SUSHMA KRISHNAN
***** ***** ****, *** **, Cleveland Heights, Ohio-44106; Ph: 216-***-****; Email: acs8cn@r.postjobfree.com; https://www.linkedin.com/profile/public-profile-settings?trk=prof-edit-edit-public_profile SUMMARY
Enthusiastic biologist with extensive hands on skills in Molecular biology, Genetics, Biochemistry, Immunology, Stem cell biology along with experience in conducting hypothesis driven multidisciplinary research. I am looking forward to translating my academic know-how in an industrial setting. EDUCATION
Case Western Reserve University Cleveland, OH
MSc Biology Jan 2015
Amity University Uttar Pradesh, India
Bachelor of Technology in Biotechnology July 2011
SKILLS
Molecular Biology assays
Protein Chemistry assays
Cell based assays
Viability
Expansion
Proliferation
CFU-F
Erythroid-BFU
MSC phenotyping
T-cell proliferation
Mononuclear cell extraction
Platelet extraction
RBC cryopreservation
Cell lines
Adipose-MSCs Cord blood -MSCs Marrow-HSCs Adult skin fibroblasts Optical Microscopy
Fluorescence
Instruments
BD LSRII
FACS Caliber
Accuri C6
Luminex clinical diagnostic:
Magplex and Bioplex
Automated cell counters:
Emerald Cell Dyn and Heska
UVspectrophotometer
Nanodrop
ELISA Plate reader
Relevant Software skills
FlowJo
FACS Diva
Geneious
DNA star
Sequencher
Softworx image analysis program R
Graphpad Prism
Origin
BLAST
Clustal W
Other skills
SOP writing Knowledge of GMP and GLP Assay Development Human Subject Research PCR
Primer designing
Sanger Sequencing
DNA/RNA extraction
DNA/RNA gels
DNA/Protein Quantification
Plasmid isolation
Competent cell preparation
Transformation
Multi-fragment Cloning
Multiplex assays
SDS PAGE
Western Blot
Protein-Protein conjugation
FACS
Flow cytomtery
ELISA Immunofluorescence Total protein assays
Enzyme assays
WORK EXPERIENCE
NovelMed Therapeutics Cleveland, Ohio
Junior Research Scientist Aug 2015- Present
• Screened hybridoma clones against a pre-selected therapeutic target
• Worked on developing assays for a pharmacodynamic study directed towards a pre-clinical drug product
• Worked on pre-established assays for a pre-clinical drug product
• Interfaced with the various CRO’s the company engages with Compass Biomedical Sciences (part of Arteriocyte) Cleveland, Ohio Research Intern Mar 2015- Aug 2015
• Performed and developed Standard Operating Protocol for culturing cells from punch biopsies in a GMP environment for a client
• Accomplished characterization assay of tissue permeate for a pre-clinical product involved in wound repair (Biobandage™)
• Contributed towards the development of an assay for Human Platelet Lysate (PLUS™ ) to meet requirements for FDA
• Generated scientific data to support (PLUS™ ) as a favorable substitute for animal derived serum
• Posses an operational knowledge and technical know how of Magellan™ autologous platelet separator
• Analyzed and performed flow cytometry on blood samples from compartment syndrome patients Center of Global Health and Diseases, Case Western Reserve University Graduate Research Assistant Aug 2012- Dec 2015
Project 1:
• Established and optimized an Erythrocyte-Binding assay to quantify protein-protein interactions
• Using multiparameter flow cytometry, compared the binding of a recombinant P.vivax erythrocyte invasion protein to chymotrypsin treated and untreated erythrocytes
• Quantified the expression of a transmembrane protein, Duffy antigen, on the erythrocyte surface
• Evaluated the data using FlowJo X and Prism software
• Developed and optimized a protocol for western blot by EDC cross-linking erythrocyte ghosts to vivax invasion protein
• Worked on modifying IRB protocol to integrate volunteer recruitment for this study Project 2:
• Established a Ligase Detection Fluorescent Microsphere assay (LDR FMA) to detect the presence of multiple strain P. vivax infection from vivax-infected Papua New Guinea individuals
• Designed primers around pre-identified SNPs and sanger sequenced the amplified products to detect polyclonal infection
Department of Microbiology and Immunology, Case Western Reserve University
• Assisted in designing an assay to detect the presence of HIV1 in macrophages
• Using fluorescence microscopy and stimulating artificial conditions, we observed the localization of IRF3, transcriptional factor, to the nucleus and cGAS, cytosolic DNA sensor, in the cytoplasm in macrophages National Institute of Malaria Research New Delhi, India Research Assistant Apr - Jul 2011
• Designed primers and PCR amplified short regions of An. culicifacies (sub-species A and B)
• Sanger sequenced and aligned the amplified regions using An. gambiae as the template ABSTRACTS
Krishnan S, Carias L, Grimberg BT, King CL, Zimmerman PA. Plasmodium vivax invasion: Still an enigma? Research showcase poster presentation, Case Western Reserve University, April 2014 Krishnan S, Carias L, Tolia NH, Grimberg BT, King CL, Zimmerman PA. Varying interactions between P. vivax Duffy binding protein and Duffy-positive red cells. American Society for Tropical Medicine and Hygeine, NO, November 2014