Experience

Northwestern University

• United States
• Higher Education
• 700 & Above Employee

• Research participant

  • Jan 2016 - Present

  •Studying roles of prion protein in Amyloid Beta oligomers (Abo) induced Alzheimer Disease (AD) related toxic signal platform.•Characterizing roles of prion protein in Abo binding to human neuronal membrane in different AD stages. •Studying roles of prion protein in Amyloid Beta oligomers (Abo) induced Alzheimer Disease (AD) related toxic signal platform.•Characterizing roles of prion protein in Abo binding to human neuronal membrane in different AD stages.



Sun Yat-sen University

• China
• Higher Education
• 400 - 500 Employee

• Undergraduate Research Fellow

  • May 2014 - Sep 2014

  •Cloned the 5α-reductase type I and 3α-hydroxysteroid dehydrogenase (3α-HSD) independently, via experiments including primer designing, plasmid restructuring and electrophoresis.•Injected Neuropeptide Y (NPY) into Tilapia’s Ventricle and detected the expression quantity change of 5α-reductase type I and 3α-HSD with the aid of RT-PCR.•Found out that the THP density of 1ug/g has the best promoting effect on the Tilapia’s food consumption by comparing four groups with different injection densities.



Sun Yat-sen University

• China
• Higher Education
• 400 - 500 Employee

• Research Internship

  • Jan 2012 - Feb 2012

  •Studied on Lipopolysaccharide (LPS)-induced autophagy involved in the restriction of Escherichia coli in peritoneal mesothelial cells. •Utilized different methods to verify the expression of autophagy proteins (LC3) in peritoneal cells, such as western blotting and flow cytometry.•Cultured and identified the peritoneal mesothelial cells by means of Immunofluorescence. •Studied on Lipopolysaccharide (LPS)-induced autophagy involved in the restriction of Escherichia coli in peritoneal mesothelial cells. •Utilized different methods to verify the expression of autophagy proteins (LC3) in peritoneal cells, such as western blotting and flow cytometry.•Cultured and identified the peritoneal mesothelial cells by means of Immunofluorescence.