107 related articles for article (PubMed ID: 24607271)
1. The influence of nucleotide sequence and temperature on the activity of thermostable DNA polymerases.
Montgomery JL; Rejali N; Wittwer CT
J Mol Diagn; 2014 May; 16(3):305-13. PubMed ID: 24607271
[TBL] [Abstract][Full Text] [Related]
2. [Polymerase chain reaction, cold probes and clinical diagnosis].
Haras D; Amoros JP
Sante; 1994; 4(1):43-52. PubMed ID: 7909267
[TBL] [Abstract][Full Text] [Related]
3. Quantitative effects of position and type of single mismatch on single base primer extension.
Wu JH; Hong PY; Liu WT
J Microbiol Methods; 2009 Jun; 77(3):267-75. PubMed ID: 19285527
[TBL] [Abstract][Full Text] [Related]
4. Steady-state and pre-steady-state kinetic analysis of 8-oxo-7,8-dihydroguanosine triphosphate incorporation and extension by replicative and repair DNA polymerases.
Einolf HJ; Schnetz-Boutaud N; Guengerich FP
Biochemistry; 1998 Sep; 37(38):13300-12. PubMed ID: 9748338
[TBL] [Abstract][Full Text] [Related]
5. Capacity of N4-methyl-2'-deoxycytidine 5'-triphosphate to sustain the polymerase chain reaction using various thermostable DNA polymerases.
Flores-Juárez CR; González-Jasso E; Antaramian A; Pless RC
Anal Biochem; 2013 Jul; 438(1):73-81. PubMed ID: 23548504
[TBL] [Abstract][Full Text] [Related]
6. Heterogeneity of primer extension products in asymmetric PCR is due both to cleavage by a structure-specific exo/endonuclease activity of DNA polymerases and to premature stops.
Tombline G; Bellizzi D; Sgaramella V
Proc Natl Acad Sci U S A; 1996 Apr; 93(7):2724-8. PubMed ID: 8610108
[TBL] [Abstract][Full Text] [Related]
7. Minimum GC-rich sequences for overlap extension PCR and primer annealing.
Nakamura M; Suzuki A; Hoshida H; Akada R
Methods Mol Biol; 2014; 1116():165-81. PubMed ID: 24395364
[TBL] [Abstract][Full Text] [Related]
8. Extension of base mispairs by Taq DNA polymerase: implications for single nucleotide discrimination in PCR.
Huang MM; Arnheim N; Goodman MF
Nucleic Acids Res; 1992 Sep; 20(17):4567-73. PubMed ID: 1408758
[TBL] [Abstract][Full Text] [Related]
9. Stopped-flow fluorescence study of precatalytic primer strand base-unstacking transitions in the exonuclease cleft of bacteriophage T4 DNA polymerase.
Otto MR; Bloom LB; Goodman MF; Beechem JM
Biochemistry; 1998 Jul; 37(28):10156-63. PubMed ID: 9665721
[TBL] [Abstract][Full Text] [Related]
10. Cloning, purification, and characterization of a new DNA polymerase from a hyperthermophilic archaeon, Thermococcus sp. NA1.
Kim YJ; Lee HS; Bae SS; Jeon JH; Lim JK; Cho Y; Nam KH; Kang SG; Kim SJ; Kwon ST; Lee JH
J Microbiol Biotechnol; 2007 Jul; 17(7):1090-7. PubMed ID: 18051318
[TBL] [Abstract][Full Text] [Related]
11. The effect of temperature and oligonucleotide primer length on the specificity and efficiency of amplification by the polymerase chain reaction.
Wu DY; Ugozzoli L; Pal BK; Qian J; Wallace RB
DNA Cell Biol; 1991 Apr; 10(3):233-8. PubMed ID: 2012681
[TBL] [Abstract][Full Text] [Related]
12. Optimal conditions to use Pfu exo(-) DNA polymerase for highly efficient ligation-mediated polymerase chain reaction protocols.
Angers M; Cloutier JF; Castonguay A; Drouin R
Nucleic Acids Res; 2001 Aug; 29(16):E83. PubMed ID: 11504891
[TBL] [Abstract][Full Text] [Related]
13. Highly fluorescent 5-(5,6-dimethoxybenzothiazol-2-yl)-2'-deoxyuridine 5'-triphosphate as an efficient substrate for DNA polymerases.
Sato K; Sasaki A; Matsuda A
Chembiochem; 2011 Oct; 12(15):2341-6. PubMed ID: 21887841
[TBL] [Abstract][Full Text] [Related]
14. Primer/template-independent synthesis of poly d(A-T) by Taq polymerase.
Hanaki K; Odawara T; Muramatsu T; Kuchino Y; Masuda M; Yamamoto K; Nozaki C; Mizuno K; Yoshikura H
Biochem Biophys Res Commun; 1997 Sep; 238(1):113-8. PubMed ID: 9299462
[TBL] [Abstract][Full Text] [Related]
15. Evaluation of 15 polymerases and phosphorothioate primer modification for detection of UV-induced C:G to T:A mutations by allele-specific PCR.
Gale JM; Tafoya GB
Photochem Photobiol; 2004 May; 79(5):461-9. PubMed ID: 15191056
[TBL] [Abstract][Full Text] [Related]
16. Recognition of sequence-directed DNA structure by the Klenow fragment of DNA polymerase I.
Carver TE; Millar DP
Biochemistry; 1998 Feb; 37(7):1898-904. PubMed ID: 9485315
[TBL] [Abstract][Full Text] [Related]
17. Influence of PCR reagents on DNA polymerase extension rates measured on real-time PCR instruments.
Montgomery JL; Wittwer CT
Clin Chem; 2014 Feb; 60(2):334-40. PubMed ID: 24081987
[TBL] [Abstract][Full Text] [Related]
18. Transcription and reverse transcription of artificial nucleic acids involving backbone modification by template-directed DNA polymerase reactions.
Kuwahara M; Takeshima H; Nagashima J; Minezaki S; Ozaki H; Sawai H
Bioorg Med Chem; 2009 Jun; 17(11):3782-8. PubMed ID: 19427792
[TBL] [Abstract][Full Text] [Related]
19. Stopped-flow DNA polymerase assay by continuous monitoring of dNTP incorporation by fluorescence.
Montgomery JL; Rejali N; Wittwer CT
Anal Biochem; 2013 Oct; 441(2):133-9. PubMed ID: 23872003
[TBL] [Abstract][Full Text] [Related]
20. Determination of the reopening temperature of a DNA hairpin structure in vitro.
Pan X
Eur J Biochem; 2004 Sep; 271(18):3665-70. PubMed ID: 15355343
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]