Kristen Maslar
Philadelphia, PA 19147
acz9zz@r.postjobfree.com
EDUCATION:
Drexel University Philadelphia, PA
MS, Cancer Biology July 2017
Thesis: “Investigating the Role of MAPKAP Kinase 2- Mediated RECQ1 Phosphorylation in Triple Negative Breast Cancer”
GPA: 3.86
The University of Scranton Scranton, PA
BS, Biochemistry, Cellular and Molecular Biology May 2015 Honors: Cum Laude
GPA: 3.61
RESEARCH EXPERIENCE:
Drexel University Philadelphia, PA
Graduate Researcher August 2016-Present
Advisor: Todd Strochlic, VMD, PhD August 2015-December 2015
Conducted independent research using phosphoproteomics to validate RECQ1 (RecQ helicase like protein) as a substrate of MK2
Performed a biochemical assay using purified proteins involving techniques such as: western blot, in vitro kinase assay, and mass spectrometry
Validated that RECQ1 is overexpressed in TNBC compared to normal mammary epithelial cells via western blot analysis.
Tested the effects of chemotherapeutic agents on the p38/MK2 signaling pathway by western blot analysis.
Cultured mammalian breast cancer cell lines for experiments involving plasmid transfection and selective drug treatment.
Optimized expression and purification protocol for recombinant RECQ1. Fox Chase Cancer Center Philadelphia, PA
Rotating Graduate Researcher April 2016-June 2016
Advisor: Jeffry Peterson, PhD
Worked collaboratively to treat triple negative breast cancer cells with over 120 metabolic compounds either alone or in combination with doxorubicin or buthionine sulfoximine and measured changes in cell viability via CellTiter Glo Assay. Drexel University Philadelphia, PA
Rotating Graduate Researcher January 2016-April 2016 Advisor: Michael Bouchard, PhD
Conducted independent research that measured change in protein levels to validate increased AKT activation drives cell proliferation in hepatocellular carcinoma due to HBx expression resulting from HBV replication.
MD Anderson Cancer Center Houston, TX
Summer Research Student June 2014 – August 2014
Advisor: Powel H. Brown, MD, PhD
Performed qRT-PCR, immunofluorescence, cell cycle analysis, and cell viability assays to analyze the effect ASPM (abnormal spindle-like microcephaly-associated protein) on triple negative breast cancer proliferation.
The University of Scranton Scranton, PA
Undergraduate Researcher February 2014 – December 2014 Advisor: Tim Foley, PhD
Performed glutathione assay to determine the role of glucocorticoids in neuroblastomas when exposed to different types and concentrations of oxidative stress. KEY LABORATORY SKILLS:
Molecular Biology
o Primer Design,
Sequencing, &
Sequence Analysis
o Molecular Cloning,
Restriction Enzyme
o PCR, qRT-PCR, Site-
directed Mutagenesis
o Western & Southern
Blot
o DNA Extraction,
Purification, & Gel
Electrophoresis
o Cell Transformations
o Mini and Maxi Prep
o Immunofluorescence
Selection and Screening
o Peptide Screen by
Mass Spectrometry
Cell Science
o Bacterial Cell Culture
o Mammalian Cell
Culture
o Mammalian
Transfection
o CellTiter Glo Assay
o Cell Viability Assay
via Trypan Blue
Specialty Software and
Equipment
o Image J
o GraphPad Prism
Assay Development
o In vitro kinase assay
o Dose dependent drug
treatment
Protein Science
o Affinity Purification
OTHER SKILLS:
Excellent written, documentation, and organizational skills
Team-oriented and receptive to suggestions for improvement
Familiar with analyzing data using common biostatistics tests PRESENTATIONS:
Maslar, K, Haricharan, S, Brown P. “The Role of ASPM in Normal, Pre-Malignant, and Invasive Breast Cancer Cells.” CPRIT Undergraduate Research Program, MD Anderson Cancer Center, Houston, TX, August 2014.
REFERENCES AVAILABLE UPON REQUEST