DEAE Chromrose® A50
Matrix: Crosslinked cellulose
Particle size: 40μm~100μm (dry)
Ionic capacity：0.18mmol/mL media
Load capacity/ml: 80mg HSA
Max. flow velocity: 45cm/h
Max. operating pressure: 0.01MPa
pH stability: 2~12
Chemical stability：Stable to commonly used water-soluble buffers and additives, such as 8 M urea and 6 M guanidine hydrochloride.
Storage: 2℃~30℃
Particle size: 40μm~100μm (dry)
Ionic capacity：0.18mmol/mL media
Load capacity/ml: 80mg HSA
Max. flow velocity: 45cm/h
Max. operating pressure: 0.01MPa
pH stability: 2~12
Chemical stability：Stable to commonly used water-soluble buffers and additives, such as 8 M urea and 6 M guanidine hydrochloride.
Storage: 2℃~30℃
Ion exchange chromatography is one of the most widely used methods for the separation and purification of proteins and is a process that separates different biomolecules based on differences in their surface charges (type, amount and distribution). DEAE Chromrose® A50 is based on dextran gel G50 with DEAE as ligand and is suitable for the separation and purification of biomolecules of medium-sized molecules, which are often used for the separation of prothrombin complexes in blood products.
Application scenarios:
Commonly used in blood products for prothrombin Prothrombin complexes in blood products.
