1. Quick, easy, convenient.
2. Wide application range. It is suitable for large-scale initial capture or component separation of 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 dynamic loading amount.

Product Datasheet

Matrix	Highly cross-linked agarose and dextran
Particle size range	45-165 µm
Average particle size	90 µm
Binding capacity	180 mg BSA/mL(media)
Ligand	Diethylaminoethyl
Media type	Ion Exchange Medium
Charged group	-N+H2(C2H5)2
Ionic capacity	460-510 µmol Cl-/mL(media)
pH stability	1-14(short term)2-9(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	400-600 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-IE16
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