RESUMO
The polymorphisms of VNTR loci D1S80 (pMCT 118), D17S30 (pYNZ-22 ) and ApoB3' in blood and tissues were detected by amplified fragment length polymorphism (Amp-FLP) technique,and was applied in the paternity testing cases. The discriminating power (DP) of D1S80,D17S30 and ApoB3'were 0. 962, 0. 956 and 0. 960 respectively. The cumulative probability of paternity exclusion (EPP) of the three VNTR loci was 94. 51 %,higher than that of conventional blood typings.
RESUMO
The polymorphisms of minisatellite p33.6 (D1S111) locus were typed rapidly and accurately us- ing polymerase chain reaction (PCR). The amplified fragments were analyzed by mini- polyacrylamide gel electrophoresis followed by silver stain. The distribution of allele frequencies among 100 unrelated Chinese is reported. 14 alleles, containing 9 to 22 repeat units, had been detected with a heterozygosity of 76%. The allele frenquencies were from 0.5 %to 35.5 %. The size of amplified fragments ranged from 435 bp to 925bp. The discrimination power of p33.6 locus was 0. 916. The Amp --FLP was inherited according to the Mendelian Law. The results showed that the polymorphisms of p33.6 locus can be used for individual identification and paternity test.
RESUMO
A region of the D17S30(pYNZ22) locus was amplified in DNA from 120 unrelated chinese individuals was carried out. The amplified products were analysed by mini-polyacrylamide gel electrophoresis followed by silver stain. 11 alleles, ranging from 170bp to 870bp in size and from 0. 4 % to 30. 4 % in frequency, was detected. The heterozygosity was 73%, Dp value was 0.938. The family study showed that the Amp-FLP in pYNZ22 locus is inherited according to the Mendelian law. The correct genotyping results can be obtained from very little amount of biological material, such as mixed stains, blood stains, single hair and saliva.