AAV

Find optimized AAV vectors for efficient gene delivery for efficient in vivo and in vitro research applications.

MBP AAV vector systems are designed for gene therapy research, targeted gene expression,  and disease modeling. These vectors are widely used in transgene delivery, gene editing workflows like CRISPR-Cas 9, and long-term expression studies where consistent performance and low immunogenicity are critical. AAV systems support research across oncology, stem cell biology, neuroscience, and molecular therapeutics.

What you will find:

•   Over-Expression AAV Vectors:  Control and reporter vectors, Cre-inducible (DIO) expression systems, control vectors of miRNA, siRNA, and CRISPR/Cas9 for gene expression control, validation, and pathway analysis.
•   Purification & Packaging Kits: for diverse serotypes (1–6), high-titer serotype kits, serotype-specific packaging, transduction enhancers for enhanced delivery efficiency and consistent production of viral vectors.

MBP AAV vectors are purpose-built for functional genomics research and efficient gene therapy. These vectors are designed for high transduction efficiency, reproducible gene expression, and reliable performance across diverse molecular research applications. 

Contact the expert team of MBP today and book reliable AAV vectors for your lab.