A diligent and detail-oriented scientist with practical knowledge in molecular biology, cell culture, and analytical methods. Strong experience with laboratory operations, including cell-based assays, primary cell isolation, and working with biologic. Proficient in maintaining high research standards, data integrity, and adherence to SOPs and safety requirements. Experienced in debugging experiments, working in cross-functional teams, and presenting scientific findings. I'm passionate in contributing to cutting-edge immunology and biotherapeutics research.
References available upon request.
The overexpression of Fructose bis Phosphate Aldolase in the C3 cycle was conducted to enhance carbon flux within the rice genome, the gene was introduced into the rice genome through Agrobacterium-mediated transformation.
DNA and RNA extraction to isolate genetic material from transformed plants, and gel electrophoresis to analyze the samples; polymerase chain reaction (PCR) and real-time PCR (qPCR) were utilized for FBPA gene amplification and quantification of gene expression; sodium dodecyl sulfate (SDS) polyacrylamide gel electrophoresis (PAGE) was used for protein separation, followed by immunoblotting to detect the FBPA expression
Phenotypic analysis was carried out to assess the physiological characteristics of the plants, including measurements of plant height and gross weight
Implemented cutting-edge CRISPR-Cas9 technology for precise genetic modifications, utilized Cas9 and sgRNA to disrupt the Met15 gene, inducing targeted double-strand cleavage, and facilitating repair through NHEJ, successfully integrated NatMx gene by co-transforming yeast with pBH750 and pre-cut pMSc-MBB (NatMx), confirmed accurate gene integration using PCR techniques, validated gene integration through Western Blot analysis of NatMx-Myc9 expression, and contributed to advancing genetic engineering capabilities for yeast strains.