Modifying Enzymes
Modifying Enzymes
Invitrogen™ T4 DNA Ligase Buffer
T4 DNA Ligase buffer optimizes ligation, which can be performed in 5 minutes
Applied Biosystems™ Exonuclease I, high concentration, (20 units/μL)
Exonuclease I can be used to measure the endonucleolytic cleavage of covalently closed circular single-stranded DNA reacted with an endonuclease of interest.
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™ ezDNase™ Enzyme
SuperScript™ IV VILO™ Master Mix is a reaction master mix designed for fast, sensitive, and reproducible cDNA synthesis in RT-qPCR applications.
Invitrogen™ LR Clonase™ II Plus enzyme
Mix contains a proprietary blend of Int (Integrase), IHF (Integration Host Factor), and Xis (Excisionase) enzymes.
Invitrogen™ S1 Nuclease
Single-strand-specific endonuclease hydrolyzes single-stranded RNA or DNA into 5' mononucleotides
Invitrogen™ Ribonuclease H
Specifically degrades RNA strand of RNA-DNA hybrid to produce 5' phosphate-terminated oligoribonucleotides and single-stranded DNA
Invitrogen™ Ambion™ DNase I (RNase-free)
Nonspecific endonuclease that degrades double- and single-stranded DNA and chromatin
Invitrogen™ Ambion™ RNase I, cloned, 100 U/μL
Efficiently cleaves after all four bases of single-stranded RNA, in contrast to RNase A, which only cleaves after C and U residues
Invitrogen™ TrueCut™ Cas9 Protein v2
A next-generation CRISPR Cas9 protein engineered to deliver maximum editing efficiency.
Thermo Scientific™ T4 DNA Ligase, LC (1 U/μL)
T4 DNA Ligase catalyzes the formation of a phosphodiester bond between juxtaposed 5'-phosphate and 3'-hydroxyl termini in duplex DNA or RNA.
Thermo Scientific™ Modifying Enzymes
Thermo Scientific enzymes for in vitro transcription are designed for efficient and reliable RNA synthesis. These enzymes cover the entire synthesis workflow from template preparation to post-transcriptional modifications, ensuring optimal performance and high yields of synthesized RNA.