Procedure for the irreversible binding of proteins onto polystyrene surfaces with retention of their biological activity, polystyrene surfaces obtained by this procedure, and their use

Claim 2

Procedure for the irreversible binding of proteins onto a polystyrene surface, comprising (a) treating a polystyrene surface with a bis-diazonium compound under bis-diazonium compound treating conditions of the general formula I, ##STR4## where R1 stands for a hydrogen atom, a halogen atom, an alkyl group, an alkoxy group or a nitro group and where R2 stands for a hydrogen atom, a halogen atom, an alkyl group and where X stands for an anion and (b) by thereafter adsorbing a protein on to the surface under protein adsorbing conditions.

Claim 3

Procedure according to claim 1, where each R1 is ortho to the nitrogen group and stands for a hydrogen atom, a methyl group or a methoxy group and where each R2 is ortho to the nitrogen group and stands for a hydrogen atom, a methyl group, and where X stands for a halogen or tetrafluoroborate ion.

Claim 4

Procedure according to claim 2, where R1 a stands for a methoxy group, R2 a stands for a hydrogen atom and X stands for Cl - or BF 4 - .

Claim 5

Procedure according to claim 1, where the bis-diazonium compound is in the form of a complex.

Claim 6

Procedure according to claim 1, wherein the protein is an antibody, an antigen, a hapten protein conjugate, an antibody-binding protein, an enzyme or lectin.

Claim 7

A bis-diazonium treated polystyrene vessel or bead suitable for adsorbing proteins prepared by step (a) of claim 1.

Claim 8

A bis-diazonium treated polystyrene vessel or bead having proteins adsorbed thereto prepared according to the procedure of claim 1.

Claim 9

Polystyrene articles according to claim 7, wherein the protein is an antibody, antigen, hapten protein conjugate, antibody-binding protein, enzyme or lectin.

Claim 10

In an immunochemical or enzymatical method for determining the concentration of an analyte in a measured amount of an aqueous sample wherein said aqueous solution is contacted with: (1) an insoluble carrier to which has been attached a biologically active substance capable of reacting with said analyte and (2) a measured amount of a tracer labeled member to form after substantial equilibration a two-phase system containing a solid phase having a portion of the labeled member and unlabeled member bound to said biologically active substance and a liquid phase containing the balance of the unbound labeled member and unlabeled member, (3) the two phases separated and the concentration determined, (4) the improvement comprising using as the insoluble carrier the article prepared by the procedure of claim 1.

Claim 11

A method according to claim 9 wherein the tracer label is selected from the group consisting of a radio label, an enzyme label, a fluorescent label, and a luminescent label.