Affinity – Tosoh Bioscience


Affinity Chromatography (AFC) offers the greatest potential specificity and selectivity for the isolation or purification of biomolecules. Almost all biological molecules can be purified on the basis of a specific interaction between their chemical or biological structure and a suitable affinity ligand.

In AFC, the target molecule is specifically and reversibly adsorbed by a complementary ligand and immobilized on a matrix. Examples of a complementary ligand include an inhibitor, substrate analog or cofactor, or an antibody which specifically recognizes the target molecule. The selectivity is often based on spatial recognition, a ‘lock-and-key’

The adsorbed molecule is subsequently eluted either by competitive displacement or a conformation change through a shift in pH or ionic strength. Typical molecular pairs are antigens and antibodies, enzymes and coenzymes, and sugars with lectins.

Purification of several thousand-fold may be obtained due to the high selectivity of the affinity interactions. Although affinity chromatography is not specific, in that no enzyme interacts with only one substrate, it is the most selective method for separating proteins.

Applications/TSKgel Affinity Columns

The choice of a specific ligand is dictated by the expected interaction between the sample and the bonded phase of the resin used. The TSKgel affinity column line consists of three group specific ligands and one chemically active functionality.

Well known applications for each type of TSKgel affinity column:

Group specific ligands Application
TSKgel Boronate-5PW carbohydrates, nucleic acids, nucleosides, nucleotides, catecholamines
TSKgel Chelate-5PW immunoglobulins, transferrin, lectins, milk proteins, membrane proteins, peptides
Chemically activated ligands Application
TSKgel Tresyl-5PW coupling of ligands to form a custom affinity resin

For more details and prices, please contact MD Scientific via e-mail or phone 7027 8565.