Abstract
The Polymerase Chain Reaction (PCR) can enhance the detection of known VNTR loci, particularly in forensic situations where limited amounts of DNA are available. PCR amplification of several polymorphic VNTR regions has been described. Here, we describe the application of the DNA-amplification technique for the detection of three variable minisatellite loci: the VNTR loci D1S80 (D1S58) and D17S30 (D17S5) and the hypervariable region 3′ of the apolipoprotein B gene. Polymorphic PCR-fragmenta were detected on ethidiumbromide stained polyacrylamide gels.
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Literature
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© 1992 Springer-Verlag Berlin Heidelberg
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Kloosterman, A., Vossen, R., Wust, D., de Leeuw, W., Uitterlinden, A. (1992). Detection of Three Different VNTR’s by DNA-Amplification. In: Rittner, C., Schneider, P.M. (eds) Advances in Forensic Haemogenetics. Advances in Forensic Haemogenetics, vol 4. Springer, Berlin, Heidelberg. https://doi.org/10.1007/978-3-642-77324-2_13
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DOI: https://doi.org/10.1007/978-3-642-77324-2_13
Publisher Name: Springer, Berlin, Heidelberg
Print ISBN: 978-3-540-55194-2
Online ISBN: 978-3-642-77324-2
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