Sentence examples for binding dyes such as from inspiring English sources

In particular, functional groups found within amyloid binding dyes, such as benzothiazole and triazole, can improve inhibition efficacy.

Among the different chemistries used for PCR product detection during amplification, DNA binding dyes such as SYBR® Green I are simple, versatile, and yet highly reliable and least expensive.

Fluorescent nucleic acid binding dyes, such as RiboGreen (Life Technologies), exploit the increase in fluorescence seen on association with RNA.

Quantitative PCR can also use nucleic acid binding dyes such as SYBR® Green or Eva Green® that increase fluorescence in the presence of double-stranded DNA (dsDNA).

Fluorescence light microscopy with differential uptake of fluorescent DNA binding dyes (such as EB/AO staining) is a method of choice for its simplicity, rapidity, and accuracy.

Recent studies have explored the application of DNA binding dyes such as EvaGreen (EG) for the quantitation of single amplicons in a digital PCR format.

Greater concentrations of amyloid-binding dyes such as Congo red and thioflavin T inhibit aggregation of S. cerevisiae cells expressing Als proteins [11], [17].

This belief is supported by the ability some RNA-binding dyes (such as thiazole orange or methylene blue) to stain reticulocytes but not erythrocytes, an observation which forms the basis of the clinical utility of these dyes in distinguishing reticulocytes from mature erythrocytes [5].

Therefore, mature erythrocytes were once thought to lack RNAs and have significantly lower signals from RNA-binding dyes such as methylene blue.

The highly dye-dependent and dye concentration-dependent nature of nonspecific product formation strongly suggest that certain DNA-binding dyes such as SG may have the ability to enhance or promote the formation of nonspecific primer hybridizations, which would otherwise not occur due to imperfect sequence match.

Traditionally, metaphase chromosomes are stained with a DNA-binding dye, such as Giemsa stain, which is taken up readily by gene-poor A,T-rich genomic regions and results in a chromosome-specific banding pattern that can be used to differentiate chromosomes and identify abnormalities.