A homogeneous method to quantify mRNA levels: a hybridization of RNase protection and scintillation proximity assay technologies.

Abstract:

:A novel method to measure mRNA levels has been developed by combining the detection capabilities of RNase protection (RPA) with the quantification advantages of scintillation proximity assay (SPA) technology. Sample processing is reduced to the addition of a single reagent post RNase digestion. As a model system, the inducible expression of rat apolipoprotein-A1 mRNA has been measured by both traditional gel-based RPAs and the SPA-based RPA assay. Results demonstrate that the ribonuclease protection proximity assay (RiPPA) faithfully reproduces the gel-based results and is at least as sensitive as many existing methods.

journal_name

Nucleic Acids Res

journal_title

Nucleic acids research

authors

Kenrick MK,Jiang L,Potts CL,Owen PJ,Shuey DJ,Econome JG,Anson JG,Quinet EM

doi

10.1093/nar/25.14.2947

subject

Has Abstract

pub_date

1997-07-15 00:00:00

pages

2947-8

issue

14

eissn

0305-1048

issn

1362-4962

pii

gka441

journal_volume

25

pub_type

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