Genetic Modification

We leverage advanced genetic modification techniques to provide tailored solutions for your research needs. Whether you're exploring gene function, developing novel therapeutics, or conducting in-depth molecular biology studies, our genetic modification services are designed to accelerate your discoveries.

Genetic modification plays a pivotal role in understanding gene function, unravelling disease mechanisms and developing therapeutic interventions. This field offers a range of techniques to address diverse research needs. 

Advanced techniques to modify genes:

• shRNA (short hairpin RNA): are synthetic RNA molecules designed to induce RNA interference (RNAi). shRNA can be expressed within cells, forming a hairpin structure that is processed into small interfering RNAs leading to their degradation and subsequent gene silencing. Commonly used to create stable cell lines with desired genetic modifications for long-term studies

• siRNA (small interfering RNA): are a class of double-stranded RNA molecules designed to specifically target and degrade complementary mRNA sequences. This mechanism allows for precise and transient gene silencing, making siRNA a valuable tool for functional genomics, drug target validation, and therapeutic development

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