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samplescausingPCR failures due to inhibition
Such tertiary structure changes could prevent the binding of DNA to the proteincausingthe inhibition of the PCR process
High viral cDNA concentrationledto PCR reaction inhibition
substances that are purified along with the template DNA ( or RNA in the case of RT - PCR reaction(passive) is often caused byInhibition of a PCR reaction
the cereal DNA(passive) caused byPCR reaction inhibition
contaminantscauseinhibition of PCR reaction
by the presence of double stranded RNA / cDNA hybrids remaining after cdna synthesis(passive) caused byreduced PCR inhibition
the presence of double - stranded RNA / cDNA hybrids remaining after cDNA synthesis(passive) caused byreduced PCR inhibition
this tissueresultsin the inhibition of PCR reactions
However , in some cases , it has been observedcan ... causePCR inhibition and removal
DNA strand ... DNAcausesDNA polymerase inhibition
DNA strand breakage ... DNAcausesDNA polymerase inhibition
High enzyme concentrationmay leadto RT - PCR inhibition
the particlescausesdownstream inhibition of PCR
by high genomic DNA load(passive) caused byPCR inhibition
It may therefore be expectedwill causesome inhibition of PCR
the reactioncausinginhibition in PCR
Effectsresultingfrom PCR inhibition
the quantification results ... the primary reverse transcriptioncan resultin the inhibition of PCR
by plant compounds(passive) caused byPCR inhibition
cDNAcan causeinhibition of your PCR.
cDNAcan causeinhibition of your PCR
the inhibitory substances of the extractcausePCR inhibition
Too much cDNAcan causeinhibition of your PCR.
Too much cDNAcan causeinhibition of your PCR
Too much cDNAcan causeinhibition of your PCR.
the problemcausingPCR inhibition
by co - extracted substances(passive) caused byPCR inhibition
the EDTAcausingPCR inhibition
surfacesleadingto PCR inhibition
by environmental contaminants(passive) caused byPCR inhibition
environmental contaminants(passive) caused byPCR inhibition
that impuritiesmight contributeto PCR inhibition
This template sequence can now be usedto designPCR amplicons
by co - extracted impurities(passive) caused byPCR inhibition
nM QDsledto PCR inhibition
complementary(passive) was designedPCR assay
the compounds necessary for room - temperature storagecan causePCR inhibition
by Wang(passive) invented byPCR assay
DNA degradation DNA degradation andcausePCR inhibitors
false negative resultscould have causedfalse negative results
in a PCR product of 703 bp ( fig . 1resultedin a PCR product of 703 bp ( fig . 1
to false negative resultscould leadto false negative results
from something in bloodprobably causedfrom something in blood
in no amplification of the human and male targetsresultingin no amplification of the human and male targets
quantitative PCR resultscould influencequantitative PCR results
the researchersledthe researchers
results(passive) caused byresults
the false - negative results(passive) caused bythe false - negative results
a false - negative response(passive) caused bya false - negative response
in no amplification of the human and male targetsresultingin no amplification of the human and male targets
a false - negative result(passive) caused bya false - negative result
false negatives(passive) caused byfalse negatives
in the generation of multiple fragments of the proberesultsin the generation of multiple fragments of the probe
in this studydesignedin this study
to false negative resultscould leadto false negative results
false negative resultscan causefalse negative results
A real - time quantitative(passive) was designedA real - time quantitative
A quantitative fluorescent(passive) was ... designedA quantitative fluorescent
from the DNA extractionoriginatingfrom the DNA extraction
The real - time(passive) is designedThe real - time
to specifically adesignedto specifically a
degradation of the viral RNAmay have causeddegradation of the viral RNA
in false - negative testscan resultin false - negative tests
A multiplex polymerase chain reaction(passive) was designedA multiplex polymerase chain reaction
from the starting materialoriginatingfrom the starting material
to improved cardiac function and survivalcontributeto improved cardiac function and survival
in false negativescould resultin false negatives
to quantify the pathogen in barley tissueswas designedto quantify the pathogen in barley tissues
for detection of and discrimination between B19 computer Vicrivirocdesignedfor detection of and discrimination between B19 computer Vicriviroc
for rapid detection of CaPV and tested on sheep experimentally infected with a virulent strain of SPPVdesignedfor rapid detection of CaPV and tested on sheep experimentally infected with a virulent strain of SPPV
to span the desired target sequence , comprehensive resequencing of candidate genomic region using Sanger sequencingdesignedto span the desired target sequence , comprehensive resequencing of candidate genomic region using Sanger sequencing
to span the desired target sequence , comprehensive resequencing of candidate genomic regiondesignedto span the desired target sequence , comprehensive resequencing of candidate genomic region
for the diagnosis of bone and joint infections using prosthetic - joint sonicationdesignedfor the diagnosis of bone and joint infections using prosthetic - joint sonication
with overlapping regions at both flanking ends carrying at least one heterozygous SNPwere designedwith overlapping regions at both flanking ends carrying at least one heterozygous SNP
the development of PCRis leadingthe development of PCR
in the generation of a PCR profile representative of the mRNAsresultingin the generation of a PCR profile representative of the mRNAs
Gene specific primers for quantitative real time(passive) were designedGene specific primers for quantitative real time
The gene - specific primers for real time(passive) were designedThe gene - specific primers for real time
to amplify a product from a given allelic version of the gene , with subsequent detection of an amplified product by any of a number of possible methods includingdesignedto amplify a product from a given allelic version of the gene , with subsequent detection of an amplified product by any of a number of possible methods including