Saqlain joined ARU in July 2024 as a Lecturer in Biomedical Sciences. He was previously part of the faculty at Brunel University London, developing research in gene therapy. He is passionate about improving gene therapy products, throughout all points of the research pipeline.
Connect with Saqlain on LinkedIn
Saqlain's PhD thesis focused on developing the first human-based in vitro model for assessing genotoxicity of lentiviral vectors. His research has developed to focus on improving gene therapy products through the R&D pipeline including improving viral vector production, purification, and gene transfer, as well as assessing the genotoxicity of viral vectors using an induced pluripotent stem cell-based model.
Saqlain is the Module Lead for Core Biology and is a member of the Biomedical Research Group.
Saqlain is open to discussing potential MSc and PhD projects in the area of gene therapy.
Core Biology (Module Lead)
PhD Cell Biology
BSc (Hons) Biomedical Sciences
Suleman, S., Fawaz, S., Roberts, T., Ellison, S., Bigger, B. and Themis, M. (2024) 'Optimised protocols to generate high titre lentiviral vectors using a novel transfection agent enabling extended HEK293T culture following transient transfection and suspension culture', J Virol Methods, 325, 114884. Available at: https://doi.org/10.1016/j.jviromet.2024.114884. Epub 2024 Jan 11. PMID: 38218417.
Suleman, S., Payne, A., Bowden, J. et al. (2022) 'HIV- 1 lentivirus tethering to the genome is associated with transcription factor binding sites found in genes that favour virus survival', Gene Ther, 29, pp. 720–729. Available at: https://doi.org/10.1038/s41434-022-00335-4
Suleman, S., Schrubaji, K., Filippou, C., Ignatova, S., Hewitson, P., Huddleston, J., Karda, R., Waddington, S. N. and Themis, M. (2021) 'Rapid and inexpensive purification of adenovirus vectors using an optimised aqueous two-phase technology', J Virol Methods, 299, 114305. Available at: https://doi.org/10.1016/j.jviromet.2021.114305. Epub 2021 Oct 6. PMID: 34626684; PMCID: PMC9757833.