Highly motivated, hard-working, and diligent stem cell biologist with 10+ years of experience in stem cell research with a goal to advance a career in the field of regenerative medicine. Expertise in hPSC/iPSC culture, differentiation, and in vivo approaches. Over 10 years of experience working with several cancer cell lines, primary cell lines, and mouse model systems. Involved in studies to develop in vitro and in vivo approaches to study liver, cardiovascular, hematopoietic progenitors. Worked on dynamic collaborative projects and demonstrated ability at independent planning, execution, and analysis of experiments. Organized and meticulous with good oral and written communication skills.
· Differentiated hPSC (H9) into early endoderm progenitors and hepatocytes (2D) in feeder-free conditions and characterized them by qPCR, flow cytometry, and immunofluorescence.
· Analysis of adult and embryonic mouse liver progenitors’ and organoids upon injury, and drug administration methods by immunofluorescence (confocal), qPCR, flow cytometry and lineage tracing.
· Analysis of mouse and human liver/ bone marrow single-cell RNA seq studies[AV1] using R.
· Analysis of absence of TIMPs on hematopoietic development using multiple approaches like primary/secondary transplant, reverse transplant and assaying them by flow cytometry.
· Generation and analysis of manipulated hPSCs using CRISPR/Cas9 gene editing system.
· Analysis of genetically modulated HR+ and HR- [AV1] breast cancer cell lines using lentiviral vectors and analyzed EMT and EMT-associated changes in them by immunofluorescence, qPCR, migration, and proliferation assays.
· Analyzed the effect of vascular-specific genetic modulation on microtubule stability in mouse endothelial cell lines.
analyzed EMT defects in first trimester human abortuses migration assays, immunofluorescence, and qPCR
[AV1]Explain if applying to non-breast cancer jobs
· Studied the role of BCAS3 in vascular development using knock-out mouse, hPSC, breast cancer cell lines, keratinocyte cell lines and endothelial cell lines.[AV1]
· Generated lentiviral mediated genetically modulated hPSCs and characterized their pluripotency and differentiation to all these germ layers by IF, qPCR, and Western Blot.
· Differentiation of hPSCs towards mesenchymal and cardiovascular lineages through 2D, 3D, and spin EB methods.
· Involved in the human iPSC derivation from the primary keratinocytes and smooth muscle cells and their maintenance and creation of cell banks.
· Trained researchers on the culture and maintenance of hPSCs and iPSC lines.