Steinmetz A, Schmidt B, Hocke G, Motzny S, Vitt H, Kaffarnik H
Zentrum Innere Medizin, Endokrinologie und Stoffwechsel, Philipps-Universität, Marburg, Federal Republic of Germany.
Electrophoresis. 1990 Aug;11(8):627-30. doi: 10.1002/elps.1150110808.
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.