10: 113.

Hidalgo Ashrafi, E, Paul N. Heat Activatable Primers for Hot Start Primers for Hot Start PCR and Hot Start One-step RT-PCR - End Point and Real-Time Experiments in Current Protocols in Molecular Biology, Wiley Interscience 2009, 15.9.

Hidalgo Ashrafi E, Paul N. Improved PCR specificity with Hot Start PCR primers. BioTechniques 2009, 47(3): 789-90.

Koukhareva I, Lebedev A. 3’-Protected 2’-Deoxynucleoside 5’-Triphosphates as a Novel Tool for Heat-Triggered Activation of PCR. Analytical Chemistry 2009, 81(12): 4955–4962.

Le T, Hidalgo Ashrafi E, Paul N.  Enhancing multiplex PCR efficiency using Hot Start dNTPs. BioTechniques 2009, 47(5): 972-3.

Le T, Paul N. Improved PCR flexibility with Hot Start dNTPs. BioTechniques 2009, 47(3): 789-90.

Lebedev A. Heat Activatable Primers for Hot Start PCR: Oligonucleotide Synthesis and Basic PCR Set-up in Current Protocols in Nucleic Acid Chemistry, Wiley Interscience 2009, 4.35.

Shum J, Paul N. Chemically modified primers for improved multiplex polymerase chain reaction. Analytical Biochemistry 2009, 388: 266-272.

Koukhareva I, Haoqiang H, Yee J, Shum J, Paul N, Hogrefe RI, Lebedev AV. Heat Activatable 3’-Modified dNTPs: Synthesis and Application for Hot Start PCR. Nucleic Acids Symp Ser (Oxf). 2008;(52):259-60.

Koukhareva I, Huang H, Yee J, Paul N, Hogrefe R, Lebedev A. A new Approach to Improved Hot Start PCR: Nucleoside 5'-Triphosphates with Thermolabile 3'-Protecting Group. Collection Symposium Series 2008, Academy of Sciences of the Czech Republic, 10: 259-263.

Lebedev AV, Paul N, Yee J, Timoshchuk VA, Shum J, Miyagi K, Kellum J, Hogrefe RI, Zon G. Hot start PCR with heat-activatable primers: a novel approach for improved PCR performance. Nucleic Acids Res. 2008 Nov;36(20):e131.

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