Lei Xu, MS.
Cupertino, CA 95014
C: 650-***-****
E-mail: ****@*******.***
Objectives:
To join a dynamic team in development and implementation of novel
technologies in biomedical sciences.
Technical Skills:
1.Working experience at Amgen as a research associate
2. Two year Drug discovery research experience.
In Cell Western: Phospho ACC on HepG2 and H1299 cell lines; Membrane
immobilized ligand binding assay (plate assay) of adiponectin; Cell
membrane preparation; western blot analysis. PRK plate assay;
3. Proficient in major molecular biology techniques including:
Antibody Expression. DNA isolation and purification. RNA isolation and
purification. Protein isolation. Southern dot blot. Northern blot. Western
blot analysis. Molecular cloning. UV/VIS spectrophotometry. In vitro
transcription. Immunofluorescence staining. DNA sequencing. DNA fragment
sequencing with genome walker kit. RNase protection assays. Restriction
enzyme analysis. Immunopanning. PCR. RT-PCR. TaqMan. Primer and probe
designing. ELISA. Sequencher analysis. Up-Scaling Protein expression with
Roller Bottles.
4.. Extensive experience in major cell biology techniques including:
Established and maintained stable cell lines and human primary cell lines
Primary and secondary tissue Culture (Cell culture). In vitro cell-based
assays. Mammalian cell transfection (electroporation and lipofection).
5. In vivo animal models including:
Small animal handing and Stereotaxic Intracerebral Injection. Analyzing
DNA and RNA from animal tissues.
6. Proficient in searching biochemical information from internet and using
computer programs including Word, PowerPoint, Adobe Photoshop, and Exel.
7. A self motivated, hardworking, and team player. Good communication and
problem solving skills and data analysis. Effective multi-tasking skills,
strong organizational, and record keeping.
Research Experience:
1. 01/2009-04/2010
Research consultant
Worked on drug development project.
2. 4/2007-10/2007
Research associate
Amgen Inc.
Participated in Antibody engineering project (Adiponectin protein
engineering); Involved in cloning service. Transfection; Up-Scaling Protein
expression with Roller Bottles. Western blot.
3. 2/2005-2/2007
Research Associate
Rigel Pharmaceuticals, Inc.
Participated in Drug discovery Project (Diabetes disease type 2 with
Adiponectin)
Developed cell based assays (In Cell Western: Phospho ACC on HepG2 and
H1299 cell lines) Enzyme kinetics (PRK plate assay), Assay development and
automated liquid handling; Membrane immobilized ligand binding assay (plate
assay) of adiponectin; Cell membrane preparation; western blot analysis.
PRK plate assay. Experience with cell based assay readouts of receptor
ligand interactions.
4. 5/2004-10/2004
Research Associate (Temp)
Cell Genesys Inc.
Worked on Anti-Angiogenesis projects.
Constructed many antibody expression vectors.
Cell based assays. Cultured CHO cell line, 293 cell line and NSO cell line.
Transient transfection. Antibody Expression. ELISA.
5. 6/2001-4/2003
Research Associate
Sangamo Biosciences, Inc.
Participated in the gene therapy projects in the cardiovascular therapeutic
team (Angiogenesis).
Analyzed many gene expression levels such as mouse, rat and human VEGF mRNA
with real time quantitative RT-PCR (Taqman).
Designed many Taqman primer and probe sets including various VEGF isoforms.
Performed ELISA and Western blot analysis to quantitate and detect VEGF
protein expression.
Cultured many different types of cells including primary cell culture and
induced differentiated skeletal muscle cells. Lipo-transfected SKMC and 293
cells with plasmid DNA (in vitro cell-based assays).
Made and validated the VEGF in situ DIG-labeled RNA probes to detect VEGF
expression level in mouse tissues with In vitro transcription kit.
Sequenced many DNA fragments, such as pig FGF5, Pig VEGF and Rabbit VEGF
promoter regions using the Genome Walker kit.
6. 7/1999-6/2001
Researcher
Dept. of Neurosurgery, Stanford University
Worked on the gene therapy project for brain tumors (Oncology).
Worked on neuronal transplantation project for Parkinson's disease.
Used semi-quantitative RT-PCR to quantitate the expression level of
angiopoietin factors such as ang-1, ang-2, VEGF, and Tie-2 in the glioma
rat model.
Verified that sonic hedgehog promotes early postnatal sympathetic cell
proliferation and promotes tyrosine hydroxylate induction of sympathetic
cells in vitro using immunofluorescence staining
7. 1/1996-5/1999
Master of Science and Research Assistant
Dept. of Biology, University of South Alabama
Gained considerable expertise in cellular and molecular biology approaches.
Constructed an antisense Beta globin cDNA gene expression vector.
Established and maintained stable cell lines and human primary cell lines.
Transfected antisense Beta globin cDNA expression vector into mouse
erythroleukemia cells and human primary erythroid progenitors by
electroporation.
Analyzed RNA expression level by RNA protection assay.
Education:
1. 1/1996-5/1999
Dept. of Biology, University of South Alabama
Master of Science
2. 9/1981-6/1987
Shanghai Medical University, Shanghai, P.R.China
Doctor of Medicine
Publications and Abstracts:
Rebar EJ, Huang Y, Hickey R, Nath AK, Meoli D, Nath S, Chen B, Xu L, Liang
Y, Jamieson AC, Zhang L, Spratt SK, Case CC, Wolffe A, Giordano FJ.
Induction of angiogenesis in a mouse model using engineered transcription
factors. Nature Medicine. 2002. 8(12): 1427-32.
Williams, Z., Tse, V., Hou, L., Xu, L., and Silverberg, G., Sonic hedgehog
promotes proliferation and tyrosine hydroxylase induction of postnatal
sympathetic cells in vitro. NeuroReport. 2000. 11(15):3315-3319.
Xu, L., A.E.Terry, C. Monteiro, and B.S.Pace. Enhanced Gamma globin
biosynthesis by antisense beta globin RNA transcripts. Gene Therapy. 2000.
7:438-444.
Xu, L., and B.S.Pace. 1998. Modulated human globin gene expression: Role of
antisense expression vectors. Cell.Mol.bio.Letters. 1998. 3:423-433.
Edward JR., L. Zhang, Y. Lee, Y. Liang, L. Hinh, B. Johnstone, L. Xu, CL.
Dent, P. Liu, X. Li, TD. Schaal, EJ. Wolffe, SK. Spratt, J. Rokovich**, CC.
Case, CO. Pabo. Robust Activation of Vascular Endothelial Growth Factor-A
Using Designed Zinc Finger Protein Transcription Factors. The 6th American
society of gene therapy, May, 2003, Washington, DC.
Xu, L., C. Monteiro, and B.S.Pace. Suppression of human Beta globin chain
synthesis mediated by a mammalian antisense expression vector. Presented at
the American society of gene therapy, May, 1998, Seattle, WA.