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BioTechniques

Volumn 27, Issue 6, 1999, Pages 1110-1114

Prevention of unexpectedly long PCR products primed at short inverted repeats

(1) Potaman, Vladimir N a,b

a TEXAS A AND M UNIVERSITY SYSTEM (United States)

b TEXAS A AND M HEALTH SCIENCE CENTER (United States)

Author keywords

[No Author keywords available]

Indexed keywords

DNA FRAGMENT;

CLONING VECTOR; DNA SYNTHESIS INHIBITION; DNA TEMPLATE; GENE AMPLIFICATION; PLASMID; POLYMERASE CHAIN REACTION; POLYMERIZATION; REVIEW; TANDEM REPEAT; THERMODYNAMICS;

EID: 0032762236 PISSN: 07366205 EISSN: None Source Type: Journal
DOI: 10.2144/99276bm04 Document Type: Review

Times cited : (2)

References (9)

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2
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- Formation of a combined H-DNA/open TATA box structure in the promoter sequence of the human Na,K-ATPase α2 gene
- Potaman, V.N., D.W. Ussery and R.R. Sinden. 1996. Formation of a combined H-DNA/open TATA box structure in the promoter sequence of the human Na,K-ATPase α2 gene. J. Biol. Chem. 271:13441-13447.
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- Potaman, V.N.¹ Ussery, D.W.² Sinden, R.R.³

3
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- Two-step cycle sequencing reduces premature terminations when using primers with high annealing temperatures
- Prychitko, T.M., E.A. Ries and W.S. Moore. 1998. Two-step cycle sequencing reduces premature terminations when using primers with high annealing temperatures. Mol. Biotechnol. 10:231-236.
- (1998) Mol. Biotechnol. , vol.10 , pp. 231-236
- Prychitko, T.M.¹ Ries, E.A.² Moore, W.S.³

4
- 0032539693
- A unified view of polymer, dumbbell, and oligonucleotide DNA nearest-neighbor thermodynamics
- Santa Lucia, J., Jr. 1998. A unified view of polymer, dumbbell, and oligonucleotide DNA nearest-neighbor thermodynamics. Proc. Natl. Acad. Sci. USA 95:1460-1465.
- (1998) Proc. Natl. Acad. Sci. USA , vol.95 , pp. 1460-1465
- Santa Lucia Jr., J.¹

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- Footprinting protein-DNA complexes in vivo
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- Sasse-Dwight, S.¹ Gralla, J.D.²

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- Occurrence of potential cruciform and H-DNA forming sequences in genomic DNA
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- Schroth, G.P.¹ Ho, P.S.²

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- Molecular mechanisms of mutagenesis by aromatic amines and amides
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8
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- 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
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