Alberta Paul

Technical Application Specialist at Cytek Biosciences
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Contact Information
us****@****om
(386) 825-5501
Location
Amsterdam, North Holland, Netherlands, NL
Languages
  • Turkish Limited working proficiency
  • English Full professional proficiency
  • Dutch Native or bilingual proficiency
  • German Limited working proficiency

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Credentials

  • Article 9 certified (equivalent to FELASA C)
    -
    Oct, 1995
    - Nov, 2024

Experience

    • United States
    • Biotechnology Research
    • 200 - 300 Employee
    • Technical Application Specialist
      • Jan 2020 - Present

    • United States
    • Higher Education
    • 700 & Above Employee
    • Research Scientist
      • Feb 2017 - Jan 2020

      Rhinovirus human infection study, MHC class II tetramers, spectral flow cytometry, multi dimensional T cell profiles, single cell analysis, allergen specific T cells, CyTOF Rhinovirus human infection study, MHC class II tetramers, spectral flow cytometry, multi dimensional T cell profiles, single cell analysis, allergen specific T cells, CyTOF

    • Türkiye
    • Higher Education
    • 700 & Above Employee
    • Academic Staff
      • Sep 2012 - Jan 2017

       Identification and implementation of diagnostic techniques (identifying genetic defects related to the immune system)  Immunology lecturer medical residents  Council member English Medicine undergraduate program  Social Sciences and Immunology lecturer foreign undergraduates  Coordinator Erasmus Lifelong Learning Programme  Identification and implementation of diagnostic techniques (identifying genetic defects related to the immune system)  Immunology lecturer medical residents  Council member English Medicine undergraduate program  Social Sciences and Immunology lecturer foreign undergraduates  Coordinator Erasmus Lifelong Learning Programme

    • United States
    • Higher Education
    • 700 & Above Employee
    • Research Scientist
      • Jan 2008 - Feb 2010

      Main scientist involved in analysis of the stability of regulatory and effector T cells in the target organ of mice with autoimmune orchitis.  Independently designing and executing experiments  Presentation study result at (inter)national conferences  Organizing journal clubs  Preparation of publications

    • Research Associate
      • Jan 2004 - Jan 2008

      Main scientist involved in analysis of the stability of regulatory and effector T cells in the target organ of mice with autoimmune orchitis.  Independently designing and executing experiments  Presentation study result at (inter)national conferences  Organizing journal clubs

    • Study Director/Postdoc
      • May 2000 - May 2003

      Study director of contract research projects, preclinical evaluation of novel therapeutics in non-human primate autoimmune disease models, for the pharmaceutical/biotechological industry. Responsible for developing, planning and managing several research projects and preclinical studies from start to end including budget management and writing final reports. Postdoc on a one-year pilot project for "The Foundation for the Support of MS Research" aimed at unraveling of the immunopathological… Show more Study director of contract research projects, preclinical evaluation of novel therapeutics in non-human primate autoimmune disease models, for the pharmaceutical/biotechological industry. Responsible for developing, planning and managing several research projects and preclinical studies from start to end including budget management and writing final reports. Postdoc on a one-year pilot project for "The Foundation for the Support of MS Research" aimed at unraveling of the immunopathological events in a novel peptide-induced model of EAE in rhesus monkeys. Identification of CD8 T cell responses against epitopes present in CMV capsid protein and cross-reactive with myelin oligodendrocyte glycoprotein (MOG) and evaluation of their pathogenicity in non-human primates.  Designing, managing and execution of contract research projects (non-human primate autoimmune disease models; RA, IBD, MS)  Time and budget management: Managed over 5 contract research studies with budgets up to $1.000.000  Responsible for ethical approval and monitoring  Writing final reports and progress reports  Communicate with external and internal stakeholders  Recruitment of external and internal stakeholders  Collecting, analyzing, graphical presentation of (clinical) data  Writing publications Postdoc  One-year pilot project for "The Foundation for the Support of MS Research". Immunopathological mechanisms in a new model of EAE in rhesus monkeys  Generation and maintaining of peptide-specific CD8/CD4 T cell lines  Determining cross-reactivity with CMV peptides  Collecting, analyzing, graphical presentation of (clinical) data  Writing publications Show less Study director of contract research projects, preclinical evaluation of novel therapeutics in non-human primate autoimmune disease models, for the pharmaceutical/biotechological industry. Responsible for developing, planning and managing several research projects and preclinical studies from start to end including budget management and writing final reports. Postdoc on a one-year pilot project for "The Foundation for the Support of MS Research" aimed at unraveling of the immunopathological… Show more Study director of contract research projects, preclinical evaluation of novel therapeutics in non-human primate autoimmune disease models, for the pharmaceutical/biotechological industry. Responsible for developing, planning and managing several research projects and preclinical studies from start to end including budget management and writing final reports. Postdoc on a one-year pilot project for "The Foundation for the Support of MS Research" aimed at unraveling of the immunopathological events in a novel peptide-induced model of EAE in rhesus monkeys. Identification of CD8 T cell responses against epitopes present in CMV capsid protein and cross-reactive with myelin oligodendrocyte glycoprotein (MOG) and evaluation of their pathogenicity in non-human primates.  Designing, managing and execution of contract research projects (non-human primate autoimmune disease models; RA, IBD, MS)  Time and budget management: Managed over 5 contract research studies with budgets up to $1.000.000  Responsible for ethical approval and monitoring  Writing final reports and progress reports  Communicate with external and internal stakeholders  Recruitment of external and internal stakeholders  Collecting, analyzing, graphical presentation of (clinical) data  Writing publications Postdoc  One-year pilot project for "The Foundation for the Support of MS Research". Immunopathological mechanisms in a new model of EAE in rhesus monkeys  Generation and maintaining of peptide-specific CD8/CD4 T cell lines  Determining cross-reactivity with CMV peptides  Collecting, analyzing, graphical presentation of (clinical) data  Writing publications Show less

Education

  • PhD Utrecht University
    Doctor of Philosophy (PhD), Immunology
    1995 - 2000
  • Wageningen University
    Master's degree, Biology, General
    1990 - 1994

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