mRNA Expression

Scroll Down to Products

Exogenous Gene Expression

Different approaches have been developed to over-express or ectopically express a protein in cells: peptide or full length recombinant protein transfer, viral gene transfer, non-viral DNA transfer and non-viral mRNA transfer. Non-viral mRNA transfer has been around for a long time, but it is not widely used because the expression is transient and generating large amount of mRNA is considered difficult. More recently, the benefits of transient expression, particularly without leaving a footprint in the host genome, have become recognized in many areas of study.

mRNA-mediated ectopic gene expression made a big splash recently through its use for iPSC reprogramming. iPSC factor mRNA enhances iPSC induction efficiency and completely avoids viral integration. This has tremendous implications for clinical use of iPSCs as compared to current methods, because any method involving DNA (e.g. non-integrating lentivirus or minicircle plasmids) presents the risk of random integration by partial recombination. In addition, because mRNA transfection does not require nuclear entry, it is generally easy to do and is not cell cycle-dependent.

RNA can be produced by in vitro transcription (IVT), a simple reaction requiring only a DNA template (double-stranded, or even single-stranded DNA with a double-stranded promoter region), RNA polymerase (from T7, SP6, or T3 phage), NTPs, and a reaction buffer that provides appropriate salt and pH. Using a high quality template; a single 20-50 µl reaction can routinely produce 40-50 µg of mRNA as a single band on an agarose gel from 1 µg of DNA template. At such high concentrations, IVT mRNAs are not nearly as sensitive to RNase-mediated degradation as low-abundance samples.

mRNA transfection has already been developed for use in several applications. Enzymes such as transposase and Cre recombinase have been commonly delivered in the form of mRNA. Other well-known examples of mRNA transfection include loading special cancer antigens or HIV antigens to dendritic cells (DCs) in vitro for personal immunotherapy. PSA antigen expressing DCs transfected by mRNA has moved on to Phase I Clinical Trials for this purpose.

These linear DNA templates are ready to use directly in IVT reactions. Within each template, the coding sequence for a protein is flanked by 5’ and 3’ untranslated regions designed to maximize the translational efficiency and cytoplasmic stability of the mRNA and validated in the iPSC application. The templates drive incorporation of 120-nt polyA tails into RNA transcripts, eliminating the need to enzymatically polyadenylate IVT products before use.

  • 2.5x Nucleotide Mix with Cap Analog

    [[100µl,ABP-PP-NTPMIX]] 2.5x Nucleotide Mix with Cap Analog (ARCA, ATP, GTP, 5m-CTP, Pseudo-UTP) Ready for direct use in IVT reactions. Product Description Download/Print:    Product Protocol/Print: 

    $450.00
    Add to Cart
  • 6F mRNA Reprogramming Premix

    [[50µg,ABP-SC-6FMRNA]] The 6F mRNA reprogramming premix contains all the factors necessary for iPSC generation mixed together in the appropriate ratios.  Each vial contains 50 micrograms of mRNA which is suitable for 8 wells (using a 6...

    $995.00
    Add to Cart