Kit and method of screening wilson's disease
AssigneeZenovac, Inc. (Kr)
InventorsSi Houn Hahn, Young-Ju Jang, Soo-Young Lee, Ha-Cheol Shin, Sun-Young Park, Eun-Sun Yu, Hee-Sung Han
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Abstract
The present invention relates to a method for measuring a ceruloplasmin concentration, and more particularly, to a method for measuring a ceruloplasmin in a blood spot based on a standard concentration curve obtained through an enzyme-linked immunosorbent assay (ELISA) or a dissociation-enhanced time-resolved fluoroimmunoassay using a ceruloplasmin-specific polyclonal antibody or a ceruloplasmin-specific monoclonal antibody.
Claims3
A Wilson's disease screening kit reagent, comprising a ceruloplasmin-specific primary monoclonal antibody;
- a ceruloplasmin-specific secondary monoclonal antibody which recognizes an epitope other than an epitope recognized by the primary monoclonal antibody, wherein the primary and secondary monoclonal antibodies do not neutralize oxidase activity of ceruloplasmin and are an antibody having all of the identifying properties and characteristics of the monoclonal antibody which is secreted from the hybridoma WD-2.1.1 (KCTC 10718BP) or hybridoma WD-1.2 (KCTC 10719BP).
A Wilson's disease screening kit for measuring a ceruloplasmin level in a dried blood spot sample, comprising a ceruloplasmin-specific primary monoclonal antibody;
- and a ceruloplasmin-specific secondary monoclonal antibody which recognizes an epitope other than an epitope that recognized by the primary monoclonal antibody and is conjugated with an enzyme or a lanthanide, wherein said primary and secondary monoclonal antibodies do not neutralize oxidase activity of ceruloplasmin and at least one of said primary and secondary monoclonal antibodies are an antibody having all of the identifying properties and characteristics of the monoclonal antibody which is secreted from the hybridoma WD-2.1.1 (KCTC 10718BP) or hybridoma WD-1.2 (KCTC 10719BP), said blood spot is brought into contact with the primary monoclonal antibody and the secondary monoclonal antibody, and the ceruloplasmin level is determined by comparing the strength of the enzyme of the secondary antibody bound to ceruloplasmin with a standard absorbance curve of ceruloplasmin concentrations.
Dependencies are inferred from the claim text.