1. Quick, easy, convenient.
2. Wide application range. It is suitable for component separation or fine purification of all types of charged biomolecules.
3. The purification process is highly flexible, and the purity of the sample can be improved by screening the purification conditions in earlier stage.
4. High binding capacity (compared with other types of chromatographic media).

Product Datasheet

Matrix	Highly cross-linked 6% agarose
Particle size range	45-165 µm
Average particle size	90 µm
Binding capacity	90 mg BSA/mL(media)
Ligand	Quaternary amine
Media type	Ion Exchange Medium
Charged group	-N+(CH3)3
Ionic capacity	180-360 µmol Cl-/mL(media)
pH stability	1-14(short term)2-12(working)2-12(long term)
Chemical stability	All of the commonly used buffers, 1M NaOH, 70% Ethanol, 8M urea, 6M Guanidine hydrochloride. Avoid of oxidizing agent, anionic detergent and anionic buffer
Maximum flow rate	200-300 cm/h (0.3MPa, XK16/40. Column bed height:30 cm)
Pressure	≤0.3 MPa
Storage buffer	20% Ethanol
Storage temperature	4~30℃

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Cat. No	E-CM-IE09
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