Claims Analysis
Total Claims: 5
Claim 1
Independent Claim
82 words
A continuous hybrid cell line which produces and secretes monoclonal antibody specific for soybean Kunitz trypsin inhibitor (KTI) which: (a) re acts and binds with KTI isoforms a and b; (b) does not react with Bowman-Birk inhibitors; (c) does not react with KTI isoforms a and b which have been denatured by moist heat or alkaline treatment or which have been subjected to disulfide exchange; and (d) does not react with KTI isoform c; wherein said cell line is ATCC HB 9517.
Claim 2
Dependent Claim
82 words
A continuous hybrid cell line which produces and secretes monoclonal antibody specific for soybean Kunitz trypsin inhibitor (KTI) which: (a) re acts and binds with KTI isoforms a and b; (b) does not react with Bowman-Birk inhibitors; (c) does not react with KTI isoforms a and b which have been denatured by moist heat or alkaline treatment or which have been subjected to disulfide exchange; and (d) does not react with KTI isoform c; wherein said cell line is ATCC HB 9517.
Claim 3
Dependent Claim
13 words
Monoclonal antibody produced and secreted by the continuous cell line of claim 1.
Claim 4
Independent Claim
572 words
A method for determining KTI isoform composition of a sample, which comprises: (a) mixing a first subsample of a sample with labeled KTI to form a mixture; (b) contacting said mixture with a solid phase coated with monoclonal antibody which binds equivalently to KTI isoforms a, b, and c to obtain solid phase labeled KTI and unbound labeled KTI; (c) separating said solid phase labeled KTI from said unbound labeled KTI; (d) measuring the amount of separated solid phase labeled KTI; (e) determining the amount of KTI in said first subsample by comparing the amount of measured separated solid phase labeled KTI to a standard curve; (f) diluting a second subsample of said sample so that the amount of KTI in said second subsample is within a range of 1 to 3 μg/ml; (g) mixing said diluted second subsample with labeled KTI to form a mixture; (h) taking a first aliquot of said mixture of step (g) and contact said aliquot with a solid phase coated with monoclonal antibody which reacts and binds with KTI isoforms a and b, but does not react with KTI isoform c wherein said monoclonal antibody is produced and secreted by a continuous hybrid cell line designated ATCC HB 9517 to obtain solid phase labeled KTI and unbound labeled KTI; (i) taking a second aliquot of said mixture of step (g) and contacting it with a solid phase coated with monoclonal antibody which reacts and binds with KTI isoforms a and c but does not react with KTI isoform b to obtain solid phase labeled KTI and unbound labeled KTI; (j) separating said solid phase labeled KTI from said unbound labeled KTI in said first and second aliquots; (k) measuring the amount of separated solid phase labeled KTI in said first and second aliquots; (l) preparing a positive control by using a diluent lacking KTI as a control sample and carrying out steps (i)-(k) (m) calculating the percent of separated solid phase labeled KTI bound to each solid phase by comparison to said positive control; (n) distinguishing the isoforms of KTI present in said sample by the following criteria; (i) if the percent of separated solid phase labeled KTI on said solid phase coated with monoclonal antibody which reacts and binds with KTI isoforms a and b but does not react with KTI isoform c is at least 90%, then isoform c is present; (ii) if the percent of separated solid phase labeled KTI on said solid phase coated with monoclonal antibody which reacts and binds with KTI isoforms a and b but does not react with KTI isoform c is less than 75%, then, isoform a, isoform b, or a mixture of a and b is present; (iii) if isoform a, isoform b, or a mixture of a and b is present and the percent of separated solid phase labeled KTI on the solid phase coated with monoclonal antibody which reacts and binds with KTI isoforms a and c but does not react with KTI isoform b is less than 20%, then isoform a is present; and (iv) if isoform a, isoform b, or a mixture of a and b is present and the percent of separated solid phase labeled KTI on the solid phase coated with monoclonal antibody which reacts and binds with KTI isoforms a and c but does not react with KTI isoform b is more than 20%, then isoform b is present.
Claim 5
Independent Claim
572 words
A method for determining KTI isoform composition of a sample, which comprises: (a) mixing a first subsample of a sample with labeled KTI to form a mixture; (b) contacting said mixture with a solid phase coated with monoclonal antibody which binds equivalently to KTI isoforms a, b, and c to obtain solid phase labeled KTI and unbound labeled KTI; (c) separating said solid phase labeled KTI from said unbound labeled KTI; (d) measuring the amount of separated solid phase labeled KTI; (e) determining the amount of KTI in said first subsample by comparing the amount of measured separated solid phase labeled KTI to a standard curve; (f) diluting a second subsample of said sample so that the amount of KTI in said second subsample is within a range of 1 to 3 μg/ml; (g) mixing said diluted second subsample with labeled KTI to form a mixture; (h) taking a first aliquot of said mixture of step (g) and contact said aliquot with a solid phase coated with monoclonal antibody which reacts and binds with KTI isoforms a and b, but does not react with KTI isoform c wherein said monoclonal antibody is produced and secreted by a continuous hybrid cell line designated ATCC HB 9517 to obtain solid phase labeled KTI and unbound labeled KTI; (i) taking a second aliquot of said mixture of step (g) and contacting it with a solid phase coated with monoclonal antibody which reacts and binds with KTI isoforms a and c but does not react with KTI isoform b to obtain solid phase labeled KTI and unbound labeled KTI; (j) separating said solid phase labeled KTI from said unbound labeled KTI in said first and second aliquots; (k) measuring the amount of separated solid phase labeled KTI in said first and second aliquots; (l) preparing a positive control by using a diluent lacking KTI as a control sample and carrying out steps (i)-(k) (m) calculating the percent of separated solid phase labeled KTI bound to each solid phase by comparison to said positive control; (n) distinguishing the isoforms of KTI present in said sample by the following criteria; (i) if the percent of separated solid phase labeled KTI on said solid phase coated with monoclonal antibody which reacts and binds with KTI isoforms a and b but does not react with KTI isoform c is at least 90%, then isoform c is present; (ii) if the percent of separated solid phase labeled KTI on said solid phase coated with monoclonal antibody which reacts and binds with KTI isoforms a and b but does not react with KTI isoform c is less than 75%, then, isoform a, isoform b, or a mixture of a and b is present; (iii) if isoform a, isoform b, or a mixture of a and b is present and the percent of separated solid phase labeled KTI on the solid phase coated with monoclonal antibody which reacts and binds with KTI isoforms a and c but does not react with KTI isoform b is less than 20%, then isoform a is present; and (iv) if isoform a, isoform b, or a mixture of a and b is present and the percent of separated solid phase labeled KTI on the solid phase coated with monoclonal antibody which reacts and binds with KTI isoforms a and c but does not react with KTI isoform b is more than 20%, then isoform b is present.