Modifying Enzymes

Modifying Enzymes

Enzymes that structurally alter macromolecules while retaining their own molecular structures. Various modifying enzymes, enzyme mixes, kits, buffers, etc. are available in multiple quantities and concentrations tailored to molecular biology procedures.
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: 50 to 375 U/μL. : Wet Ice. : DNase. : 20,000 U.
: 5 U/μL. : DNA Ligase. : 10X T4 DNA Ligase Buffer. : T4 DNA Ligase.
: Dry Ice. : DNase. : Reaction Buffer. : 50 Reactions.
: Proteinase K. : Liquid.
: 5 U/μL. : Dry Ice. : Ligase. : 5X Reaction Buffer.
: 1 U/μL. : DNase. : Reaction Buffer. : 1,000 units.
: Dry Ice. : LR Clonase. : Enzyme Buffer. : LR Clonase Enzyme Mix.
: DNase-Free, RNase-Free. : Chromatin Biology/RNA Extraction/DNA Extraction. : Wet Ice. : 5 mL.
: Dry Ice. : LR Clonase. : Reaction Buffer. : LR Clonase Enzyme.
: Dry Ice. : BP Clonase. : Enzyme Buffer. : BP Clonase Enzyme Mix.
: T. album : Bottle. : Dry Ice. : Proteinase K.
: 50 U/μL. : Transparent. : ≥95%. : 7.1 to 7.9
: 50 U/μL. : DNase. : Reaction Buffer. : 1,000 units.
: 10X. : RT-qPCR. : On dry ice. : DNase.
: 20 mg/mL. : DNase-Free, RNase-Free. : Chromatin Biology/RNA Extraction/DNA Extraction. : Approved for shipment on Wet or Dry Ice.
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Alkaline phosphatase and polynucleotide kinase for DNA and RNA dephosphorylation or phosphorylation., Properties of RNA polymerases for in vitro transcription, RNA labeling, synthesis of antisense RNA and siRNA, studies of RNA splicing and secondary structure.
We offer an extensive portfolio of Thermo Scientific restriction enzymes and modifying enzymes including DNA and RNA polymerases, phosphatases, kinases, and nucleases. Whatever your downstream applications are, it is critical to use reliable, high-quality, high-purity reagents in your experiments.
Documents & Support (991)
Are the Anza modifying enzymes compatible with the Anza Buffer?
I would like to perform a restriction enzyme double digestion. Do you offer a tool to determine optimal reaction conditions?