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2X Taq Master Mix

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産品名稱: 2X Taq Master Mix
産品型號: PLMM01
産品展商: Vivantis Technologies Sdn. Bhd.
美元($)價格: 0.00 元
歐元()價格: 0.00 元
人民幣(¥)價格: 0.00 元
産品文檔: 無相關文檔
發布時間:2020-10-27

簡單介紹

Home DNA Amplification Products 2X Taq Master Mix 2X Taq Master Mix Description 2X Taq Master Mix is an optimized ready-to-use 2X concentrated DNA amplification mixture containing Taq DNA polymerase, reaction buffer, dNTPs and MgCl2. It contains all the components required for routine DNA amplification, except template and primers.


2X Taq Master Mix  的詳細介紹
Home  DNA Amplification Products  2X Taq Master Mix

2X Taq Master Mix

Description
2X Taq Master Mix is an optimized ready-to-use 2X concentrated DNA amplification mixture containing Taq DNA polymerase, reaction buffer, dNTPs and MgCl2. It contains all the components required for routine DNA amplification, except template and primers.

Features

  • Saves time and reduces contamination due to reduced number of pipetting steps.
  • Stable at 4°C for 6 months, allowing immediate reaction setup without the time consuming thawing of reagents.
  • Suitable for all routine DNA amplification applications.

Composition 
Taq DNA Polymerase (0.05u/μl), 2X ViBuffer A (100mM KCl, 20mM TrisHCl (pH9.1 at 20°C) and (0.02% Triton? X-100), 0.4mM dNTPs and 3.0mM MgCl2.

Supplied With

  • 50mM MgCl2
  • Nuclease-free Water

Quality Control 
All preparations are *****ed for contaminating endonuclease, exonuclease, and non-specific DNase activities. Functionally tested in DNA amplification.

Storage & Stability

  • Stable at -20°C for one year or at 4°C for 6 months if properly stored.
  • Stable for 20 freeze-thaw cycles. To avoid frequent freeze-thaw, keeping small aliquots at -20°C is recommended.
  • For daily use, keeping aliquots at 4°C is recommended.

Ordering Information

Catalog No Description Pack Size
PLMM01 2X Taq Master Mix 100 applications

Download
Manual

2X Taq Master Mix

Comparison Test Report

2X Taq Master Mix

Publication
This Product Has Been Used In:
Boonyayatra, S., Tharavichitkut, P., Oliver, S.P. (2018). Virulence-associated genes and molecular typing of Streptococcus uberis associated with bovine mastitis in northern Thailand, Turkish Journal of Veterinary and Animal Sciences, Vol. 42, 73-81 (2018) 
Azhar, N.S., Zin, N.H.M., Abdul-Hamid, T.H.T. (2017). Lactococcus Lactis Strain A5 Producing Nisin-like Bacteriocin Active against Gram Positive and Negative Bacteria, Tropical Life Sciences Research, Vol. 28, No. 2 (2017).
Ajijolakewu, K.A., Leh, C.P., Wan-Abdullah, W.N., Lee, C.K. (2016). Assessment of the Effect of Easily-metabolised Carbon Supplements on Xylanase Production by Newly Isolated Trichoderma asperellum USM SD4 Cultivated on Oil Palm Empty Fruit Bunches. BioResources,Vol. 11, No. 4, 9611-9627 (2016).
Mohamad, Y., Reda, W.W., Abdel-Moein, K., El-Razil, K.A.A., Barakat, A.M.A., El Fadaly, H.A., Hassanain, N.A., Hegazi, A.G. (2016) Prevalence and phylogenetic characterization of Listeria Monocytogenes isolated from processed meat marketed in Egypt.Journal of Genetic Engineering and Biotechnology. 14(1). Pp.119-123
Allahverdi, A., et al. (2015) Differentiation of Human Mesenchymal Stem Cells into Insulin Producing Cells by Using A Lentiviral Vector Carrying PDX1. CELL Journal.17(2), p.231-242. 
Feh, C.F., Wang, K.C., Lu, C.Y., Chiang, L.C., Shieh, D.E., Yen, M.H., Chang, J.S. (2015) Yakammaoto inhibits enterovirus 71 infection by reducing viral attachment, internalization, replication, and translation. Kaohsiung Journal of Medical Sciences. 31. Pp.293-302. 
Sabourmoghaddam, N. Zakaria, M.P., Omar, D. (2015) Evidence for the microbial degradation of imidacloprid in soils of Cameron Highlands. Journal of Saudi Society of Agricultural Sciences.14(2) pp.182-188.
Sabourmoghaddam, N. et al.(2015) Evidence for Microbial Degradation of Imidacloprid in Soils of Cameron Highlands. Journal of Saudi Society of Agricultural Sciences. ScienceDirect. 14(2), p. 182-188. 
Wiparat,S., Poeaim, S., Eiamampai, K., Atittayawan (2015). Gender Identification of Himantopus Himantopus Using PCR-Based Method, International Journal of Agricultural Technology, Chiang Mai Journal of Science, Vol. 11, No.2, 307-314 (2015). 
Belgini, D.R.B., et al (2014) Culturable Bacterial Diversity from a Feed Water of a Reverse Osmosis System, Evaluation of Biofilm Formation and Biocontrol Using Phages. World Journal of Microbiology and Biotechnology. ProQuest. 30, p. 2689-2700.
Belkahia, H., Said, M.B., Hamdi, S.E., Yahiaoui, M., Gharbi, M., Daaloul-Jedidi, M., Mhadbi, M., Jedidi, M., Darghout, M.A., Klabi, I., Zribi, L., Messadi, L. (2014) ) First molecular identification and genetic characterization ofAnaplasma ovis in sheep from Tunisia. Small Ruminant Research. 121. Pp.404-410. 
Dhiritiman, C., Sharma, G.D., Jha, D.K., Hijri, M. (2014). Associations of Arbuscular Mycorrhizal (AM) fungi in the Phytoremediation of Trace Metal (TM) Contaminated Soils, Journal of Research in Biology, Vol. 4, No. 2 (2014).
Reyes, J.C.B., Solon, J.A.A., Rivera, W.L. (2014) The analysis of correlation between IL-1B gene expression and genotyping in multiple sclerosis patients. Microbiology and Infectious Disease 179. Pp..337-341. 
Hipol, R.M. (2012) Molecular Identification and Phylogenetic Affinity of Two Growth Promoting Fungal Endophytes of Sweet Potato (Ipomea batatas (L.) Lam.) from Baguio City, PhilippinesElectric Journal of Biology, 8(3): 57-61.

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