Gj. Tsongalis et al., IDENTIFICATION OF URINE SPECIMEN DONORS BY THE PM+DQA1 AMPLIFICATION AND TYPING KIT, Journal of forensic sciences, 41(6), 1996, pp. 1031-1034
We evaluated the ability to genotype DNA extracted from urine samples,
which were previously submitted for toxicological analysis, by either
the AmpliType HLA DQ alpha or the combined PM+DQA1 amplification and
typing systems. Initial experiments were conducted on fresh urine, whi
ch was either processed fresh or frozen for one week at -20 degrees C,
from male and female volunteers. Although male urine is noted for con
taining minimal numbers of nucleated cells when compared with female u
rine, we were able to type these samples without difficulty. Male urin
e specimens that were stored frozen for one year in the Toxicology Lab
oratory provided sources of low concentration poor quality genomic DNA
with respect to degradation of nucleic acid. These samples, however,
were also easily typed using the amplification typing kits. Our data,
therefore, suggest that the PM+DQA1 amplification and typing systems d
escribed here are suitable for typing analysis of donor urine specimen
s.