Appeal No. 93-3369 Application 07/344,179 unbound in order for sample DNA (G) to hybridize to it. See Figure 1B of Diamond. The DNA hybridization assay would not operate if all of the target region of the probe (TBR) was “saturated” by being bound to labeled polynucleotide (L). Similarly, the device taught by Liotta could not operate if substantially all of the antibody binding sites are saturated prior to addition of the sample. The device of Liotta requires the binding sites to be freely available. Saturation will occur either with the binding partner in the sample or the binding partner in the immobilized phase if the sample is free of the binding partner. See column 3, lines 17-25 in conjunction with Figures 5 and 6 of Liotta. As depicted in those figures the antibody is labeled. If there is antigen in the sample it will occupy the binding sites of the labeled antibody. By so occupying the binding sites the antibody will not become trapped by binding to the immobilized antigen in Zone 1, thus it will pass on to Zone 2 and the presence of the label will be detected by a visible color reaction in Zone 2. When the sample is free of antigen the labeled antibody will move into the region containing the immobilized antigen where it will be trapped via binding to 15Page: Previous 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 NextLast modified: November 3, 2007