Comparison

TransStart® Taq DNA Polymerase

Item no. TRG-AP141-01
Manufacturer TransGen Biotech
Amount 250 units
Quantity options 250 units 500 units 6 x 500 units 250 units 500 units 6 x 500 units
Category
Type Enzymes
Specific against other
Dry ice Yes
Citations 1 Mi J, Zhou X, Sun R, et al. Disabling spidroin N-terminal homologs' reverse reaction unveils why its intermolecular disulfide bonds have not evolved for 380 million years[J]. International Journal of Biological Macromolecules, 2023.(IF 8.20)
2 Hao T, Xie Z, Wang M, et al. An anaerobic bacterium host system for heterologous expression of natural product biosynthetic gene clusters[J]. Nature communications, 2019.(IF 10.70)
3 Fan Z, Zhao J, Chai X, et al. A Cooperatively Activatable, DNA‐based Fluorescent Reporter for Imaging of Correlated Enzymatic Activities[J]. Angewandte Chemie International Edition, 2021.(IF 15.33)
4 Chi X, Yan R, Zhang J, et al. A neutralizing human antibody binds to the N-terminal domain of the Spike protein of SARS-CoV-2[J]. Science, 2020.(IF 41.00)
ECLASS 10.1 32160410
ECLASS 11.0 32160410
UNSPSC 12352204
Available
Manufacturer - Category
PCR Enzyme
Storage Conditions
at -20 °C for two years
Product Details
TransStart® Taq DNA Polymerase is a hot start Taq DNA polymerase containing Taq DNA polymerase and two proprietary DNA binding proteins. At room temperature, one binding protein binds to double-strand DNA template and another binding protein binds to primer. These unique formulations effectively neutralize the DNA polymerase activity at room temperature. Blocking proteins are released from templates and primers during the initial denaturation. This double blocking method has higher efficiency than antibody based, or chemically modified hot start PCR.


• TransStart® Taq DNA Polymerase offers 18-fold fidelity as compared to EasyTaq® DNA Polymerase.
• Extension rate is about 1-2 kb/min.
• Template-independent “A” can be generated at the 3’ end of the PCR product. PCR products can be directly cloned into pEASY®-T vectors.
• Reduced nonspecific amplification and primer dimer formation.
• Different from Taq antibody, no risk of contamination from mammalian DNA.
• Different from chemical modification, long denaturing step is not needed.
• Amplification of genomic DNA fragment up to 15 kb.


Applications
• Complex templates
• GC/AT-rich templates
• Multiplex PCR
• High yield PCR


Storage
at -20 ℃ for two years


Shipping
Dry ice (-70 ℃)

Note: The presented information and documents (Manual, Product Datasheet, Safety Datasheet and Certificate of Analysis) correspond to our latest update and should serve for orientational purpose only. We do not guarantee the topicality. We would kindly ask you to make a request for specific requirements, if necessary.

All products are intended for research use only (RUO). Not for human, veterinary or therapeutic use.

Amount: 250 units
Available: In stock
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