Abstract
The LightCycler** system performs real-time PCR with specific and quantitative analysis of amplified products. All parameters of the PCR reaction have to be carefully adjusted. The most important factors are DNA quality and concentration. Pure DNA is prepared with any manufactured kit. Quantification of genomic DNA samples is essential for accurate quantification of small differences in gene copy numbers or low copy target genes. Classic methods used to quantify genomic DNA have limitations.
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© 2002 Springer-Verlag Berlin Heidelberg
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Pieri-Balandraud, N., Roudier, J., Roudier, C. (2002). Quantification of Human Genomic DNA Using Retinoic X Receptor B Gene. In: Dietmaier, W., Wittwer, C., Sivasubramanian, N. (eds) Rapid Cycle Real-Time PCR — Methods and Applications. Springer, Berlin, Heidelberg. https://doi.org/10.1007/978-3-642-59397-0_4
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DOI: https://doi.org/10.1007/978-3-642-59397-0_4
Publisher Name: Springer, Berlin, Heidelberg
Print ISBN: 978-3-642-63965-4
Online ISBN: 978-3-642-59397-0
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