Invader Assay for RNA Quantitation
By: Marilyn C. Olson2, Tsetska Takova2, LuAnne Chehak2, Michelle L. Curtis2, Sarah M. Olson2, Robert W. Kwiatkowski2
| Abstract |
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The Invader® assay is a homogeneous, isothermal, signal amplification system for the quantitative detection of nucleic acids.
The assay can directly detect either DNA or RNA without target amplification or reverse transcription. It is based on the
ability of Cleavase® enzymes to recognize as a substrate and cleave a specific nucleic acid structure generated through the
hybridization of two oligonucleotides to the target sequence. The combination of sequence-specific oligo-nucleotide hybridization
and structure-specific enzymatic cleavage results in a highly specific assay well suited for discriminating closely related
gene sequences. This includes detection of single nucleotide polymorphisms directly from genomic DNA as well as highly homologous
mRNAs in closely related gene families. Because Cleavase® substrate recognition is structure, and not sequence dependent,
cleavage and detection can be applied to virtually any DNA or RNA sequence.
Book Title: Gene Expression Profiling: Methods and Protocols
Series: Methods in Molecular Biology | Volume: 258 | Pub. Date: Feb-24-2004 | Page Range: 53-69 | DOI: 10.1385/1-59259-751-3:53
Subject: Genetics/Genomics
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