An improved method for MN genotyping by the polymerase chain reaction

被引:12
作者
Nakayashiki, N [1 ]
Sasaki, Y [1 ]
机构
[1] IWATE PREFECTURAL POLICE HEADQUARTERS,SCI CRIME DETECT LAB,MORIOKA,IWATE 020,JAPAN
关键词
MN blood group system; genotyping; forensic evidence;
D O I
10.1007/BF01225522
中图分类号
DF [法律]; D9 [法律]; R [医药、卫生];
学科分类号
0301 ; 10 ;
摘要
a novel method of human MN blood group genotyping is reported using the polymerase chain reaction. Genotyping is based on two base substitutions characteristic of M and N alleles in the 2nd exon of the glycophorin A gene. Using a newly designed primer trio, PCR products for M (255 bp) and N (270 bp) alleles are rapidly and simultaneously detected by a single PCR procedure and subsequent polyacrylamide gel electrophoresis. This method enables MN genotyping from not only minute but also degraded DNA samples.
引用
收藏
页码:216 / 217
页数:2
相关论文
共 5 条
[1]   POLYMERASE CHAIN REACTION-BASED DETECTION OF MN BLOOD GROUP-SPECIFIC SEQUENCES IN THE HUMAN GENOME [J].
CORFIELD, VA ;
MOOLMAN, JC ;
MARTELL, R ;
BRINK, PA .
TRANSFUSION, 1993, 33 (02) :119-124
[2]  
HUANG CH, 1991, J BIOL CHEM, V11, P7248
[3]  
NATA M, 1994, DNA POLYMORPHISM, V2, P135
[4]   MOLECULAR-CLONING OF A HUMAN GLYCOPHORIN B CDNA - NUCLEOTIDE-SEQUENCE AND GENOMIC RELATIONSHIP TO GLYCOPHORIN-A [J].
SIEBERT, PD ;
FUKUDA, M .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1987, 84 (19) :6735-6739