Abstract
AbstractIn some bloodstains group‐specific component (Gc) forms complexes with blood platelet membrane proteins such as actin which, during isoelectric focusing (IEF), migrate with a lower isoelectric point (pI) than free Gc. When this association occurs it is difficult and sometimes impossible to identify the phenotypes of the Gc system. The problem has been overcome by extracting the bloodstain with 6 M urea prior to IEF. It is then possible to detect and to type Gc in bloodstains that would otherwise not be amenable to Gc typing.
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