Insolubilized antibody

Claim 2

An insolubilized antibody for an enzyme immuno assay or radio immuno assay, which has characteristic infrared absorptions at around 1040 cm -1 , 1540 cm -1 and 1640 cm -1 comprising said antibody chemically bonded to cell wall debris of bacteria or yeasts whose shape is globular or rod-like.

Claim 3

The insolubilized antibody according to claim 1, wherein the antibody is chemically bonded to the cell wall debris of bacteria whose shape is globular or rod-like.

Claim 4

The insolubilized antibody according to claim 1, wherein the antibody is chemically bonded to the cell wall debris of yeasts whose shape is globular or rod-like.

Claim 5

The insolubilized antibody according to claim 2, wherein the globular or rod-like bacteria belong to the order Eubacteriales.

Claim 6

The insolubilized antibody according to claim 2, wherein the globular or rod-like bacteria are a member selected from the group consisting of the genus Streptococcus, Staphylococcus, Micrococcus, Lactobacillus, Bacillus, Escherichia and Achromobacter.

Claim 7

The insolubilized antibody according to claim 2, wherein the globular or rod-like bacteria are a member selected from the group consisting of the species of Streptococcus faecalis, Streptococcus salivarius, Streptococcus mutans, Staphylococcus aureus, Micrococcus lysodeiticus, Micrococcus roseus, Lactobacillus plantarum, Bacillus subtilis, Bacillus megatherium, Escherichia coli and Achromobacter aquamarinus.

Claim 8

The insolubilized antibody according to claim 2, wherein the bacteria belong to the species Lactobacillus plantarum.

Claim 9

The insolubilized antibody according to claim 3, wherein the globular or rod-like yeasts are a member selected from the group consisting of the genus Saccharomyces, Pichia and Schizosaccharomyces.

Claim 10

The insolubilized antibody according to claim 3, wherein the globular or rod-like yeasts are a member selected from the group consisting of the species of Saccharomyces cerevisiae, Pichia polymorpha and Schizosaccharomyces pombe.

Claim 11

The insolubilized antibody according to claim 3, wherein the yeasts belong to the species Saccharomyces cerevisiae.

Claim 12

The insolubilized antibody according to claim 1, wherein the antibody is a member selected from the group consisting of the antibodies against the following antigens: hormones, enzymes, virus-specific antigen, tumor antigen, immunogrobulins, human- or bovine-serum albumin and haptens.

Claim 13

The insolubilized antibody according to claim 11, wherein the hormons are a member selected from the group consisting of insulin, tri- or tetra-iodothyronine and human chorionic gonadotropin.

Claim 14

The insolubilized antibody according to claim 11, wherein the haptens are a member selected from the group consisting of diphenylhydantoin, phenobarbital, testosterone and haloperidol.

Claim 15

The insolubilized antibody of claim 1 wherein the antibody is chemically bonded to cell wall debris with a binding agent or by oxidizing the cell wall debris with an oxidizing agent and then reacting the resulting oxidation product with the antibody.

Claim 16

The insolubilized antibody of claim 14 wherein the antibody is chemically bonded to the cell wall debris of bacteria.

Claim 17

The insolubilized antibody of claim 14 wherein the antibody is chemically bonded to the cell wall debris of yeast.

Claim 18

The insolubilized antibody according to claim 14, wherein the binding agent is glutaraldehyde.

Claim 19

The insolubilized antibody according to claim 14, wherein the oxidizing agent is sodium periodate.

Claim 20

The insolubilized antibody according to claim 11, wherein the antibody is a antibody against a hapten which has a partial structure common to that of an antigen to be measured.

Claim 21

A kit for an enzyme immuno assay or radio immuno assay, which comprises the following two components: Component A: an insolubilized antibody which has characteristic infrared absorptions at around 1040 cm -1 , 1540 cm -1 and 1640 cm -1 and comprises an antibody chemically bonded to cell wall debris of bacteria or yeasts whose shape is globular or rod-like, and Component B: an enzyme labeled antigen or a radio isotope labeled antigen.

Claim 22

A kit for an enzyme immuno assay or radio immuno assay, which comprises the following two components: Component A: an insolubilized antibody which has characteristic infrared absorptions at around 1040 cm -1 , 1540 cm -1 and 1640 cm -1 and comprises an antibody chemically bonded to cell wall debris of bacteria or yeasts whose shape is globular or rod-like, and Component B: an enzyme labeled antigen or a radio isotope labeled antigen.

Claim 23

The kit according to claim 20, which is suitable for the assay of any one of the following substances: insulin, human chorionic gonadotropin, immunogrobulins, human serum albumin, tri- or tetra-iodothyronine, diphenylhydantoin, phenobarbital, testosterone and haloperidol.

Claim 24

The kit according to claim 21, which comprises the following components: Component A: an insolubilized antibody comprising an antibody against diphenylhydantoin or a compound having a partial structure common to that of diphenylhydantoin, said antibody being chemically bonded with cell wall debris of Lactobacillus plantarum and Component B: an enzyme labeled antigen comprising β-D-galactosidase bonded to diphenylhydantoin or a compound having partial structure common to that of diphenylhydantoin.

Claim 25

The kit according to claim 21, which comprises the following components: Component A: an insolubilized antibody comprising an antibody against phenobarbital or a compound having partial structure common to that of phenobarbital, said antibody being chemically bonded to cell wall debris of Saccharomyces cerevisiae, and Component B: an enzyme labeled antigen comprising β-D-galactosidase bonded to diazonium salt of m-amino-phenobarbital.

Claim 26

In a method for conducting an enzyme immuno assay or radio immuno assay, which comprises subjecting an enzyme-or radio isotope-labeled antigen, an unlabeled antigen and an antibody to a competitive antigen-antibody reaction in a buffered solution, separating the enzyme- or ratio isotope-labeled antigen bound to the antibody from the free labeled antigen, and determining the amount of the unlabeled antigen by measuring an enzyme activity or radio activity of either the labeled antigen bound to the antibody or the free labeled antigen, the improvement wherein the antibody is an insolubilized antibody which has characteristic infrared absorptions at around 1040 cm -1 , 1540 cm -1 , and 1640 cm -1 and comprises an antibody chemically bonded to cell wall debris of bacteria or yeasts whose shape is globular or rod-like.

Claim 27

In a method for conducting an enzyme immuno assay or radio immuno assay, which comprises subjecting an enzyme-or radio isotope-labeled antigen, an unlabeled antigen and an antibody to a competitive antigen-antibody reaction in a buffered solution, separating the enzyme- or ratio isotope-labeled antigen bound to the antibody from the free labeled antigen, and determining the amount of the unlabeled antigen by measuring an enzyme activity or radio activity of either the labeled antigen bound to the antibody or the free labeled antigen, the improvement wherein the antibody is an insolubilized antibody which has characteristic infrared absorptions at around 1040 cm -1 , 1540 cm -1 , and 1640 cm -1 and comprises an antibody chemically bonded to cell wall debris of bacteria or yeasts whose shape is globular or rod-like.