Suzhou Nanomicro Technology Co., Ltd.
Model No.: UniMab 50L Protein A
Pore Size: 1000
Functional Group: Protein A
Nanomicrotech has the world's leading technology in Chromatography Media, and the company also has rich experiences in the development of purification processes.
Characteristics and Advantages
Highly uniform particles
Uni®Mab affinity chromatography medium has highly uniform particle size distribution and precisely controlled porestructure, as shown in Fig. 1.
Figure 1. SEM diagram of Uni®Mab and a leading brand of protein A medium
High flow rate
Uni®Mab affinity chromatography medium was made from polymethyl methacrylate (PMMA) microspheres (as matrix); and it would withstand the pressure of 0.5 MPa. When compared to an affinity medium with convention alagarose matrix of the chromatography media, it would make the separation process much faster, thus reducing the time purification, for hundreds of liters of large scale chromatography preparative column.(Experimental:Column:4.6 mm × 50 mm Mobile phase:50 mM PBS,0.5 M NaCl)
Figure 2. Comparison of Uni®Mab and a conventional agarose type protein A medium, their pressure vs. linear flow rate.
Excellent loading capacity
At a high flow rate, Uni®Mab showed a significantly better dynamic binding capacity (DBC) than that of the conventional agarose type protein A medium. The same observation was also valid, even when the residence time was increase to 4 - 6 minute.(Experimental:Column:7 mm × 25 mm Sample:Human IgG,2 mg/mL Equilibration buffer:20 mM PBS,pH 7.0 ,0.15 M NaCl Elution:0.1 M Glycine ,pH 3.0)
Figure 3. Comparison of Uni®Mab with a leading brand of Protein A medium, for their dynamic binding capacity
Outstanding pH stability
Uni®Mab affinity chromatography medium could be applied in a pH range from 3 - 12, and it could be cleaned with 0.1 - 0.5 M NaOH. In a life-cycle test, Uni®Mab medium remained greater than 90% of the original dynamic binding capacity (DBC), after 100 CIP cycles with 0.5 M NaOH as CIP reagent. (CIP procedure:Medium:Uni®Mab Column:7 mm × 25 mm Sample:recombinant antibody(chimera) DBC calculation:10% breakthrough Equilibration buffer:20 mM PBS,150 mM NaCl, pH 7.2,3 CV(column volume) Elution:20 mM Citrate,pH 3.0 CIP:0.5 M NaOH,15 CV Re-equilibration:10 CV)
Figure 4. Uni®Mab pH stability in life cycle tests
Uni®Mab was secessfully applied in purification of hIgG from human serum. (Experimental:Column:7 mm× 25 mm Sample:human serum,5 mL Equilibration Buffer:20mM PBS,pH 7.0
0.15 M NaCl Elution:0.1 M Glycine ,pH 3.0 Residence time:4 min )
Figure 5.Uni®Mab used in hIgG purification from human serum
Pre-packed column cartridge
We are proud to be the sole producer (and provider) of monodisperse, super pure silica gel chromatographic media in the world; we also provide monodisperse polymer chromatographic media (these products will match the performance of similar GE products).
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