Literature DB >> 11080693

Application of QuantiGene nucleic acid quantification technology for high throughput screening.

U Warrior1, Y Fan, C A David, J A Wilkins, E M McKeegan, J L Kofron, D J Burns.   

Abstract

To identify inhibitors of interleukin-8 (IL-8) production, a high throughput assay was developed using the QuantiGene nucleic acid quantification kit that employs branched-chain DNA (bDNA) technology to measure the mRNA directly from cells. Unlike polymerase chain reaction and other technologies that employ target amplification, the QuantiGene system uses signal amplification. To perform the assay, various molecular probes capable of hybridizing with IL-8 mRNA were designed and synthesized. A human lung epithelial cell line was treated with interleukin-1alpha (IL-1alpha) to stimulate the IL-8 gene expression and the mRNA was measured using the QuantiGene system. The QuantiGene assay was sensitive, flexible, and reproducible and achieved equivalent or better sensitivity than promoter-reporter assays, and eliminated the time required for constructing a promoter-reporter system. Our data show that bDNA technology has the potential to be used as a high throughput screening assay.

Entities:  

Mesh:

Substances:

Year:  2000        PMID: 11080693     DOI: 10.1177/108705710000500506

Source DB:  PubMed          Journal:  J Biomol Screen        ISSN: 1087-0571


  3 in total

1.  Multiplex mRNA assay using electrophoretic tags for high-throughput gene expression analysis.

Authors:  Huan Tian; Liching Cao; Yuping Tan; Stephen Williams; Lili Chen; Tracy Matray; Ahmed Chenna; Sean Moore; Vincent Hernandez; Vivian Xiao; Mengxiang Tang; Sharat Singh
Journal:  Nucleic Acids Res       Date:  2004-09-08       Impact factor: 16.971

2.  Transcriptional profiling of TLR-4/7/8-stimulated guinea pig splenocytes and whole blood by bDNA assay.

Authors:  Lance K Ching; Farah Mompoint; Jeffrey A Guderian; Alex Picone; Ian M Orme; Rhea N Coler; Steven G Reed; Susan L Baldwin
Journal:  J Immunol Methods       Date:  2011-08-03       Impact factor: 2.303

3.  Glyceraldehyde-3-phosphate dehydrogenase is an inappropriate housekeeping gene for normalising gene expression in sepsis.

Authors:  Michele Cummings; Janahan Sarveswaran; Shervanthi Homer-Vanniasinkam; Dermot Burke; Nicolas M Orsi
Journal:  Inflammation       Date:  2014-10       Impact factor: 4.092

  3 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.