pall,
颇尔,Heparin HyperD M 肝素亲和层析介质
For the Purification of Biological
Molecules that Bind to Heparin
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Design combines the desirable characteristics of a soft, high speed, high capacity hydrogel with the high dimensional stability of a rigid bead
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Leakage is minimized due to the stable chemical link of the heparin molecule to the sorbent
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Rapid packing due to the high density of the bead
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Can be packed in a variety of column sizes

For the purification of:
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Enzymes (lipoprotein lipase, coagulation enzymes, superoxide dismutase)
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Growth factors (fibroblast growth factor, Schwan cell growth factor)
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Extracellular matrix proteins (fibronectin, vitronectin)
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Nucleic acid binding protein, hormone receptors, and lipoproteins
Average Particle Size
Dynamic Binding Capacity for Human ATIII (10% Breakthrough)1
配基
Immobilized Heparin/mL Sorbent
Working pH
Pressure Resistance
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70 bar (7,000 kPa, 1,000 psi)
Storage Temperature
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.
pall,
颇尔,Heparin HyperD M 肝素亲和层析介质