Inhibition of Taq DNA polymerase by iridoid aglycone derivates.
Cellular and molecular biology (Noisy-le-Grand, France), 2012 Fil: García, Celina E..
Pungitore, Carlos Rodolfo +3 more
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Rapid purification of high-activityTaqDNA polymerase
Nucleic Acids Research, 1993 The method described here is derived from that of Engelke et al. (1), and uses the same cloned form of Thermus aquaticus {Taq) DNA polymerase to produce this enzyme in E.coli. The modified purification method described here is quite simple, however it is important to note that factors such as the bacterial strain used, induction time and protein ...
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PCR with Taq DNA Polymerase (M0273) v1
, 2014 This PCR Protocol is for Taq DNA Polymerase with Standard Taq Buffer (M0273)
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Scientific ReportsReverse transcription polymerase chain reaction (RT-PCR) has evolved as a widely used approach in biotechnology and molecular diagnostics. It represents a powerful tool for amplifying and analysing RNA molecules and has therefore found widespread ...
Luisa B. Huber +4 more
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Substitution of Asn for Ser543 in the large fragment of Taq DNA polymerase increases the efficiency of synthesis of long DNA molecules [PDF]
, 1998 Konstantin B. Ignatov +2 more
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Identification of a mutation in the para-sodium channel gene of the cattle tick Rhipicephalus (Boophilus) microplus associated with resistance to synthetic pyrethroid acaricides [PDF]
, 2009 Resistance against synthetic pyrethroid (SP) products for the control of cattle ticks in Australia was detected in the field in 1984, within a very short time of commercial introduction.
Corley, S.W. +5 more
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Taq DNA polymerase slippage mutation rates measured by PCR and quasi-likelihood analysis: (CA/GT)n and (A/T)n microsatellites [PDF]
, 2003 Dheeraj Shinde
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Insertion of the T3 DNA polymerase thioredoxin binding domain enhances the processivity and fidelity of Taq DNA polymerase [PDF]
, 2003 J.F. Davidson
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Improving sensitivity of single tube nested PCR to detect fastidious microorganisms
Heliyon, 2020 Single Tube Nested PCR (ST-nPCR) is of value to clinical laboratories with limited settings for the detection of fastidious microorganisms. The detection sensitivity of ST-nPCR is dependent on ensuring minimal leftovers of outer primers during the second
Diala Shatleh-Rantisi +2 more
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