Description
General reagent used for long PCR amplification.
Composition
160mM (NH4)2SO4, 500mM Tris-HCl (pH 9.2 at 22°C), 17.5mM MgCl2 and 0.1% Triton™ X-100. The buffer is optimized for use with 0.35mM of each dNTP.
Quality Assurance
Functionally tested in PCR with Taq and Pfu DNA Polymerases. Store at -20°C.
Ordering Information
| Catalog No | Description | Pack Size |
| RB0203 | 10X ViBuffer S | 5x1ml |
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Publication
This Product Has Been Used In:
Nay Yee Wint et al. (2021) A novel nucleic lateral flow assay for screening phaR-containing Bacillus spp., Journal of Microbiology and Biotechnology, 31(1):123-129.
Khalafalla, A.I., Al-Busada, K.A., & El-Sabagh, I.M. (2015)Multiplex PCR for Rapid Diagnosis and Differentiation of Pox and Pox-like Diseases in Dromedary Camels Virology Journal 12(102), p. 1-10.
Nasanit, R., et al (2015) Assesment of Epiphytic Yeast Diversity in Rice (Oryza sativa) Phyllospehere in Thailand by a Culture-independent Approach Antonie van Leeuwenhoek Springer. 107(6), p.1475-1490.
Sezer, C. et al. (2015) Food Handlers: A Bridge in the Journey of Enterotoxigenic MRSA in Food Journal of Consumer Protection and Food Safety,10, p. 123-129.
Sahilah, A.M. et al (2014) Antiobiotic Resistance and Molecular Typing among Cockle (Anadara granosa) Strains of Vibrio parahaemolyticus by Polymerase Chain Reaction (PCR)-based Analysis. World Journal of Microbiology and Biotechnology. ProQuest. 30, p. 649-659.
Sharif, S., et al. (2014) Multiplex PCR in Determination of Opiinae parasitoids of Fruit Flies, Bactrocera sp., Infesting Star Fruit and Guava. Journal of Insect Science. 14(7), p. 1-14.
