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At present, PCR technology can be said to be developing rapidly and becoming more and more mature and common, but various problems are still encountered in PCR experiments, such as Ct is too large or has no value, or the amplification efficiency always does not reach the expected 90% -110%, this may be because the primer design is unreasonable or the reaction system needs to be optimized, but it may also be because the sample inhibitor affects the PCR amplification
Flash Robust HotStart DNA Polymerase