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Thermolabile Proteinase K is a recombinant Proteinase K engineered for rapid and complete heat inactivation with broad protease activity, for protein and enzyme degradations in nucleic acid preparations and other applications.
Thermolabile Proteinase K is a recombinantly engineered, subtilisin-related serine protease that will hydrolyze a variety of peptide bonds. Unlike other Proteinase K versions that can only be partially inactivated by heat, Thermolabile Proteinase K can be entirely heat-inactivated, allowing for simpler, more efficient workflows, without the need for additional purification steps to remove the enzyme. Thermolabile Proteinase K maintains similar activity and specificity to the wild type version, cleaving peptide bonds at the carboxyl side of most amino acid residues, with some preference at aliphatic or aromatic ones.
Thermolabile Proteinase K (TLPK) can be completely inactivated by incubation at 55°C for 10 minutes, which allows for subsequent enzymatic steps in the same reaction vessel.
Using Thermolabile Proteinase K instead of magnetic beads for cleanup in DNA or RNA library prep keeps the reaction in a single tube, streamlining workflows, improving yield, and reducing costs. This eliminates multiple wash steps, minimizes sample loss, and prevents enzyme carryover between steps. It's especially beneficial for low-input samples, automation, and high-throughput applications.
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