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NGS Library Prep kits

Molecular Research

Drug Discovery

PCR Related Products

55.00
Article number:
P033-01/P034-01/P035-01/P036-01
55.00
Article number:
P033-01/P034-01/P035-01/P036-01
Number of views:
1569
Keywords:
29.00
Article number:
P061
E. coli uracil-DNA glycosylase (UDG) catalyzes the release of uracil from uracil-containing DNA. UDG can effectively hydrolyze uracil on single-stranded or double-stranded DNA, but cannot hydrolyze uracil from oligonucleotides of 6 bases or less.   After strict quality control   Store at -20°C
29.00
Article number:
P061
Number of views:
2240
Keywords:
59.00
Article number:
P051-01/02
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.   55°C 10 min rapid inactivation; Compatible with common PCR reaction systems   Store at -20°C
59.00
Article number:
P051-01/02
Number of views:
2513
Keywords:
Heat-labile UDG
10.10
Article number:
P032-01/02
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.   HPLC purity ≥99%; Strict quality control to ensure batch stability   Store at -20°C
10.10
Article number:
P032-01/02
Number of views:
1865
Keywords:
23.20
Article number:
P031-01/02
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.   HPLC purity ≥99%; Strict quality control to ensure batch stability   Store at -20°C
23.20
Article number:
P031-01/02
Number of views:
2847
Keywords:
12.30
Article number:
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.    Increase amplification stability; Improve amplification efficiency   Store at -20°C
12.30
Article number:
P021-01
Number of views:
2664
Keywords:

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