Heparin HyperD® M Affinity Chromatography Sorbent
For the Purification of Biological
Molecules that Bind to Heparin
- Design combines the desirable characteristics of a soft, high speed, high capacity hydrogel with the high dimensional stability of a rigid bead
- Leakage is minimized due to the stable chemical link of the heparin molecule to the sorbent
- Rapid packing due to the high density of the bead
- Can be packed in a variety of column sizes
For the purification of:
- Enzymes (lipoprotein lipase, coagulation enzymes, superoxide dismutase)
- Growth factors (fibroblast growth factor, Schwan cell growth factor)
- Extracellular matrix proteins (fibronectin, vitronectin)
- Nucleic acid binding protein, hormone receptors, and lipoproteins
Particle Size
- 80 µm (average)
Dynamic Binding Capacity for Human ATIII (10% Breakthrough)1
- 25 mg/mL
Ligand
- Porcine Heparin
Immobilized Heparin/mL Sorbent
- 5 - 10 mg/mL
Working pH
- 3 - 13
Pressure Resistance
- 70 bar (7,000 kPa, 1,000 psi)
Storage Temperature
- 2 - 8 ° C (36 - 46 ° F)
1Determined using human ATIII at 72.5 UI/mL in 20 mM TrisHCl, 0.3 M NaCl, pH 7.4. Elution with 20 mM Tris HCl, 2 M NaCl, pH 7.4 at a flow rate of 600 cm/h, 10 cm (4 in.) bed height.
Dynamic Binding Capacity vs. Linear Velocity

Column dimensions: 0.46 cm I.D. x 10 cm; Sample: HU ATIII at 72.5 μL/mL; Equilibration buffer: 20 mM Tris-HCl containing 0.3 M NaCl, pH 7.4.
Pressure vs. Linear Flow Velocity
Column dimensions: 0.46 cm I.D. x 10 cm; Buffer: 20 mM Tris-HCl containing 0.3 M NaCl, pH 7.4.
Contact Customer Service at 800-521-1520 for possible lead-time and ship date.
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