Browse our collection of recombinant enzymes — including proteases, kinases, phosphatases, and metabolic enzymes. Each enzyme is produced with high purity and verified enzymatic activity, supporting applications in drug target screening, biochemical pathway analysis, and structural biology. Available in His-tagged and tag-free formats. All products are designated Research Use Only (RUO) — not intended for diagnostic or therapeutic procedures. RUO
Mammalian cells
Beta-Hexosaminidase B (HEXB) is expressed in Mammalian.
Beta-Hexosaminidase B can release all types of GlcNAc(β1-x) units, including the bisecting GlcNAc structure in N-linked glycans.
Homo sapiens (Human)
E. coli
TEV Protease is cloned from Tobacco etch virus (TEV) and expressed in E.coli.
TEV Protease is a highly specific cysteine protease. The TEV Protease recognition sequence with the highest catalytic efficiency is ENLYFQ↓(S/G/A/M/C/H).
E. coli
Benzonase Nuclease is cloned from Serratia marcescens and expressed in E.coli.
E. coli
T5 Exonuclease is cloned from Escherichia phage T5 and expressed in E.coli.
E. coli
Endo S2/Endo-beta-N-acetylglucosaminidase is cloned from Streptococcus pyogenes and expressed in E.coli.
Endo S2 hydrolyses N-linked glycans on IgG and α1-acid glycoprotein.
Mammalian cells
CU43 Protease is cloned from Corynebacterium ulcerans and expressed in Mammalian cells.
Proteomics
E. coli
CU43 Protease is cloned from Corynebacterium ulcerans and expressed in E. coli.
Proteomics
E. coli
CAT / Catalase is cloned from human cell lines and expressed in E.coli.
Proteomics
E. coli
PNGase F is cloned from Elizabethkingia miricola and expressed in E.coli.
Removal of high mannose N-glycans from glycoproteins
E. coli
M-MLV is cloned from MoMLV and expressed in E.coli.
cDNA Synthesis, Reverse Transcription (cDNA Synthesis), RT-PCR & cDNA Synthesis, RT-qPCR, RT-PCR and cDNA Synthesis, PCR