PCR Enhancer Reference: P021-01 During conventional PCR analysis, DNA fragments with high GC content are often difficult to amplify due to their stable secondary structure. Under ordinary PCR reaction conditions, DNA polymerase is difficult or even impossible to amplify. It can intervene in the secondary structure of high GC content DNA. PCR Enhancer is a mixed additive composed of multiple components, which can effectively reduce the melting temperature of high GC templates and templates with complex secondary structures, and is compatible with almost all DNA polymerase amplification systems. When the optimized PCR program cannot effectively amplify the target fragment, adding PCR Enhancer can often get unexpected results. Application: Increase amplification stability; Improve amplification efficiency
dNTP Mix (10 mM each) Reference: P031-01 This product is an equimolar mixture of high purity dATP, dGTP, dCTP, and dTTP, which can be directly used in PCR, RT (reverse transcription) and one-step RT-PCR experiments.Application: HPLC purity ≥99%; Strict quality control to ensure batch stability
dNTP Mix (10 mM each) Reference: P031-02 This product is an equimolar mixture of high purity dATP, dGTP, dCTP, and dTTP, which can be directly used in PCR, RT (reverse transcription) and one-step RT-PCR experiments.Application: HPLC purity ≥99%; Strict quality control to ensure batch stability
dNTP Mix (2.5 mM each) Reference: P032-01 This product is an equimolar mixture of high purity dATP, dGTP, dCTP, and dTTP, which can be directly used in PCR, RT (reverse transcription) and one-step RT-PCR experiments.Application: HPLC purity ≥99%; Strict quality control to ensure batch stability
dNTP Mix (2.5 mM each) Reference: P032-02 This product is an equimolar mixture of high purity dATP, dGTP, dCTP, and dTTP, which can be directly used in PCR, RT (reverse transcription) and one-step RT-PCR experiments.Application: HPLC purity ≥99%; Strict quality control to ensure batch stability
dUTP (100 mM) Reference: P033-01 These products are high-purity single-component dUTP/dATP/dTTP/dCTP/dGTP, each at a concentration of 100 mM, which can be used for PCR, real-time PCR, RT-PCR, primer extension reaction, DNA sequencing, DNA labeling and other conventional reactions used in molecular biology.Application:
dATP (100 mM) Reference: P034-01 These products are high-purity single-component dUTP/dATP/dTTP/dCTP/dGTP, each at a concentration of 100 mM, which can be used for PCR, real-time PCR, RT-PCR, primer extension reaction, DNA sequencing, DNA labeling and other conventional reactions used in molecular biology.Application:
dTTP (100 mM) Reference: P035-01 These products are high-purity single-component dUTP/dATP/dTTP/dCTP/dGTP, each at a concentration of 100 mM, which can be used for PCR, real-time PCR, RT-PCR, primer extension reaction, DNA sequencing, DNA labeling and other conventional reactions used in molecular biology.Application:
dCTP (100 mM) Reference: P036-01 These products are high-purity single-component dUTP/dATP/dTTP/dCTP/dGTP, each at a concentration of 100 mM, which can be used for PCR, real-time PCR, RT-PCR, primer extension reaction, DNA sequencing, DNA labeling and other conventional reactions used in molecular biology.Application:
dGTP (100 mM) Reference: P037-01 These products are high-purity single-component dUTP/dATP/dTTP/dCTP/dGTP, each at a concentration of 100 mM, which can be used for PCR, real-time PCR, RT-PCR, primer extension reaction, DNA sequencing, DNA labeling and other conventional reactions used in molecular biology.Application:
Heat-labile UDG Reference: P051-01 UDG (Uracil-DNA Glycosylase, uracil-DNA glycosylase) can catalyze the hydrolysis of dU-containing DNA single-stranded or double-stranded uracil base and sugar phosphate backbone N-glycosidic bond, release free uracil, thereby The resulting abasic sites are easily broken by hydrolysis. Heat-labile UDG is derived from psychrophilic marine bacteria and is sensitive to high temperature. It can irreversibly inactivate enzymes above 50℃. It is suitable for PCR/QPCR and RT-PCR/RT-QPCR systems.Application: 55°C 10 min rapid inactivation; Compatible with common PCR reaction systems
Heat-labile UDG Reference: P051-02 UDG (Uracil-DNA Glycosylase, uracil-DNA glycosylase) can catalyze the hydrolysis of dU-containing DNA single-stranded or double-stranded uracil base and sugar phosphate backbone N-glycosidic bond, release free uracil, thereby The resulting abasic sites are easily broken by hydrolysis. Heat-labile UDG is derived from psychrophilic marine bacteria and is sensitive to high temperature. It can irreversibly inactivate enzymes above 50℃. It is suitable for PCR/QPCR and RT-PCR/RT-QPCR systems.Application: 55°C 10 min rapid inactivation; Compatible with common PCR reaction systems