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Protein purification systems are intended to isolate one or multiple proteins from a complex mixture. Working with cells, tissues, or whole organisms, the machines purify with predefined start points and editable method templates. With a single click, the compact designed equipment offers real-time run control and visualization. Suitable for even cold-room operations, the products enable you to perform purification of affinity-tagged proteins, antibodies, untagged or native proteins, as well as sample clean-up.
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For intermediate purification and polishing of monoclonal antibodies after the Protein A capture step,giving the possibility to design a two step chromatographic downstream process T
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High binding capacities for column or batch techniques Proven batch-to-batch reproducibility for more than 30 years Very high capacities even at elevated ionic strengths Hydrophilic backbone gives low non-specific binding and high recoveries
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Maximum recovery and minimum nonspecific adsorption with long-term chemical and physical stability resulting from the hydrophilic, rigid allyl dextran/ bisacrylamide matrix.
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Weak cation exchanger based on the well established Sepharose Fast Flow ion exchange platform, extensively used for preparative protein separations in both research and industrial applications.
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Recombinant Protein G type 3 coupled to Sepharose* CL-6B engineered for better binding to rat and mouse IgG subclasses than GammaBind* G at laboratory and process scale
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Glutathione Sepharose High Performance, 25 ml. Excellent for high performance purification of GST-tagged proteinsFast one-step purification of GST-tagged proteins and other glutathione-S-transferase or glutathione-dependent proteins.Glutathione coupled to
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4 Fast Flow is a pre-activated agarose matrix that increases the choice of coupling chemistries available. Suitable for coupling amino-containing smaller proteins and peptides.
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IgG coupled to the highly cross-linked 6% agarose matrix Sepharose* 6 Fast Flow, designed for the rapid purification of protein A and protein A fusion conjugates.Binds at least 2 mg protein A/ml medium.10ml
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The kits are designed for molecular weight determination of proteins with high-resolution gel filtration media and columns such as Superdex*, Superose*, and Sephacryl*.Gel Filtration Calibration Kit LMW and HMW offer:
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Excellent for fractionation of lipids, hormones, vitamins, and other small biomolecules. Designed for use in polar organic solvents and aqueous solvent mixtures.Since Sephadex* LH-20 has such unique properties, we recommend that you consult the publications 25 g
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The kits are designed for molecular weight determination of proteins with high-resolution gel filtration media and columns such as Superdex*, Superose*, and Sephacryl*.Gel Filtration Calibration Kit LMW and HMW offer:
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For removal and/or purification of serine proteases, e.g. thrombin.p-aminobenzamidine (pABA) immobilized on Sepharose* 4 Fast Flow matrix gives high productivity, and allows easy scale-up.High binding capacity..25ml
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Well established, standard aliphatic hydrophobic interaction chromatography (HIC) medium for capture and intermediate purification of larger proteins.
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rProtein A Sepharose* Fast Flow has very high dynamic binding capacity due to its oriented, single-point attachment of protein A.Enhanced binding capacity for immunoglobulins due to the oriented coupling of the ligand.Used in approved MAb processes.25 ml
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Weak anion exchanger, with a different selectivity compared with traditional ion exchangers. It is optimized for the separation of larger proteins
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(high sub) is a weak anion exchanger, with a different selectivity compared with traditional ion exchangers. It is optimized for the separation of larger proteins
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Proteasome purification kit, High integrity kit for purification of proteasome complexes, Isolation of wild type proteasome complexes from biological samples, Analysis of captured proteasome, Comparison of proteasome complexes, Storage: -80 deg C, Size: 10 tests
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Immobilized Concanavalin A is useful for isolating mannose- and glucose-containing glycoproteins.To select the optimum lectin for purification, screen different lectin media, e.g. Con A Sepharose* 4B and Lentil Lectin Sepharose 4B.100 ml
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High binding capacities for column or batch techniques Proven batch-to-batch reproducibility for more than 30 years Very high capacities even at elevated ionic strengths Hydrophilic backbone gives low non-specific binding and high recoveries
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Sephadex* G-25 is the first choice for desalting faster and safer than dialysis.Sephadex* G-25 is ideal for buffer exchange and for removal of free label, e.g..The classic gel filtration medium.500 g
Description:
Sephadex* G-25 is the first choice for desalting faster and safer than dialysis.Sephadex* G-25 is ideal for buffer exchange and for removal of free label, e.g..The classic gel filtration medium.500 g
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