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Mature mRNA in eukaryotes carries a unique 5′ cap structure (m⁷GpppN), known as the methylguanosine cap, which is essential for translation initiation, protection from RNase degradation, and enhancement of mRNA stability during splicing and nuclear export.

Vaccinia Capping Enzyme GMP-grade (VCE), developed in-house by Biori Biotech, integrates the three enzymatic activities required for capping: RNA triphosphatase, guanylyltransferase, and guanine-N7-methyltransferase.

In the presence of S-adenosylmethionine (SAM) as a methyl donor and guanosine triphosphate (GTP), VCE directly and efficiently adds an m⁷G cap to the 5′ end of mRNA in the correct orientation, producing Cap0-capped RNA with up to 100% capping efficiency in a single reaction.

Vaccinia Capping Enzyme GMP-grade, GMP-BP-E05

USD
$0.00
Features
  • Integrates RNA triphosphatase, guanylyltransferase, and guanine-N7-methyltransferase activities in one enzyme
  • Directly adds an m⁷G cap to the 5′ end of mRNA in the correct orientation
  • Produces Cap0-capped RNA with up to 100% capping efficiency in a single reaction
  • Compatible with GTP and SAM-mediated enzymatic capping workflows
  • Developed in-house by Biori Biotech
  • Cap1 RNA can be obtained by combining with 2′-O-Methyltransferase GMP-grade (GMP-BP-E06)
  • Cap 0 capping of mRNA for in vitro or in vivo translation
  • Generation of Cap1 RNA when used in combination with 2′-O-Methyltransferase GMP-grade (GMP-BP-E06)
Component GMP-BP-E05-1K GMP-BP-E05-10K GMP-BP-E05-100K
Vaccinia Capping Enzyme GMP-grade (10 U/µL) 1,000 U / 0.1 mL 10,000 U / 1 mL 100,000 U / 10 mL
10× Capping Buffer 0.2 mL 2 mL 20 mL
GTP Solution (10 mM) 0.1 mL 1 mL 10 mL
SAM (32 mM) 20 µL 0.2 mL 2 mL
Condition Recommendation
Storage Store at −20 ± 5 °C.
Handling Mix gently before use. Avoid repeated freeze-thaw cycles.
Capping Buffer 500 mM Tris-HCl (pH 8.0), 50 mM KCl, 10 mM MgCl₂, 10 mM DTT
Storage Buffer 20 mM Tris-HCl (pH 8.0), 100 mM NaCl, 1 mM DTT, 0.1 mM EDTA, 0.1% (v/v) Triton X-100, 50% (v/v) glycerol

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