In addition, PCR can detect small deletions and can specifically localize the regions contained in the deletion. |
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Different numbers of PCR cycles were performed to determine the logarithmic phase of the reaction. |
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We performed PCR on wild-type mouse genomic DNA to amplify sequences flanking transposon insertion sites for use as probes. |
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Pools of all sizes tested gave positive signals indicating that all the pool sizes are amenable for the PCR assay. |
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Where appropriate a master mix of PCR reaction components was made and aliquoted into individual reactions. |
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Similar results were obtained from at least two independent PCR assays of two independent chromatin isolations. |
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The DNA sample from the patient is labeled and amplified by PCR and then added to the filter paper. |
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The positions of primers used for PCR amplification and sequencing and the diagnostic PstI site are indicated. |
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The junctions of the rearrangements were then amplified by PCR and sequenced to reveal the breakpoints. |
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Three randomly picked clones from each PCR reaction were eventually sequenced. |
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In cases where PCR recombination was suspected to occur uniquely in a single clone, the mosaic clone was removed from consideration. |
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Thirty microlitres of PCR product was loaded on 1.5 per cent agarose gel electrophoresed and stained with ethidium bromide. |
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We performed two experiments in order to eliminate the possibility that the recombination we observed was an artifact of the PCR reaction. |
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Arrows below the gene map indicate primers used in PCR analysis of the P-element insertions. |
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After genetic isolation of P insertion chromosomes, the flanking sequences were obtained by inverse PCR and sequenced. |
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The two loci marked with a number sign indicate those analyzed by quantitative PCR in the previous study. |
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Immunoprecipitation, deproteinization, and PCR were performed as described. |
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Species-specific primers were developed to amplify the PBP gene region, and three individuals were sequenced directly from these PCR products. |
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Their portability from bread wheat to durum wheat has been verified by PCR amplification in durum wheat, using primers defined for bread wheat under the same PCR conditions. |
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After construction of the chimeras by overlapping PCR, all of the chimeric genes were cloned into integrating vectors under control of the SEC9 or the SPO20 promoter. |
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The assay was based on the incorporation of digoxigenin labeled dUTP and a biotin labeled primer specific for Shiga toxin genes during PCR amplification. |
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This seems particularly likely in the patient who had an old, inactive hip joint tuberculosis and a false-positive PCR test result from the knee joint sample in this study. |
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In 17 of 19 cases PCR yielded nonspecific products or failed. |
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The PCR products were analyzed by electrophoresis on agarose gels containing ethidium bromide and were photographed under ultraviolet transillumination. |
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The fourth case failed to demonstrate clonality by flow cytometry and PCR owing to a lack of viable cells and lack of amplification, respectively. |
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The EBV genome and clonality were detected by Southern blot and PCR assay. |
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Probes were obtained by PCR amplification of the indicated loci. |
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These instruments also have built-in fluorimeters that detect fluorescence emitted from nucleic probes annealed to target DNA at the conclusion of each PCR cycle. |
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In conclusion, PCR can be used as an additional test for detecting M. tuberculosis in patients with tubercular pleuritis because conventional methods have low sensitivity. |
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Absence of the wild-type gene was also verified by PCR at this point. |
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For MHC sampling, degenerate PCR primers were designed from an alignment of guppy, topminnow, cichlid, and bass Mhc class II B sequences found in GenBank. |
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Detection of Chlamydia trachomatis from urine specimens by PCR in women with cervicitis. |
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We also performed PCR to amplify a portion of D loop using the same primers and thermoprofile used by Bozarth et al. |
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It is classified into PCR, sequencing, northern blotting, southern blotting, molecular cloning, and other nucleic acid applications. |
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Purity of DNA was checked and contamination by bacterial DNA was ruled out by performing a 16S ribosomal DNA PCR for eubacteria. |
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Real-time PCR for detection and quantification of the protistan parasite Perkinsus marinus in environmental waters. |
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The restriction enzyme digestion of all the PCR products, as visualized in Agarose gel electrophoresis after ethidium bromide staining. |
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For the analysis of the COL4A4 gene, all the exons including splicing sites were amplified by PCR and screened by direct sequencing analysis. |
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Diagnostic immunohistochemistry and PCR are available in only a few reference laboratories. |
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A repeat vitreous tap in April 2011 showed a positive PCR for VZV in addition to CMV and she received 2 weeks of intravenous acyclovir. |
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A multiplex PCR assay was used with primers used for the K99, Sta, Stx1, Stx2, intimin, and the F41 fimbrial subunit genes. |
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On PCR testing of the ingluvies and surrounding tissues, results were positive for Aspergillus species. |
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The extracted DNA was then subjected to 18S rDNA PCR for free-living amebas as described by Tsvetkova et al. |
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Use of real-time PCR for determining copy number and zygosity in transgenic plants. |
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Multiplex PCR for typing and subtyping influenza and respiratory syncytial viruses. |
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Advantages of real-time PCR assay for diagnosis and monitoring of canine leishmaniosis. |
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All fungi were identified as Ascomycetes based on their ITS region of rRNA using PCR followed by DNA sequencing. |
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Multiplex PCR targeting tpi, tcdA, and tcdB genes for toxigenic culture of Clostridium difficile. |
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The successful PCR amplicons were sent for direct sequencing to the Chromous Biotech Pvt. |
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As such, FISH and PCR complement each other and are both essential for detecting t translocation. |
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Recently, 3rd generation PCR technology, named digital PCR, has developed for directly quantifying and clonally amplifying nucleic acids. |
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Detection of Neisseria meningitides in clinical samples by a duplex real-time PCR targeting the porA and ctrA genes. |
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Microarrays, PCR and RNAi, have been gaining prominence in this microtechnology era. |
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To monitor the quality of DNA extraction and potential PCR inhibition, we added low concentrations of phocine herpesvirus to the lysis buffer. |
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In addition to identifying uncultivable organisms, PCR and RT-PCR assays have the advantage of obtaining quick results, often within 24 hours. |
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The 5' nuclease assay uses fluorogenic allele-specific detection probes that allow PCR amplification and allele detection in a single procedure. |
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Comparison of PCR assay and cytotaxonomy for identification of Anopheles fluviatilis sibling species. |
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Real-time PCR assay for detection and relative quantification of Liocarcinus depurator larvae from plankton samples. |
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The web site walks the researcher through the design of the primers needed for conducting allele-specific PCR against the SNP target of interest. |
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The GSTP1 polymorphism was determined by a tetra-primer amplification refractory mutation system PCR as described in an earlier study. |
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Simple and sensitive detection of mutations in the ras proto-oncogenes using PNA-mediated PCR clamping. |
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Development of novel real-time PCR assays for detecting DNA virus infections in psittaciform birds. |
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Identification of Pythium insidiosum by nested PCR in cutaneous lesions of Brazilian horse and rabbits. |
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One strand is usually overproduced by asymmetric PCR to allow intramolecular hairpin formation and genotyping using the excess strand. |
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Serotype-specific detection of dengue viruses in a fourplex real-time reverse transcriptase PCR assay. |
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Last month's Primer dealt with endpoint product detection methods for PCR, with a primary focus on the agarose gel electrophoresis method. |
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The axenicity of the filtered samples was proven by PCR using the primers and cycling conditions described by Spoerner et al. |
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The research will use Orion's proprietary DNA methylation technologies, including MethylScope microarrays and MethylScreen PCR assays. |
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These parameters further support the usefulness of the new heptaplex PCR assay in routine clinical diagnosis and infection control. |
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A significant proliferation of the infectious agent does not occur, this limits the ability of PCR to detect the presence of any bacteria. |
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A real-time RT quantative PCR for the detection of bovine ephemeral fever virus. |
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The high degree of variability posed problems for the design of PCR and sequencing primers. |
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Repetitive element PCR fingerprinting using enterobacterial repetitive intergenic consensus primers is not necessarily directed at ERIC elements. |
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To enhance the samarium signal, especially after the blood-spot PCR, polyethylene glycol and dextran sulfate additives were tested. |
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The assay is based on a combination of multiplex PCR and biochip array hybridization. |
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Thousands of samples can now be sorted by this PCR alone without needing Southern blot or capillary electrophoresis. |
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But prior to any PCR amplification steps, all DNA fragment ends are ligated to a pair of adaptors chosen at random from a total set of 9,216 molecular indices. |
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The eluent typically flows to a PCR amplification zone after purification. |
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Results of reverse transcription PCR were negative for WNV and members of genus Flavivirus in serum and CSF samples taken 4 days after disease onset. |
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We describe 2 cases of serogroup C meningococcal disease diagnosed post mortem by PCR from vitreous humor and immunohistochemical staining of tissues collected at autopsy. |
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Where possible, archived DNA from family members was tested with PCR, restriction endonuclease or sequence analysis for the putative change identified in the proband. |
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Direct PCR detection of phytoplasmas in experimentally infected insects. |
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Actually, when the STR loci in question are on an autosome as most are, then a human DNA sample will have two loci copies, so two PCR products will be amplified. |
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Like PCR, however, this pairing is driven by sequence homology, and if the correct matching target sequence is not present, the T7-tagged primer will not successfully anneal. |
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Digital PCR is a novel application of the now 30-year-old PCR technology. |
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Lymph node sampling by fine-needle aspiration showed caseating granulomatous inflammation, but AFB and fungal smears and Mycobacterium tuberculosis PCR results were negative. |
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Techniques such as PCR, DNA microarray, DNA sequencing, mass spectrometry and flow cytometry have driven discoveries that have changed our understanding of the world. |
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The clone libraries of the spirochete-specific PCR products showed that clones retrieved from all investigated bivalve species matched sequences of the spirochetal group. |
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In particular, advanced real time PCR technology is increasingly being used in the rapid detection of food pathogens and spoilage micro-organisms. |
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Bacterial mycobacterial and mycotic cultures of the CSF, PCR analysis for Herpes Simpelx Virus and neurotropic viruses in the blood and CSF were negative. |
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Briefly, red blood cells are first lysed in a large volume, which dilutes the hemoglobin and anticoagulants to an extent that PCR and post-PCR treatments are not inhibited. |
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The present study aims to design and test a nested PCR system that targets the COI gene in order to identify the RTB from the four other beetles in the bark beetle family. |
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As a result, extension rates better reflect the kinetics seen in PCR with processive extension of a defined template for more reproducible activity measurements. |
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An aliquoted FOXL2 PCR product was used for bidirectional DNA sequencing. |
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Reverse transcription PCR was conducted using a primer pair targeting nonstructural protein 1 of Getah virus by using the RNA extracted from the blood samples. |
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All strains were positive for fcpA, tcpI, acfB, toxT, ctxA, zot, and ToxR genes, as well as for the O139-specific genomic DNA in DNA probe or PCR assays. |
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Third, the essential tools for directing PCR, primers, are derived from the genomes of infectious agents, and with time those genomes will be known, if they are not already. |
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Oligonucleotide primers for PCR amplification of coelomate introns. |
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The only remaining blockades to the use of PCR as a standard tool of diagnosis are in its cost and application, neither of which is insurmountable. |
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