Enzymes Products & Reviews

Agilent Endoglycosidases (formerly ProZyme) release oligosaccharides from glycoproteins and some other substrates.

Agilent Exoglycosidases (formerly ProZyme) are glycoside hydrolase enzymes that cleave the glycosidic bonds at the terminal residues.

Agilent Glycosyltransferase (formerly ProZyme) kits are enzymes which are capable of adding terminal monosaccharides to released glycans or intact glycoproteins.

The GoTaq® G2 Hot Start Polymerase and Master Mixes simplify your reaction preparation, bringing you the convenience of room-temperature setup and the specificity of a hot start polymerase.   Ready-to-use Master Mix simplifies reaction setup and allows direct-to-gel loading. The optimized formulation provides amplification of a variety of targets, while eliminating non-specific products, resulting in higher yields and gr…

IdeS Protease is an immunoglobulin-degrading enzyme from Streptococcus pyogenes (IdeS). It is an engineered recombinant protease overexpressed in E. coli that cleaves Immunoglobulin G (IgG) with high specificity at a single site below the hinge region, yielding F(ab’)2 and Fc fragments. The protocol for a standard reaction is to add the IdeS Protease to the IgG sample, add 1 unit of IdeS Protease per 1µg of IgG to be digested…

IdeZ Protease is an immunoglobulin-degrading enzyme from Streptococcus equi subspecies zooepidemicus. It is an engineered recombinant protease overexpressed in E. coli. Like IdeS Protease, IdeZ Protease specifically cleaves IgG molecules below the hinge region to yield F(ab′)2 and Fc fragments. However, IdeZ Protease has significantly improved activity against mouse IgG2a and IgG3 subclasses compared to IdeS Protease.

Inhibits Polymerase Activity at Temperatures below 70°C High conc and glycerol-free formulations

Full-Length Form of Taq DNA Polymerase Manufactured Under cGMP Glycerol-free formulation available Custom formats and formulations

BST-RT Polymerase is ideal for isothermal applications such as LAMP and RT-LAMP for its superior amplification performance and robustness, especially at point-of-care diagnostics

Type III-A, ≥85% RNase A basis (SDS-PAGE), 85-140 Kunitz units/mg protein

The Transcreener dAMP Exonuclease Assay directly measures dAMP produced by exonuclease enzymes as they cleave polynucleotides. 

resDetect™ DNase Activity Assay Kit (Fluorescence) uses the FRET method to detect DNase in buffers, reagents, and other components within 30 minutes. It offers a rapid, sensitive, and quantitative tool for identifying DNase contamination. Additionally, the DNase and RNase Activity Assay Kit enables simultaneous quantitative detection of DNases and RNases in a single assay.

Lysyl Endopeptidase, Mass Spectrometry Grade is a freeze dried product that retained sufficient activity for in-gel digestion and packed in very small quantities for convenience purposes.

Salt Active Nuclease High Quality (SAN HQ) is a Bioprocessing Grade nuclease available in GMP grade developed as the most efficient solution for removal of both single and double stranded DNA and RNA at high salt conditions(400–700 mM). It excels in DNA removal for robust viral vectors like Adenovirus and AAV, ensuring superior product purity while improving DSP. Ideal for gene therapy and vaccine manufacturing. Triton free av…

resDetect™ RNase Activity Assay Kit (Fluorescence) uses the FRET method to detect RNase in buffers, reagents, and other components within 30 minutes. It offers a rapid, sensitive, and quantitative tool for identifying RNase contamination. Additionally, the DNase and RNase Activity Assay Kit enables simultaneous quantitative detection of DNases and RNases in a single sample.

ArcticZymes are the inventors of Shrimp Alkaline Phosphatase (SAP). Including its recombinant version (rSAP), it is the first heat-labile, all-purpose alkaline phosphatase, Unlike other alkaline phosphatases, rSAP can be fully inactivated by a short heat treatment of 15 minutes at 65°C. SAP is the gold-standard DNA modifying enzyme, valued for its convenience and versatility. Available in glycerol-free, lyophilization friendl…

A fast-activating, antibody-free hot-start Taq polymerase formulated for NGS-based high-throughput proximity extension assays (PEA).

ArcticZymes are the inventors of Cod Uracil-DNA Glycosylase (Cod UNG). Developed from Atlantic Cod it is the only commercially available UNG enzyme that is completely and irreversibly inactivated by moderate heat treatment. The enzyme is produced in a recombinant E. coli (ung-) strain that contains a modified Cod UNG gene. Ideal for PCR Carry-Over Prevention and other applications.

ArcticZymes' IsoPol® isothermal polymerases are engineered for rapid, efficient DNA amplification in point-of-care (POC) settings. With enhanced strand displacement, high processivity, and tolerance to biological matrices, they allow faster diagnostics with minimal sample prep. IsoPol BST+ and IsoPol SD+ excel in challenging environments, supporting popular methods like LAMP for quick, reliable results at optimal temperatures.

UltraScript® cDNA Synthesis Kit Separate Oligos contains all the components for efficient and sensitive cDNA synthesis over a broad range of RNA template concentrations. Anchored oligo(dT) and random hexamers are provided separately for user optimisation depending on the type of analysis needed.

The Heat&Run® gDNA removal kit removes contaminating gDNA from RNA prior to RT-qPCR. The kit is based on the recombinant heat labile dsDNase, which is irreversibly inactivated at low temperatures (5 minutes at 58ºC or 15 minutes at 55ºC). Reverse Transcription can be performed in the same tube, thereby minimizing pipetting steps and reducing hands-on time.

UltraScript 2.0 cDNA Synthesis Kit Separate Oligos containins all the components required for fast, reliable and unbiased cDNA synthesis of the most challenging RNA sample types. Anchored oligo(dT) and random hexamers are provided separately for user optimisation depending on the type of analysis needed.

Double-Strand Specific dsDNase from ArcticZymes is ideal for removing contaminating DNA from PCR master mixes, preventing false positives in bacterial typing. Recombinantly produced in Pichia pastoris, it cleaves dsDNA with 5000-fold higher specificity than ssDNA. Easily inactivated by moderate heat (65°C), it allows for direct addition of DNA templates post-cleanup, ensuring accurate PCR results.

SignalChem Biotech (part of Sino Biological) offers a broad range of recombinant protein and lipid Kinases of superior purity and activity to assist the global academic research and drug discovery efforts with the focus on Kinases.

AZtaq™ DNA Polymerase, derived from Thermus aquaticus, is a high-quality, thermostable enzyme ideal for PCR applications. It catalyzes the synthesis of complementary DNA using a primed template and has 5’-3’ exonuclease activity but lacks 3’-5’ proofreading. AZtaq is compatible with dUTP, allowing efficient carry-over contamination removal when used with Cod UNG.