Rational primer design greatly improves differential display-PCR (DD-PCR).

Abstract:

:Since its conception in 1992, differential display PCR (DD-PCR) has attracted widespread interest. Theoretically an attractive cloning approach, it combines the comparative analysis of several samples with the sensitivity of PCR. Although a large number of studies embracing this technology have been initiated, few novel genes of interest have been identified, suggesting that the method has not realised its potential. The present report shows that by modifying primer design, sampling of differentially expressed genes can be greatly enhanced and relevant genes can be isolated. Using our modified conditions DD-PCR efficiently screens a wide range of gene expression levels, in which differences are represented on a linear scale.

journal_name

Nucleic Acids Res

journal_title

Nucleic acids research

authors

Graf D,Fisher AG,Merkenschlager M

doi

10.1093/nar/25.11.2239

subject

Has Abstract

pub_date

1997-06-01 00:00:00

pages

2239-40

issue

11

eissn

0305-1048

issn

1362-4962

pii

gka362

journal_volume

25

pub_type

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