products, brochures and datasheets

71. Perfusion & Concentrated Perfusion Technology 6/29/2011
    Recirculating hollow fiber systems have been used for a long time with mixed results. The recurring problem with these and all other cell retention systems is the difficulty in scaling up and staying sterile.
72. Macro-Prep® High S Support 4/1/2008
    Macro-Prep ion exchange media meet the demands of analytical, semipreparative, and process-scale applications. These rigid macroporous, hydrophilic 50 µm media provide exceptional capacity, resolution, and throughput in a chemically and mechanically stable form. Macro-Prep media operate well at low and medium pressures and exhibit minimal volume changes in response to variations in pH or ionic strength
73. Cholera Toxin A (CTA) or B (CTB)subunits 12/8/2000
    CTA subunit bears the ADP-ribosyl-transferase activity of the toxin which deregulates the Gs protein causing activation of adenylate cyclase
74. Recommended Cleaners For Biopharma 6/27/2013

    From spinner flasks to production fermentation tanks, Alconox detergents can eliminate cross-contamination and assure reliably clean equipment for all of your biotechnology cleaning needs. Even difficult accumulated biomaterial residues on fermentation vessel agitation shafts, thermowells, harvest tubes, sparger tubes, and the bevel tips of addition ports easily come clean with Alconox detergents.

75. Sterility Testing: An Essential Part Of Pharmaceutical Product Validation

    To effectively monitor product quality, it is critical to test for microbial contamination throughout the pharmaceutical manufacturing process. Sterility testing is a vital step to ensure products purporting to be sterile do not contain viable microorganisms prior to their distribution and administration to patients. Consequently, it is of utmost importance that the testing method employed for products, formulations, tissue materials, and medical devices is both accurate and reliable. Explore a collection of streamlined sterility testing solutions and expert guidance on sterility testing, quality control (QC), and data integrity. Optimize your sterility testing and QC procedures with world-leading tools and technologies that can help you ensure full traceability and regulatory compliance.

76. Downstream Processing 11/8/2007
    At Laureate, we use automated chromatography development systems to scale up from bench to manufacturing, develop robust well-integrated processes and produce high purity product with good yield. From sample preparation to initial capture to polishing and final product formulation, our experienced team can purify any protein product to full cGMP requirements.
77. Modern MES Software For Drug Manufacturing 9/19/2024

    Eliminate errors and accelerate production with MasterControl MES.

    MasterControl Manufacturing Excellence is a modern manufacturing execution system (MES) that has helped hundreds of manufacturers eliminate millions of errors and deliver products to the market 70% faster.

    It’s time to modernize your manufacturing operations – from digital work instructions and production records (EBR/eDHR) to electronic logbooks and equipment tracking – and see how MasterControl Manufacturing Excellence software can help you run faster, leaner, and smarter.

78. Potent Antibiotic for Selection 2/10/1999
    Bleocin is a DNA-cleaving glycopeptide that exerts its toxic effect on
79. BINDER FED Series - Heating Chambers With Forced Convection 6/25/2008
    The FED series is a true all-rounder. It has a virtually unlimited capacity and is at the same time particularly adaptable to the specific requirements of a large variety of testing applications. The enhanced time functions and the digitally controlled air turbine can be used to adjust ideal temperature parameters and recirculation air conditions
80. Continuous Effluent Decontamination (CED) System 12/17/2009
    Designed to replace kill tanks, the innovative CED System is the newest hazardous fluid decontamination technology in decades. The system provides safe, validatable, continuous effluent flow decontamination for BL-3 and BL-4 labs, biological containment facilities, and animal production and comparative medicine facilities.