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36 Results Found

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  1. Inactivation and removal of Zika virus during manufacture of plasma‐derived medicinal products

    Author
    Blumel, J. et al
    Organization
    Paul-Ehrlich-Institut
    Publisher
    Transfusion 2017 (57) 790-796
    Year
    2017
    Access
    Open
  2. cGMP production and analysis of BG505 SOSIP.664, an extensively glycosylated, trimeric HIV‐1 envelope glycoprotein vaccine candidate

    Author
    Dey, A., et al
    Organization
    International AIDS Vaccine Initiative, Department of Microbiology and Immunology, et al
    Publisher
    Biotechnology and Bioengineering 2018 (115) 885–899
    Year
    2018
    Access
    Open
  3. Hepatitis E virus derived from different sources exhibits different behaviour in virus inactivation and/or removal studies with plasma derivatives

    Author
    Yunoki, M., et al
    Organization
    Japan Blood Products Organization
    Publisher
    Biologicals 44(5) 403-411
    Year
    2016
    Access
    Abstract Only
  4. Pathogen safety of a pasteurized four‐factor human prothrombin complex concentrate preparation using serial 20N virus filtration

    Author
    Nowak, T., et al
    Organization
    CSL Behring
    Publisher
    Transfusion 57(5) 1184-1191
    Year
    2017
    Access
    Open
  5. Pathogen Safety of a New Intravenous Immune Globulin 10% Liquid

    Author
    Radomski, K., et al
    Organization
    Octapharma Biopharmaceuticals GmbH
    Publisher
    BioDrugs (2017) 31: 125
    Year
    2017
    Access
    Open
  6. Evaluation of the virus clearance capacity and robustness of the manufacturing process for the recombinant factor VIII protein, turoctocog alfa

    Author
    Ellgaard, T., et al
    Organization
    Novo Nordisk A/S
    Publisher
    Protein Expression and Purification 129 (2017) 94-100
    Year
    2017
    Access
    Open
  7. Validation of the manufacturing process used to produce long-acting recombinant factor IX Fc fusion protein

    Author
    McCue, J., et al
    Organization
    Biogen
    Publisher
    Haemophilia 20(4): e327-e335
    Year
    2014
    Access
    Open
  8. BAY 81-8973, a full-length recombinant factor VIII: manufacturing processes and product characteristics

    Author
    Garger, S., et al
    Organization
    Bayer
    Publisher
    Haemophilia 23(2): e67-e78
    Year
    2017
    Access
    Open
  9. Manufacturing process used to produce long-acting recombinant factor VIII Fc fusion protein

    Author
    McCue, J., et al
    Organization
    Biogen
    Publisher
    Biologicals 43: 213–219
    Year
    2015
    Access
    Open
  10. Pathogen safety and characterisation of a highly purified human alpha1-proteinase inhibitor preparation

    Author
    Kee, S., et al
    Organization
    CSL Behring
    Publisher
    Biologicals 47: 25–32
    Year
    2017
    Access
    Open