A new support for affinity chromatography in the form of a gel fibregl
ass (GFG) has recently been invented [Zusman (1992) Isr. Pat. Appl. 10
2948; Zusman (1993) U.S. Pat. Appl. 08/115 087]. The support is prepar
ed from glass fibres covered with oxysilanes so as to provide a 'gel f
ibreglass' matrix. Derivatization of the support eliminates non-specif
ic absorption of proteins. A thin layer of protein trapped in the gel
glass during preparation is created on the surface of a lattice of gla
ss fibres. External agents from the sample for analysis percolate thro
ugh this support and contact a maximum number of molecules of compound
s trapped in the gel glass. The supports are very stable and can be st
ored in dry conditions for a few months at room temperature. The GFG s
uppports were used for affinity chromatography to isolate various prot
eins. A 10-50 mg portion of BSA and human gamma globulin, as well as r
abbit IgG, which were generated against different proteins, were entra
pped in GFG supports, The volumes of the prepared columns varied from
1 to 5 ml. The columns were utilized for isolation of affinity protein
s. The capacity of such supports is up to 12 mg/ml of serum percolated
through a column. The greater the amount of entrapped IgG, the more t
he columns can be re-used. It is shown that the GFG supports have grea
t potential for isolating various macromolecules utilizing specific li
gands.