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filingDate 1988-06-20-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_b154db58a6486d0a7295371429c1eb66
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publicationDate 1988-12-21-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber EP-0295719-A2
titleOfInvention The SM-D antigen, the cloning of the SM-D antigen and the detection of systemic lupus erythematosus by using the SM-D antigen
abstract snRNP proteins are isolated, as by immunoaffinity chromatography, using antibodies from a serum sample of a living being affected by systemic lupus erythematosus. The Sm-D polypeptide is in turn isolated from the snRNP protein complex as by gel electrophoresis and electroelution. The amino terminus of the Sm-D polypeptide is then sequenced, and labelled DNA probes with nucleotide sequences complementary to that encoding the amino acid sequence are synthesized. A human cDNA library in a lambda cloning vector is transferred to appropriate filters such as nitrocellulose filters. These filters are screened as by hybridization with the labelled probes to identify the cDNA clones in the library with sequences matching those of the labelled probes. The cDNA encoding the Sm-D protein is then subcloned. The Sm-D polypeptide is then isolated as by immunoaffinity chromatography and, if further desired, as by HPLC chromatography. An assay is then made with the isolated Sm-D polypeptide by reacting the Sm-D polypeptide with a serum sample of a living being to determine whether the living being is affected by systemic lupus erythematosus. The assay may be performed as by an enzyme-linked immunoabsorbant such as anti-human IgG/IgM antibodies covalently attached to an enzyme indicator. Lactoperoxidase/alkaline phosphatase are each an example of an enzyme indicator to indicate, as by distinctive color, an affected person.
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