In the biomedical field, the transfer of plasmid vectors into mammalian cells using conventional transfection is the most widely used method. Although a number of more advanced gene introduction vector systems have been developed in recent years (e.g., lentiviral vectors, adenoviral vectors, AAV vectors, and piggyBac, etc.), conventional plasmid gene expression vectors are still used in the majority of laboratories, mainly due to their technical simplicity and efficient transfection rates in various types of cells.
Plasmids are widely used genetic manipulation tools for functional studies of coding genes, microRNAs, lncRNAs, promoter activity, transcription factors and 3'UTR regulation.
Mammalian expression vector construction
Virus vector construction (lentivirus, adenovirus, AAV)
Gene reporter vector construction
Gene mutation
Vector modification
miRNA, lncRNA expression vector construction
Professional technical research team
Rich experience in molecular cloning
Multiple tool vectors are available for various expression systems
Construct different target vectors according to customer's needs
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