Modifying Enzymes
Invitrogen™ Proteinase K Solution
Proteinase K from the fungus Engyodontium album is a non-specific serine protease that is useful for general digestion of proteins.
Invitrogen™ UltraPure™ Glycogen
Used as carrier for nucleic acid precipitation in ethanol
Thermo Scientific™ Exonuclease III (200 U/μL)
Digest double-stranded DNA or DNA-RNA hybrids with Exonuclease III is a 3'–>5' exonuclease.
Invitrogen™ T4 DNA Ligase (5 U/μL)
Catalyzes the formation of phosphodiester bonds in the presence of ATP between double-stranded DNAs with 3' hydroxyl and 5' phosphate termini
Invitrogen™ SUMO Protease
A recombinant fragment of ULP1 (Ubl-specific protease 1) from Saccharomyces cerevisiae
Invitrogen™ ezDNase™ Enzyme
SuperScript™ IV VILO™ Master Mix is a reaction master mix designed for fast, sensitive, and reproducible cDNA synthesis in RT-qPCR applications.
Applied Biosystems™ Exonuclease I, standard concentration, (10 units/μL)
Exonuclease I is particularly useful in preparing the products of PCR for applications involving sequencing or labeling methods.
Invitrogen™ E. coli DNA Ligase
Catalyzes formation of phosphodiester bonds in presence of β-NAD between double-stranded DNAs with 3' hydroxyl and 5' phosphate cohesive termini
Invitrogen™ L.b. Cas12a Nuclease
L.b. Cas12a Nuclease for simple, quick and specific analysis of your samples.
Invitrogen™ AcTEV™ Protease
Specifically recognizes a seven amino acid sequence (Glu-Asn-Leu-Tyr-Phe-Gln-Gly, cleaving between Gln and Gly), ideal for removing affinity tags from fusion proteins
Invitrogen™ Anza™ T4 PNK Kit
Simplify traditional restriction enzyme cloning with the Invitrogen™ Anza™ Restriction Enzyme Cloning System.
Corning™ Dispase
Bacillus-derived neutral metalloprotease that is recommended for recovering cells cultured on BD Matrigel™ Basement Membrane Matrix
Invitrogen™ T4 DNA Ligase Buffer
T4 DNA Ligase buffer optimizes ligation, which can be performed in 5 minutes
Invitrogen™ Topoisomerase I
Catalyzes removal of superhelical turns from covalently closed DNA by a transient breakage and rejoining of phosphodiester bonds