| Literature DB >> 2289461 |
A Steinmetz1, B Schmidt, G Hocke, S Motzny, H Vitt, H Kaffarnik.
Abstract
On isoelectric focusing of human plasma and subsequent immunoblotting, using antii-human serum amyloid A (SAA) antibodies, a genetic variant of SAA was detected in a family of Turkish origin. All affected members of the family were apparent heterozygotes for the mutant protein, which underwent a charge shift of about one charge unit toward the anode. The variant is likely to be a mutant of the most prominent forms of SAA (SAA1 and SAA2, or SAA1 and SAA1 des Arg). The appearance of a genetic variant of two of the six reported SAA-isoforms in human plasma supports the concept of SAA proteins being products of different genes.Entities:
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Year: 1990 PMID: 2289461 DOI: 10.1002/elps.1150110808
Source DB: PubMed Journal: Electrophoresis ISSN: 0173-0835 Impact factor: 3.535