SwePub
Sök i LIBRIS databas

  Utökad sökning

WFRF:(Hedman Johannes)
 

Sökning: WFRF:(Hedman Johannes) > Digital PCR inhibit...

Digital PCR inhibition mechanisms using standardized inhibitors representing soil and blood matrices

Sidstedt, Maja (författare)
Applied Microbiology, Department of Chemistry at Lund University; Swedish National Forensic Centre (NFC)
Romsos, Erica L. (författare)
National Institute of Standards and Technology (NIST)
Hedell, Ronny (författare)
wedish National Forensic Centre (NFC)
visa fler...
Ansell, Ricky (författare)
Linköpings universitet,Biologi,Tekniska fakulteten,Swedish National Forensic Centre, Linköping, Sweden
Steffen, Carolyn R. (författare)
National Institute of Standards and Technology (NIST)
Vallone, Peter M. (författare)
National Institute of Standards and Technology (NIST)
Rådström, Peter (författare)
Applied Microbiology, Department of Chemistry at Lund University, Sweden
Hedman, Johannes (författare)
Applied Microbiology, Department of Chemistry at Lund University, Sweden; National Institute of Standards and Technology (NIST)
visa färre...
 (creator_code:org_t)
2016
2016
Engelska.
  • Konferensbidrag (övrigt vetenskapligt/konstnärligt)
Abstract Ämnesord
Stäng  
  • Digital PCR (dPCR) enables absolute quantification of nucleic acids by partitioning the sample into hundreds or thousands of minute reactions. By assuming a Poisson distribution for the number of DNA fragments present in each chamber, the DNA concentrationis determined without the need for a standard curve. However, when analyzing nucleic acids from complex matrices such as soil and blood, the dPCR quantification can be biased due to the presence of inhibitory compounds. Here, we present how certain inhibitors disturb dPCR quantification and suggest solutions to these problems. Furthermore, we use real-time PCR, dPCR and isothermal titration calorimetry as tools to elucidate the mechanisms underlying the PCR inhibition. The impact of impurities on dPCR quantification was studied using humic acid as a model inhibitor. We show that the inhibitor-tolerance differs greatly for three different DNA polymerases, illustrating the importance of choosing a DNA polymerase-buffer system that is compatible with the samples to be analysed. Various inhibitory-substances from blood were found to disturb the system in different ways. For example, hemoglobin was found to cause quenching of fluorescence and a dramatic decrease of the number of positive reactions, leading to an underestimation of DNA quantity. IgG caused an increased number of late-starters. The system was more susceptible to inhibition by IgG when single-stranded DNA was used as template, compared with double-stranded DNA. By understanding more about the mechanisms of PCR inhibitors it will be possible to design more optimal PCR chemistries, improving dPCR detection and quantification.

Ämnesord

NATURVETENSKAP  -- Biologi -- Biokemi och molekylärbiologi (hsv//swe)
NATURAL SCIENCES  -- Biological Sciences -- Biochemistry and Molecular Biology (hsv//eng)
SAMHÄLLSVETENSKAP  -- Juridik -- Juridik och samhälle (hsv//swe)
SOCIAL SCIENCES  -- Law -- Law and Society (hsv//eng)

Publikations- och innehållstyp

vet (ämneskategori)
kon (ämneskategori)

Till lärosätets databas

Kungliga biblioteket hanterar dina personuppgifter i enlighet med EU:s dataskyddsförordning (2018), GDPR. Läs mer om hur det funkar här.
Så här hanterar KB dina uppgifter vid användning av denna tjänst.

 
pil uppåt Stäng

Kopiera och spara länken för att återkomma till aktuell vy