Abstract
Reliable and sensitive single target copy detection, as well as selection of reliable reference genes for precise gene expression analysis, are still challenges for real-time PCR users. We introduce a system that enables robust and highly sensitive probe-based real-time PCR, provides a novel, antibody-mediated, hot-start mechanism for highly specific target detection, and allows flexible combinations of high and low abundant target and reference genes for accurate gene expression results.
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Taswell C (1987) Limiting Dilution Assays for the Separation, Characterization and Quantitation of Biologically Active Particles and Their Clonal Progeny. In: Pretlow TG, Pretlow TB (Hrsg) Cell separation: Methods and selected applications, Band 4. Academic Press, Waltham, MA, 109–145
Karge WH 3rd, Schaefer EJ, Ordovas JM (1998) Quantification of mRNA by polymerase chain reaction (PCR) using an internal standard and a nonradioactive detection method. Methods Mol Biol 110:43–61
Thellin O, Zorzi W, Lakaye B et al. (1999) Housekeeping genes as internal standards: use and limits. J Biotechnol 75:291–295
Dheda K, Huggett JF, Bustin SA et al. (2004) Validation of housekeeping genes for normalizing RNA expression in realtime PCR. Biotechniques 37:112–114
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Irle, I., Traeger, T. & Missel, A. Akkurate Detektion seltener Gene und flexible Auswahl der Referenzgene. Biospektrum 19, 766–767 (2013). https://doi.org/10.1007/s12268-013-0390-1
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DOI: https://doi.org/10.1007/s12268-013-0390-1