ISSNs: , 1940-9818

References in BioTechniques:

Title Authors Year
Producing single-stranded DNA probes with the Taq DNA polymerase: a high yield protocol. Finckh U, Lingenfelter PA, Myerson D 1991
Enhancement of PCR amplification yield and specificity using AmpliTaq Gold DNA polymerase. Moretti T, Koons B, Budowle B 1998
Single-step purification of a thermostable DNA polymerase expressed in Escherichia coli. Desai UJ, Pfaffle PK 1995
Site-directed mutagenesis using Pfu DNA polymerase and T4 DNA ligase. Adereth Y, Champion KJ, Hsu T, Dammai V 2005
Specific inhibition of PCR by non-extendable oligonucleotides using a 5' to 3' exonuclease-deficient DNA polymerase. Yu D, Mukai M, Liu Q, Steinman CR 1997
Purification of a thermostable DNA polymerase from Thermus thermophilus HB8, useful in the polymerase chain reaction. Carballeira N, Nazabal M, Brito J, Garcia O 1990
Extended stability of Taq DNA polymerase and T4 DNA ligase at various temperatures. Youngblom J 2003
Polyelectrolyte surface interface for single-molecule fluorescence studies of DNA polymerase. Kartalov EP, Unger MA, Quake SR 2003
TempliPhi, phi29 DNA polymerase based rolling circle amplification of templates for DNA sequencing. Nelson JR, Cai YC, Giesler TL, Farchaus JW, Sundaram ST, Ortiz-Rivera M, Hosta LP, Hewitt PL, Mamone JA, Palaniappan C, Fuller CW 2002
Use of the restriction enzyme AvaI and exo- Bst polymerase in strand displacement amplification. Milla MA, Spears PA, Pearson RE, Walker GT 1998
Cycle sequencing protocol using deep VentR (exo-) DNA polymerase and reduced dNTP and [alpha-35S]dATP concentrations. Mariamé B 1996
CircumVent thermal cycle sequencing and alternative manual and automated DNA sequencing protocols using the highly thermostable VentR (exo-) DNA polymerase. Sears LE, Moran LS, Kissinger C, Creasey T, Perry-O'Keefe H, Roskey M, Sutherland E, Slatko BE 1992
Generation of genomic mini-libraries by Taq DNA polymerase modification of genomic fragments. Huang HJ, Pears C 1998
Addendum: Site-directed mutagenesis using Pfu DNA polymerase and T4 DNA ligase. 2005
Primer-directed mutagenesis of an intact plasmid by using Pwo DNA polymerase in long distance inverse PCR. Hidajat R, McNicol P 1997
Bst DNA polymerase permits rapid sequence analysis from nanogram amounts of template. Mead DA, McClary JA, Luckey JA, Kostichka AJ, Witney FR, Smith LM 1991
Specific terminal labeling of DNA molecules. Shigemori Y, Oishi M 2007
DNA sequencing with delta Taq DNA polymerase. Ranu RS 1995
Incorporation of reporter-labeled nucleotides by DNA polymerases. Anderson JP, Angerer B, Loeb LA 2005
Comparable sensitivity and specificity of nested PCR and single-stage PCR using a thermally activated DNA polymerase. Zimmermann K, Mannhalter JW 1998
Direct cloning of PCR products amplified with Pwo DNA polymerase. Hinnisdaels S, Del-Favero J, Vauterin M 1996
Direct radioactive labeling of unpurified PCR products using Klenow fragment. McDaniel TK, Huang Y, Yin J, Needleman SW, Meltzer SJ 1991
Organic solvents as facilitators of polymerase chain reaction. Pomp D, Medrano JF 1991
Quality control PCR: a method for detecting inhibitors of Taq DNA polymerase. Reiss RA, Rutz B 1999
In vitro production and screening of DNA polymerase eta mutants for catalytic diversity. Glick E, Anderson JP, Loeb LA 2002
Utility and accuracy of template-directed dye-terminator incorporation with fluorescence-polarization detection for genotyping single nucleotide polymorphisms. Akula N, Chen YS, Hennessy K, Schulze TG, Singh G, McMahon FJ 2002
Advantages of a new Taq DNA polymerase in multiplex PCR and time-release PCR. Kebelmann-Betzing C, Seeger K, Dragon S, Schmitt G, Möricke A, Schild TA, Henze G, Beyermann B 1998
Post-PCR labeling using Taq DNA polymerase. Chen Z, Ruffner DE 1997
Gene walking by PCR amplification of short fragments from Taq DNA polymerase--modified P1 plasmid DNA and TA cloning. Baury B, Masson D, Lustenberger P, Denis MG 1999
Heat-mediated activation of affinity-immobilized Taq DNA polymerase. Nilsson J, Bosnes M, Larsen F, Nygren PA, Uhlén M, Lundeberg J 1997
Thermo Sequenase DNA polymerase and T. acidophilum pyrophosphatase: new thermostable enzymes for DNA sequencing. Vander Horn PB, Davis MC, Cunniff JJ, Ruan C, McArdle BF, Samols SB, Szasz J, Hu G, Hujer KM, Domke ST, Brummet SR, Moffett RB, Fuller CW 1997
Comparison between Taq DNA polymerase and its Stoffel fragment for quantitative real-time PCR with hybridization probes. Wilhelm J, Pingoud A, Hahn M 2001
TaqStart Antibody: "hot start" PCR facilitated by a neutralizing monoclonal antibody directed against Taq DNA polymerase. Kellogg DE, Rybalkin I, Chen S, Mukhamedova N, Vlasik T, Siebert PD, Chenchik A 1994
A functional assay for Taq DNA polymerase in PCR. Wada M, Klein C, Schell J, Reiss B 1994
A biological method for examining the effect of codon changes in a conserved region of DNA polymerase. DeFilippes FM 1994
Reducing the impact of PCR-mediated recombination in molecular evolution and environmental studies using a new-generation high-fidelity DNA polymerase. Lahr DJ, Katz LA 2009
Large fragment of DNA polymerase I from Bacillus stearothermophilus (Bst polymerase) is stable at ambient temperature. Lu YY, Ye SY, Hong GF 1991
Fluorometric assay for DNA polymerases and reverse transcriptase. Seville M, West AB, Cull MG, McHenry CS 1996
DNA sequencing with [alpha-33P]-labeled ddNTP terminators: a new approach to DNA sequencing with Thermo Sequenase DNA polymerase. Fan J, Ranu RS, Smith C, Ruan C, Fuller CW 1996
Reducing "double sequences" in automated DNA sequencing with T7 DNA polymerase and internal labeling. Wiemann S, Schilke A, Rechmann S, Zimmermann J, Voss H, Ansorge W 1996
Nonradioactive detection of retroviral-associated RNase H activity in a microplate-based, high-throughput format. McLellan N, Wei X, Marchand B, Wainberg MA, Götte M 2002
Reverse transcription slippage over the mRNA secondary structure of the LIP1 gene. Zhang YJ, Pan HY, Gao SJ 2001
Simultaneous multiple target detection in real-time loop-mediated isothermal amplification. Tanner NA, Zhang Y, Evans TC 2012
High-temperature, nonradioactive primer extension assay for determination of a transcription-initiation site. Yamada M, Izu H, Nitta T, Kurihara K, Sakurai T 1998
Fast mitochondrial DNA isolation from mammalian cells for next-generation sequencing. Quispe-Tintaya W, White RR, Popov VN, Vijg J, Maslov AY 2013

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