Custom IVT mRNA Synthesis
  • Overview
  • Service Features
  • QC Item
  • Case presentation

The expression of exogenous genes in target cells usually requires the introduction of viral or non-viral vectors containing exogenous DNA fragments. In clinical applications, using the traditional methods that direct introduction of exogenous DNA into the human body have certain safety issues. In contrast, in vitro transcribed(IVT) mRNA has natural advantages in safety due to its non infectious ability, unconformity genome and natural degradation in cells. Therefore, it is also a popular tool for gene therapy and new vaccine research.

Advantages

Gene Universal have professional and rich experience technical team for custom IVT mRNA synthesis, now offers one-stop service from Gene synthesis, Plasmid Preparation, linearized plasmid to IVT mRNA synthesis. The length range of IVT mRNA is from 100nt to 5000nt, it can be optimized and customized for different downstream applications, such as template optimization, coding region codon optimization, nucleoside modification, and post transcriptional modification, etc. IVT mRNA can be applied in research fields such as cell transfection, embryo injection, bio-pharmaceuticals, and vaccine development, etc.

Service Features

  • Free codon optimization, improving mRNA translation efficiency

  • Optimized vector, have higher IVT efficiency

  • Custom cap and tail: 5’ cap(Uncapped、Cap0、Cap1) and 3’ PolyA Tail(No Tail、120A Tail, customized), to enhance mRNA stability and translation efficiency

  • Modifications like 5-Methyl-CTP、Pseudo-UTP, which can enhance the mRNA translation efficiency and immune evasion performance

  • Comprehensive quality control plan, customized QC projects according to needs

  • One-stop service from DNA template synthesis to IVT mRNA

  • Rapid delivery – Industry-leading turnaround time

Service Options

Services Step Service Content Turnaround Time Price
1. Gene synthesis, Plasmid Preparation Gene synthesis、Plasmid construction 2-3 weeks Inquiry
Plasmid preparation
2. IVT mRNA Synthesis Linearized plasmid 3-4weeks
IVT, add 5'cap and 3'PolyA tail, modification
3. Quality Control The default QC+extra QC item(Customized) Inquiry

QC Item

QC Item Test Method Specification
Default mRNA Length Agarose gel electrophoresis Expected size band detected
mRNA Sequence Sanger sequencing Correct DNA template
Concentration Nano drop or Qubit 1μg/μl(Default)
Appearance Visual inspect Clear, no visible particles
A260/280 Nano drop 2.0-2.2
Purity HPLC ≥90%
Extra(optional)* Residual DNA template qPCR ≤ 10pg/ug
Endotoxin level Gel-TAL ≤0.005 EU/μg
Residual Protein ELISA or Qubit ≤ 1%
Bioburden Plate 48h sterile spots

* Need Charge extra fee for extra QC items.

Standard Deliverables

  • DNA Sequence verified via

    Sanger sequencing

  • Purity tested by

    gel -electrophoresis

  • Lyophilized mRNA

  • QC report

Case presentation

Agarose gel electrophoresis of mRNA

  • Figure 1. Different length of mRNA

  • Figure 2. 200 nt mRNA

mRNA Purity Test

By use the Linearized plasmid or PCR product as templates, the mRNA Purity>90%

  • Figure 3. Linearized plasmid template:Purity Test of 100 nt mRNA

  • Figure 4. PCR product template:Purity Test of 100 nt mRNA

How to Order?

Submit

Copyright © 2024 Gene Universal, Inc.