- ￥504
- SBS
- FHTDMD-1 (for 1ml)
- 2026年01月10日
企业认证
相关产品推荐更多 >
万千商家帮你免费找货
0 人在求购买到急需产品
- 详细信息
- 文献和实验
- 技术资料
DNA-Free HS Taq-D 2×SuperMix contains hot-start Taq-D DNA polymerase, dNTPs, and an optimized reaction buffer at a 2× concentration. For DNA amplification, simply add the template, primers, and water to adjust the 2× SuperMix solution to a 1× concentration to proceed with the reaction. The amplification products have an "A" base at the 3' end, making them directly suitable for gene cloning. DNA-Free HS Taq-D 2× SuperMix (dye) contains electrophoresis dye, allowing amplification products to be directly loaded for electrophoresis. If used for cloning, the dye needs to be purified away.
Cat. No.: FHTDMD-1 (for 1ml)
Cat. No.: FHTDMD-5 (for 5ml)
Cat. No.: FHTDMD-20 (for 20ml)
Cat. No.: FHTDMD-50 (for 50ml)
Description
DNA-Free HS Taq-D 2×SuperMix contains hot-start Taq-D DNA polymerase, dNTPs, and an optimized reaction buffer at a 2× concentration. For DNA amplification, simply add the template, primers, and water to adjust the 2× SuperMix solution to a 1× concentration to proceed with the reaction. The amplification products have an "A" base at the 3' end, making them directly suitable for gene cloning. DNA-Free HS Taq-D 2× SuperMix (dye) contains electrophoresis dye, allowing amplification products to be directly loaded for electrophoresis. If used for cloning, the dye needs to be purified away.
Features
- Completely free from bacterial DNA.
- High amplification efficiency.
- Hot-start functionality.
- High product specificity.
- Good stability.
Applications
- Hot-start standard PCR.
- Direct PCR from tissue and blood samples.
风险提示：丁香通仅作为第三方平台，为商家信息发布提供平台空间。用户咨询产品时请注意保护个人信息及财产安全，合理判断，谨慎选购商品，商家和用户对交易行为负责。对于医疗器械类产品，请先查证核实企业经营资质和医疗器械产品注册证情况。
文献和实验Taq-polymerase catalyzed cycle sequencing using fluorescent-labeled dye primers
Each base-specific fluorescent-labeled cycle sequencing reaction routinely included approximately 100 or 200 ng Biomek isolated single-stranded DNA for A and C or G and T reactions, respectively. Double-stranded cycle sequencing
Taq-polymerase catalyzed cycle sequencing using fluorescent-labeled dye terminator reactions
One of the major problems in DNA cycle sequencing is that when fluorescent primers (1) are used the reaction conditions are such that the nested fragment set distribution is highly dependent upon the template concentration
Rapid Separation of Protein‐Bound DNA from Free DNA Using Nitrocellulose Filters
Basic Protocol 1: Materials recipe2× DNA‐binding buffer Double
技术资料暂无技术资料 索取技术资料
