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PremiumAKTA avant - User Manual
All users must read the entire Operating Instructions before installing, operating or maintaining the product. Always keep the Operating Instructions at hand when operating the product. Do not install, operate, or perform maintenance on the product in any other way than described in the user documentation. If you do, you may be exposed or expose others to hazards that can lead to personal injury ...
By Cytiva
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Poster: Tips and trips for cannabinoid separation
Object MovedThis document may be found ...
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ReadyCircuit Bags and Tubing Assemblies – Brochure
ReadyCircuit™ assemblies are part of the Cytiva ReadyToProcess™ product platform (Fig 1). ReadyCircuit assemblies allow you to simplify and speed up bioprocessing, thus enabling biopharmaceutical companies, contract manufacturing organizations (CMOs), and biotech start-ups to accelerate product development and reduce costs of initial investments. In addition, single-use ReadyCircuit ...
By Cytiva
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Glutathione S-transferase (GST) Gene Fusion System - Datasheet
The Glutathione S-transferase (GST) Gene Fusion System from Cytiva is a versatile system for the expression, purification, and detection of GST-tagged proteins produced in E. coli. The system consists of three major components: pGEX plasmid expression vectors, products for GST purification, and a variety of GST detection products. A series of site-specific proteases for cleavage of the GST tag ...
By Cytiva
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Sepax C-Pro Cell Processing Instrument - Brochure
The Sepax™ C-Pro Cell Processing System is an automated and functionally closed technology for cell processing when developing and manufacturing cell therapy products. The system, which is comprised of the instrument, Sepax C-Pro protocol software, and kits, allows you to combine multiple processing steps in a versatile manner. These steps include but are not limited to enrichment, magnetic ...
By Cytiva
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SEFIA S-2000 Cell Processing Instrument - Brochure
The Sefia™ multifunctional instrument is designed for cell therapy product manufacturing. The Sefia Cell Processing System, which is comprised of the instrument, protocol software, and disposable kits, allows you to perform upstream or downstream processing steps in a functionally closed and automated manner. You have the flexibility to customize each step to run only the operations you ...
By Cytiva
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AdvanceSTEM Low Osmo Dmem Hyclone Media and Supplements - Brochure
HyClone AdvanceSTEM Low Osmo DMEM is developed to support the growth and maintenance of murine embryonic stem cells (Fig 1). The product’s osmolality has been optimized to approximate murine embryonic ...
By Cytiva
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ADCF-MAb Hyclone Media and Supplements - Brochure
HyClone ADCF-MAb cell culture medium is protein-free and contains no animal-derived components. This regulatoryfriendly medium is developed through the HyClone Metabolic Pathway Design process (see box) to increase the process yields for the manufacture of antibodies and antibody fragments for therapeutic use in a variety of engineered hybridoma and myeloma cell ...
By Cytiva
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ActiPro medium Hyclone Media and Supplements - Brochure
HyClone™ ActiPRO™ cell culture medium has been formulated to provide high yields of recombinant proteins in processes using Chinese hamster ovary (CHO) cell lines (Fig 1). The medium is chemically defined, animal-derived component- free (ADCF), and optimized for high-yield protein production in batch or fedbatch processes. ActiPro medium does not contain any growth factors (such as ...
By Cytiva
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AdvanceSTEM Low Osmo DMEM Hyclone Media and Supplements - Brochure
HyClone™ AdvanceSTEM Low Osmo DMEM is developed to support the growth and maintenance of murine embryonic stem cells (Fig 1). The product’s osmolality has been optimized to approximate murine embryonic tissue. ...
By Cytiva
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COSMETICS LAB Issue 3: Innovation in Formulation
All about spray drying and microencapsulation in the cosmetics industry. ...
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COSMETICS LAB Issue 1: Cosmetics Made with Care
Cosmetics science magazine on product formulation and ...
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Classification, Qualification and Monitoring According to EU GMP Annex 1 Rev 12 - Applications Note
The latest Annex 1 draft has some new definitions and guidance regarding Cleanroom Classification, Qualification, and ...
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USP 797 Revisions and Impact - Application Note
The United States Pharmacopeia (USP) is a scientific non-profit organization that sets standards used worldwide for the identity, quality, purity and strength of medicines, food ingredients and dietary supplements. The organization’s mission is to improve global health through public standards and related programs that help ensure that quality, safety, and benefit of medicines and foods. ...
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Particle Counting in Injectable Solutions - Applications Note
This paper discusses the requirements laid out by US (USP), European (EP), and Japanese (JP) Pharmacopoeia standards and includes the most recent USP <788> (USP 42 2018), EP 5.1 and JP 17 release information. These standards demand that injectable solutions are effectively monitored for microcontamination, specifically nonsoluble ...
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The New EU GMP Annex 1 Revision 2017 Comments from Industry Experts - Applications Note
The updated EU GMP Annex 1 Draft was released for public comment in December 2017, and the industry experts at Particle Measuring Systems have shared their response on the ...
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Xuri Growth Factors Cell Expansion - Datasheet
Growth factors regulate many aspects of cellular function, including proliferation and differentiation. They are widely used for the expansion of T lymphocytes and other primary cell types in cell therapy and research applications. Xuri™ IL-2, IL-15, and IL-21 growth factors are developed following the recommendations of USP <1043> “ancillary materials for cell, gene, and ...
By Cytiva
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DOD - Model PS-7064 - 16-64 Channel Controller - Brochure
The PS-7064 controller provides simultaneous display and alarm functions for up to 64 input variables. 16-32-48-64 channel display modes, and I/O modules arranged in groups of 16 channels, allow economical configuration of systems. This easy-to-configure, user friendly controller is ideal for centralizing display and alarm functions in critical multipoint monitoring ...
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The New EU GMP Annex 1 Draft: Impact on Environmental Monitoring Programs - Application Note
Introduction On December 20th, after intensive research and debates, the draft for a Revision of ANNEX 1 ("Manufacture of Sterile Medicinal Products") of the EU Guideline for GOOD MANUFACTURING PRACTICE for drug products and drug substances was published for public comment. This updated document will set a milestone for adjustments needed within European agencies overseeing drug products ...
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