Possessing terminal transferase activity! Introducing the research reagents we handle.
"Gene Taq" is a heat-stable DNA polymerase that has been modified from the DNA polymerase gene of Thermus aquaticus YT1, expressed in and purified from E. coli, making it suitable for PCR methods. It possesses terminal transferase activity, allowing the resulting PCR products to be used for TA cloning. Since part of the N-terminal of Taq DNA polymerase has been deleted, it does not have 5' → 3' exonuclease activity. Additionally, it shows particularly high amplification efficiency for DNA fragments under 1 kbp. 【Features】 ■ Particularly high amplification efficiency for DNA fragments under 1 kbp ■ PCR products can be used for TA cloning ■ Part of the N-terminal of Taq DNA polymerase has been deleted *For more details, please refer to the related links or feel free to contact us.
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basic information
【Product Contents (Partial)】 ＜Gene Taq (50 units)＞ ■Components ・Gene Taq ・dNTP Mixture (2.5 mmol/l each) ・10 x Gene Taq Universal Buffer (15 mmol/l Mg2+) *For more details, please refer to the related links or feel free to contact us.
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Applications/Examples of results
【Usage】 ■Standard PCR ■Amplification of low fragments *For more details, please refer to the related links or feel free to contact us.
Company information
Our company is a product development-oriented enterprise that utilizes biotechnology. We develop and manufacture in vitro diagnostic pharmaceuticals (such as pregnancy tests and ovulation tests), diagnostic drugs for environmental, food, and animal and plant diseases, and reagents for genetic engineering research, using our expertise in gene and antibody technology. We hold manufacturing registration and manufacturing and sales licenses for both human and animal products, with over 30 years of experience in the manufacture of in vitro diagnostic pharmaceuticals. Additionally, we are engaged in personalized medicine, advancing research and development of diagnostic drugs using genetic polymorphism analysis and gene expression analysis.