Description
D-Taq PCR Buffer (with MgCl2) combined with D-Taq hot-start enzyme can complete the single and multiple amplification of the target gene fragment, which is suitable for fluorescence quantitative and general PCR. The 10× D-Taq PCR Buffer does not contain Mg2+, dNTP and dUTP, so it needs to be added additionally. In addition, factors that effectively inhibit nonspecific PCR amplification and factors that improve the amplification efficiency of multiple qPCR reactions are added, so that quadruple reactions can be carried out while ensuring the amplification efficiency of primers.
Components
|
Components No. |
Name |
11373ES03 |
|
11373-A |
10× D-Taq PCR Buffer |
1 mL |
|
11373-B |
250 mM MgCl2 |
250 μL |
Storage
This product should be stored at -25~-15℃ for 1 year.
Documents:
Safety Data Sheet
Manuals
Payment & Security
Your payment information is processed securely. We do not store credit card details nor have access to your credit card information.
Inquiry
You may also like
FAQ
The product is for research purposes only and is not intended for therapeutic or diagnostic use in humans or animals. Products and content are protected by patents, trademarks, and copyrights owned by Yeasen Biotechnology. Trademark symbols indicate the country of origin, not necessarily registration in all regions.
Certain applications may require additional third-party intellectual property rights.
Yeasen is dedicated to ethical science, believing our research should address critical questions while ensuring safety and ethical standards.