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PCR

2X PCR Master mix Solution (i-Taq)

Cat.No Capacity Inquire
25027 0.5 ㎖ x 2 vials Inquire
PRODUCT INFORMATION

 

Description

2x PCR Master mix Solution (i-Taq™) is made from iNtRON’s i-Taq™ DNA Polymerase. i-Taq™ DNA Polymerase included in the product is the 94KDa thermostable DNA polymerase which is expressed in E.coli after cloning the polymerase gene of Thermus aquaticus (strain YT1). This removes protein originated from E.coli and DNA which can affect on PCR as contaminants to perform stable and effective DNA amplification and amplifies to maximum 5 Kb with genomic DNA or cDNA, etc. For the best polymerase activity regardless of the sort of template or the condition of reaction, buffer composition is optimized for the high reproducibility result.

2x PCR Master mix Solution (i-Taq™) is the product what is mixed every component: i-Taq™ DNA Polymerase, dNTP mixture, reaction buffer, and so on- in one tube. This is the product that can get the best result with the most convenience system. The first reason is that it has every components for PCR, so we can do PCR just add a template DNA, primer set, and D.W. The second reason is that it has Gel loading buffer to do electrophoresis, so we can do gel loading without any treatment. In addition, each batches are checked by a thorough Q.C., so its reappearance is high. It is suitable for various sample's experience by fast and simple using method. ​



 

Applications

1) Genomic DNA, cDNA amplify
2) T/A Cloning or Blunt-end Cloning


 

Kit Contents

※ Content : 25027
※ 2x PCR Master mix Solution(i-Taq™) : 0.5 ml x 2 tubes


 

Experimental Informations

1) Comparison test for sensitivity
After the dilution of K562 genomic DNA as per concentration, IL-10(1.3 Kb DNA fragment) PCR was performed for sensitivity test. The result shows that the sensitivity of 2X PCR Master mix Solution (i-Taq™) is equivalent or higher than competitor’s product.




Comparison with 2x PCR Master mix Solution (i-Taq™) and different company solution by amplifying 1Kb DNA fragment from variable amounts of λDNA Aliquots of 5 ㎕ in 20 ㎕ reaction are loaded on 1% agarose gel.





 

Quick Guide





 Citation List

 

1 The Egyptian Journal of Forensic Sciences and Applied Toxicology 2015 Vol.15 Issue 1, pp.1-15  Association of Genetic Polymorphisms of Paraxonase 1 ( Pon1 ) and Glutathione Stransferase ( M1 and T1 ) with Miscarriage in Pesticides Exposed Women at Zagazig University Hospitals  El-Fakharany , Yara M.  |  Arafa , Manar H.  |  Saraya , Yasser S.   Egypt
2 The Egyptian Journal of Aquatic Research
Volume 46, Issue 3, September 2020, Pages 303-309
Occurrence of Penaeus aztecus, Ives, 1891 (Crustacea: Decapoda: Penaeidae) in the coastal water of Alexandria, Egypt Rabab S.El-DeebaMoustafaSarhanbAmal R.KhafageaFatma A.Abdel RazekaMohammedAbdel-WahabbHamdy A.Omara Egypt
3 Biodiversitas Journal of Biological Diversity DNA barcoding of lamp shells (Brachiopoda: Lingula anatina) from Probolinggo, East Java, Indonesia RENI AMBARWATI, DWI A. RAHAYU, FIDA RACHMADIARTI, FIRAS KHALEYLA Indonesia
4 Research J. Pharm. and Tech. 2021; 14(6):3299-3306. Cloning of Acetoacetyl-CoA reductase and Polyhydroxybutyrate synthase genes from the local isolate Bacillus aryabhattai 6N-NRC into E.coli Neveen M. El-Metwally1*, Abd El-Nasser A Egypt
5 Annals of the Romanian Society for Cell Biology, 7853–7865 Molecular Description of Aspergillus Species for Allergies and Asthma Kenan Adnan Abdullah, Milad A. Mezher Iraq
6 All Life, Volume 13, 2020 - Issue 1 The synergistic effect of fenretinide and metformin to achieve a decrease in insulin resistance and inflammatory mediators: an in vivo study Mohamed M.A. Husseina Department Egypt
7 IOP Conference Series: Earth and Environmental Science Microscopical and molecular diagnosis of gastrointestinal nematodes infecting small ruminants in Menofia governorat Ahmed Elkhatam1, Mahmoud R. AbouLaila2, Nasr Elbahy1 and Tamer M. Roshdy3 Malaysia
8 Veterinary Integrative Sciences, (2022). 20(1), 231–245. Molecular detection of Chlamydia spp. and risk factors in farmed siamese crocodile in the mid-northeastern provincial cluster of Thailand Sajana Thapa, Anucha Sirimalaisuwan, Kannika Na Lampang, Veerasak Panyapornwittaya, Warangkhana Chaisowwong Thailand

 

TroubleShooting Guide
QI was using S taq, but recently I am looking for other products because of low sensitivity. We are trying to use it for generic PCR verification without large size. Is there an applicable product?
AWe recommend our i-Taq ™ DNA Polymerase. i-Taq ™ DNA Polymerase is the most basic taq for PCR and you can get satisfactory results in amplification of 1kb or less.
QThe size of the amplified gene is about 4kb. Is it ok to use i-Taq?
AThe recommended maximum amplification of our i-Taq ™ DNA Polymerase is 5kb. In addition, you will get the same efficiency as your i-MAXII ™ for amplification of products below 1kb.
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