In Vitro Transcribed mRNA Services
mRNA Drug Development Services
Plasmid Production For mRNA Synthesis

Plasmid Production For mRNA Synthesis

Seattle Genova's Plasmid DNA Preparation Service is accommodating to both small research labs in addition to large-scale manufacturing biotech and pharmaceutical companies, presenting you with excessive first-class plasmids with 100% full insert sequence accuracy. Choose from a number of our applications that will help you obtain tremendously efficient molecular transfection, and to guide your mRNA development, antibody production, and different preclinical research projects. Plasmids are circular molecules of DNA discovered evidently in bacteria. They replicate independently of the bacterial genomic DNA, assets that make them perfectly suited as a vector for genetic engineering. Purified pDNA may be used as a raw material in techniques which includes the manufacturing of adeno-associated (AAV) and lentiviral vectors, in vitro transcription (IVT) reactions during mRNA production, and direct gene transfer.


A restriction enzyme is a DNA-slicing enzyme that recognizes a selected target sequence and cuts DNA into fragments at or close to that site. Many restriction enzymes produce cut ends with short, single-stranded overhangs. If molecules have matching overhangs, they are able to base-pair and stick together. However, they may not integrate to shape an unbroken DNA molecule till they may be joined through DNA ligase, which seals gaps in the DNA backbone. Plasmids and desired DNA can be added into bacteria through a method referred to as transformation. During transformation, prepared bacterial cells are given a heat shock that encourages them to absorb foreign DNA. Bacteria will multiply and not all colonies will always incorporate the desired plasmid. That is because, throughout a ligation, DNA fragments do not usually get “pasted” in precisely the manner we intend. Instead, we need to acquire DNA from numerous colonies and spot whether or not everyone incorporates the desired plasmid. Methods like restriction enzyme digestion and PCR are commonly used to check the plasmids.




Customized plasmid with desired DNA fragment.

A complete work report.


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