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
FAQ
Citations
Documents
| Manual |
|---|
| 11373ES-Manual-Ver.EN20250506_01035b60-2e6e-49d4-8e59-2ae65df37314.pdf |
| MSDS |
|---|
| 11373-MSDS-HB250714.pdf |
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