Kit for detecting human chorionic gonadotropin

Claim 1

A diagnostic test kit for detecting the absence or the presence of suspected malignant neoplastic cells in a cell specimen by testing for human chorionic gonadotropin, said diagnostic cell test kit comprising: (a) antiserum specific to the beta-subunit of human chorionic gonadotropin, said beta-subunit having been raised in a host animal, for treating cell samples to be tested, followed by rinsing to remove any excess antiserum; (b) antiserum specific to gamma globulin of said host animal conjugated to fluorescein for adding to a portion of said sample to be tested which has been treated with said beta-subunit of human chorionic gonadotropin followed by examination of said portion with an ultraviolet microscope which passes the ultraviolet light through said cells; if fluorescein is found, the indirect fluorescein-labelled antibody test is considered positive; if no staining is found, this indirect test is considered negative; and (c) antiserum specific to said gamma globulin of said host animal conjugated to peroxidase for adding to a second portion of said cell specimen treated with said antiserum specific to the beta-subunit of human chorionic gonadotropin and peroxidase activator, added to said second cell sample followed by an examination of said second portion with a microscope to determine whether peroxidase staining has occurred, the indirect peroxidase-labelled antibody test is considered positive if staining is found; if no staining is found, the test is negative; the cell test for human chorionic gonadotropin is then considered positive only if both indirect labelled antibody tests are positive; if both indirect antibody tests are negative or if one indirect labelled antibody test is positive and the other is negative, the diagnostic cell test is negative for human chorionic gonadotropin, establishing that neoplastic cells are not present in the cells tested.