mRNA Therapy

Restriction Enzyme, In Vitro Transcription, post-Transcriptonal modification, Quality Control kits, and CRO Service

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One-stop solution for GMP-grade enzymes and quality control reagents for biopharmaceutical applications

Hzymes mRNA

"mRNA's success highlights its potential in infectious diseases, cancer, and various treatments."

mRNA Material

" Hzymes mRNA Covers drug research emphasizes action modes and processes, materials, tech."

One-stop solution

High-quality Enzymes, Substrates, Kits, and CRO Services for Efficient Drug Development & Production."

Restriction Enzyme

Bsal

BsaI, an IIs restriction endonuclease, is sourced from a modified BsaI gene in E. coli, with native-like specificity and minimized star activity.

BspQl

BspQI can be recombinantly expressed in E. coli that can recognize specific sites and are produced under GMP standards. It is widely used in gene mapping,

RNase Inhibitor

Murine RNase inhibitor is a recombinant murine RNase inhibitor expressed and purified from E.coli. It binds to RNase A, B or C in a 1:1 ratio through non-covalent

Pyrophosphatase Inorganic (yeast)

Pyrophosphatase Inorganic (yeast) is derived from a recombinant E. coli strain carrying Saccharomyces cerevisiae ppa gene.

DNase I

DNase I (deoxyribonuclease I, RNase-free) is derived from a recombinant E. colistrain carrying Bovine Pancreatic DNase I. It is an endonuclease that nonspecifically cleaves DNA

T7 RNA Polymerase(mutants)

T7 RNA Polymerase is a DNA-dependent RNA polymerase from T7 phage ， that possesses a strong and specific 5´→ 3´ RNA polymerase activity.

T7 High Yield RNA Synthesis kit (low dsRNA）

The High-Yield T7 In Vitro Transcription Kit is optimized for transcription reactions using T7 RNA polymerase. It allows for the efficient IVT

NTP Sodium Solution

Each containing a 100 mM aqueous solution of the four essential nucleotide triphosphates (NTPs): ATP, CTP, UTP, and GTP. These high-quality NTP sodium solutions are a fundamental resource

Pseudo UTP Sodium Solution

N1-Me-pUTP or N1-Methyl-Pseudo-UTP, which is a modified nucleotide that can replace the natural cap and is added to in vitro transcription

N1-Me-Pseudo UTP sodium

N1-Me-pUTP or N1-Methyl-Pseudo-UTP, which is a modified nucleotide that can replace the natural cap and is added to in vitro transcription

Cap1 capping system

Capping is a critical quality attribute for mRNA vaccines, as a cap structure at the 5′ end of mRNA is necessary to protect the mRNA molecule from degradation and promote protein translation.

mRNA Cap2'-O- Methyltransferase

mRNA Cap 2´ -O-methyltransferase was derived from a recombinant E. coli strain that carries the gene for the vaccinia mRNA Cap 2´-O-Methyltransferase.

Alkaline Phosphatase

Alkaline Phosphatase is derived from a recombinant E. coli strain that carries the TAB5 gene. The enzyme catalyzes the dephosphorylation of 5´ and 3´ ends of DNA and RNA

Cap1

Critical quality attribute for mRNA vaccines, as a cap structure at the 5′ end of mRNA is necessary to protect the mRNA molecule from degradation

GTP

cell biology and molecular biology research for various applications. GTP is crucial for processes such as RNA transcription, DNA replication,

SAM

An auxiliary substrate involved in methyl transfer reaction. It is synthesized in vivo by adenosine triphosphate

Poly(A) Polymerase

This product is a polymerase expressed by recombinant E.coli. The enzyme does not depend on the template and can catalyze the sequential incorporation of ATP

Vaccinia Capping Enzyme

Vaccinia virus capping enzyme is derived from a recombinant E. coli strain carries the genes for the Vaccinia capping enzyme.

dsRNA ELISA Kit

This kit is an Enzyme-Linked Immunosorbent Assay (ELISA) coupling with biotin-Streptavidin system, for quantitative measurement of dsRNA with length above 60 base..