Results 61 to 70 of about 40,087 (166)
Real-Time PCR Assay for Quantitative Mismatch Detection
We describe here a quantitative realtime PCR assay for the detection of single-base-pair differences that does not require fluorescently labeled gene-specific probes or complicated primer combinations.
L. Shively +5 more
doaj +1 more source
Reactivity of Ferrocenylcarbodiimide with DNA Duplex Containing Single-mismatched Base Pairs
Ferrocenylcarbodiimide (1), which is known to react with a guanine (G) or thymine (T) base of single stranded DNA, was allowed to react with DNA duplex having a single mismatched base pair of G-T, T-T, or T-cytosine (C). Electrophoreograms of the reaction mixture showed that 1 could react with G or T base of the mismatched sites on the DNA duplex ...
Kosuke, Mukumoto +4 more
openaire +3 more sources
Effect of Single Mismatches at 3′–end of Primers on Polymerase Chain Reaction
Objective and Method – To investigate the effect of three different mismatches (G/T, G/A or G/G) at the 3•– end of a primer to amplify a 268 bp (base pair) region of the human •–globin gene using different annealing temperatures (45 to 65•C).
Simsek M, Adnan H
doaj
Bioassays based on cellulose paper substrates are gaining increasing popularity for the development of field portable and low-cost diagnostic applications.
Feng Zhou +2 more
doaj +1 more source
Of the DNA bases, the hydrogen bonding characteristics of guanine (G) are complementary only to those of cytidine (C) and, similarly, the hydrogen bonding characteristics of adenine (A) are complementary only to those of thymine (T) (Fig. 1). This is the fundamental basis of Watson-Crick base pairing in DNA and ensures the extremely high fidelity of ...
Leonard, G, Hunter, W, Brown, T
openaire +2 more sources
Constitutional mismatch repair deficiency (CMMRD), caused by bi-allelic germline variants in mismatch repair (MMR) genes, is associated with high cancer incidence early in life.
Dilys D. Weijers +19 more
doaj +1 more source
Muver, a computational framework for accurately calling accumulated mutations
Background Identification of mutations from next-generation sequencing data typically requires a balance between sensitivity and accuracy. This is particularly true of DNA insertions and deletions (indels), that can impart significant phenotypic ...
Adam B. Burkholder +5 more
doaj +1 more source
High fidelity DNA ligation prevents single base insertions in the yeast genome
Finalization of eukaryotic nuclear DNA replication relies on DNA ligase 1 (LIG1) to seal DNA nicks generated during Okazaki Fragment Maturation (OFM). Using a mutational reporter in Saccharomyces cerevisiae, we previously showed that mutation of the high-
Jessica S. Williams +6 more
doaj +1 more source
Background The polymerase chain reaction (PCR) is commonly used to detect the presence of nucleic acid sequences both in research and diagnostic settings.
Powers Kristy M +6 more
doaj +1 more source
Background: DNA hybridization is at the basis of most current technologies for genotyping and sequencing, due to the unique properties of DNA base-pairing that guarantee a high grade of selectivity.
Maryse D. Nkoua Ngavouka +5 more
doaj +1 more source

