Literature DB >> 23412968

Betaine significantly improves multiplex tetra-primer ARMS-PCR methods.

Bassam Lajin1, Amal Alachkar, Amir Alhaj Sakur.   

Abstract

The tetra-primer ARMS-PCR method offers significant advantages over the commonly used methods to genotype single nucleotide polymorphisms. It offers fast and cost-effective detection and requires minimum level of expertise and basic instrumentation. The benefits of TP-ARMS-PCR increase exponentially upon multiplexing. However, several complications preclude the common use of multiplex TP-ARMS-PCR methods, primarily the lack of robustness and the difficulty of optimization. We have previously developed triplex and quadruplex TP-ARMS-PCR methods involving the simultaneous detection of up to three SNPs in a single reaction and utilized Betaine, a PCR additive used to enable amplification of GC-rich templates with strong secondary structures, in an attempt to facilitate method development and optimization. In the present communication, we introduced experimental data demonstrating the important effects of Betaine on our previous methods and its potential to overcome the ruggedness and robustness issues commonly found in TP-ARMS-PCR methods, and highlighted the general benefits of Betaine with respect to TP-ARMS-PCR. Our data support the routine inclusion of Betaine in all TP-ARMS-PCR methods, especially when multiplexing is concerned.

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Year:  2013        PMID: 23412968     DOI: 10.1007/s12033-013-9651-y

Source DB:  PubMed          Journal:  Mol Biotechnol        ISSN: 1073-6085            Impact factor:   2.695


  11 in total

1.  Competitive amplification and unspecific amplification in polymerase chain reaction with confronting two-pair primers.

Authors:  Nobuyuki Hamajima; Toshiko Saito; Keitaro Matsuo; Kazuo Tajima
Journal:  J Mol Diagn       Date:  2002-05       Impact factor: 5.568

2.  Triplex tetra-primer ARMS-PCR method for the simultaneous detection of MTHFR c.677C>T and c.1298A>C, and MTRR c.66A>G polymorphisms of the folate-homocysteine metabolic pathway.

Authors:  Bassam Lajin; Amal Alachkar; Amir Alhaj Sakur
Journal:  Mol Cell Probes       Date:  2011-11-03       Impact factor: 2.365

3.  A new PCR method: one primer amplification of PCR-CTPP products.

Authors:  Guang Yin; Yoko Mitsuda; Takayuki Ezaki; Nobuyuki Hamajima
Journal:  Mol Biotechnol       Date:  2012-10       Impact factor: 2.695

4.  An efficient procedure for genotyping single nucleotide polymorphisms.

Authors:  S Ye; S Dhillon; X Ke; A R Collins; I N Day
Journal:  Nucleic Acids Res       Date:  2001-09-01       Impact factor: 16.971

5.  Betaine improves the PCR amplification of GC-rich DNA sequences.

Authors:  W Henke; K Herdel; K Jung; D Schnorr; S A Loening
Journal:  Nucleic Acids Res       Date:  1997-10-01       Impact factor: 16.971

6.  Triplex polymerase chain reactions with confronting two-pair primers (PCR-CTPP) for NQO1 C609T, GSTM1 and GSTT1 polymorphisms: a convenient genotyping method.

Authors:  Haruya Kawase; Nobuyuki Hamajima; Akiko Tamakoshi; Kenji Wakai; Toshiko Saito; Kazuo Tajima
Journal:  Asian Pac J Cancer Prev       Date:  2003 Jan-Mar

7.  Multiplex PCR with confronting two-pair primers for CYP1A1 Ile462Val, GSTM1, GSTT1, and NQO1 C609T.

Authors:  Sayo Kawai; Kazuko Nishio; Sakurako Nakamura; Yoshitaka Sekido; Toshimitsu Niwa; Nobuyuki Hamajima
Journal:  Asian Pac J Cancer Prev       Date:  2005 Jul-Sep

8.  Detection of specific polymerase chain reaction product by utilizing the 5'----3' exonuclease activity of Thermus aquaticus DNA polymerase.

Authors:  P M Holland; R D Abramson; R Watson; D H Gelfand
Journal:  Proc Natl Acad Sci U S A       Date:  1991-08-15       Impact factor: 11.205

9.  Betaine can eliminate the base pair composition dependence of DNA melting.

Authors:  W A Rees; T D Yager; J Korte; P H von Hippel
Journal:  Biochemistry       Date:  1993-01-12       Impact factor: 3.162

10.  Polymerase chain reaction with confronting two-pair primers for polymorphism genotyping.

Authors:  N Hamajima; T Saito; K Matsuo; K Kozaki; T Takahashi; K Tajima
Journal:  Jpn J Cancer Res       Date:  2000-09
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  2 in total

1.  Direct and Rapid Identification of Vibrio Cholerae Serogroup and Toxigenicity by a Novel Multiplex Real-Time Assay.

Authors:  Yong Yan; Li Zhan; Guoying Zhu; Junyan Zhang; Ping Li; Lixia Chen; Peiyan He; Jianyong Luo; Zhongwen Chen
Journal:  Pathogens       Date:  2022-07-30

2.  Development of a multiplex PCR assay for the simultaneous and rapid detection of six pathogenic bacteria in poultry.

Authors:  Zhihao Wang; Jiakun Zuo; Jiansen Gong; Jiangang Hu; Wei Jiang; Rongsheng Mi; Yan Huang; Zhaoguo Chen; Vanhnaseng Phouthapane; Kezong Qi; Chen Wang; Xiangan Han
Journal:  AMB Express       Date:  2019-11-14       Impact factor: 3.298

  2 in total

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