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Single nucleotide polymorphism detection by polymerase chain reaction-restriction fragment length polymorphism.

Abstract：

:Accurate analysis of DNA sequence variation in not only humans and animals but also other organisms has played a significant role in expanding our knowledge about genetic variety and diversity in a number of different biological areas. The search for an understanding of the causes of genetic variants and mutations has resulted in the development of a simple laboratory technique, known as the polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP) method, for the detection of single nucleotide polymorphisms (SNPs). PCR-RFLP allows rapid detection of point mutations after the genomic sequences are amplified by PCR. The mutation is discriminated by digestion with specific restriction endonucleases and is identified by gel electrophoresis after staining with ethidium bromide (EtBr). This convenient and simple method is inexpensive and accurate for SNP genotyping and especially useful in small basic research studies of complex genetic diseases. The whole protocol takes only a day to carry out.

journal_name

Nat Protoc

journal_title

Nature protocols

authors

Ota M,Fukushima H,Kulski JK,Inoko H

doi

10.1038/nprot.2007.407

subject

Has Abstract

pub_date

2007-01-01 00:00:00

pages

2857-64

issue

11

eissn

1754-2189

issn

1750-2799

pii

nprot.2007.407

journal_volume

2

pub_type

杂志文章

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