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5. Quantification of polymerase chain reaction products by affinity-based hybrid collection. Syvänen AC; Bengtström M; Tenhunen J; Söderlund H Nucleic Acids Res; 1988 Dec; 16(23):11327-38. PubMed ID: 2849762 [TBL] [Abstract][Full Text] [Related]
6. Dependence of polymerase chain reaction product inactivation protocols on amplicon length and sequence composition. Espy MJ; Smith TF; Persing DH J Clin Microbiol; 1993 Sep; 31(9):2361-5. PubMed ID: 8408556 [TBL] [Abstract][Full Text] [Related]
7. Optimal activation of isopsoralen to prevent amplicon carryover. Fahle GA; Gill VJ; Fischer SH J Clin Microbiol; 1999 Jan; 37(1):261-2. PubMed ID: 9854109 [TBL] [Abstract][Full Text] [Related]
8. Rapid and reliable protocol for direct sequencing of material amplified by the polymerase chain reaction. Kusukawa N; Uemori T; Asada K; Kato I Biotechniques; 1990 Jul; 9(1):66-8, 70, 72. PubMed ID: 2393575 [TBL] [Abstract][Full Text] [Related]
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12. [Comments on technical problem in PCR]. Oishi N; Sakaki Y Tanpakushitsu Kakusan Koso; 1990 Dec; 35(17):3171-3. PubMed ID: 2287737 [No Abstract] [Full Text] [Related]
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14. Use of UV irradiation to reduce false positivity in polymerase chain reaction. Ou CY; Moore JL; Schochetman G Biotechniques; 1991 Apr; 10(4):442, 444, 446. PubMed ID: 1867851 [TBL] [Abstract][Full Text] [Related]
15. Enzymatic amplification of DNA by PCR: standard procedures and optimization. Kramer MF; Coen DM Curr Protoc Mol Biol; 2001 Nov; Chapter 15():Unit 15.1. PubMed ID: 18265115 [TBL] [Abstract][Full Text] [Related]
16. Use of PCR primers containing a 3'-terminal ribose residue to prevent cross-contamination of amplified sequences. Walder RY; Hayes JR; Walder JA Nucleic Acids Res; 1993 Sep; 21(18):4339-43. PubMed ID: 8414989 [TBL] [Abstract][Full Text] [Related]
17. A general method of polymerase-chain-reaction-enabled protein domain mutagenesis: construction of a human protein S-osteonectin gene. Villarreal XC; Long GL Anal Biochem; 1991 Sep; 197(2):362-7. PubMed ID: 1838462 [TBL] [Abstract][Full Text] [Related]
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