To evaluate some synthetic catalysts that mimic ribonuclease, a quantitative assay has been developed that measures the number of phosphate diester bonds cleaved in a polymeric RNA substrate. This assay involves determining the number of 5'-oligonucleotide termini produced during the cleavage, using
An assay for the endonucleolytic cleavage of RNA to large oligonucleotides
โ Scribed by M.V. Berridge; A.I. Aronson
- Publisher
- Elsevier Science
- Year
- 1973
- Tongue
- English
- Weight
- 596 KB
- Volume
- 53
- Category
- Article
- ISSN
- 0003-2697
No coin nor oath required. For personal study only.
โฆ Synopsis
A rapid assay for endonuclease activity which cleaves high-molecularweight RNA to acid-precipitable fragments has been developed. RNA is covalently coupled to beaded agarose under conditions that produce relatively few coupling sites. The immobilized RNA can be used qualitatively or semiquantitatively in an assay for endonuclease activity by determining the release of acid-precipitable RNA from the complex. This assay is compared to one employing separation of degraded RNA by gel electrophoresis.
๐ SIMILAR VOLUMES
The 5'-proximal trp leader RNA segment (about 5S) decays at 2 to 3 times slower rates than the distal trp mRNA sequence. This has been demonstrated by employing the deletion mutants which lack a large portion of the structural genes but retain the promoter-proximal region of the trp operon. Relative
A reliable, simple, and cost-effective method for the immobilization of relatively short ( \(12-30\) mer) oligonucleotide probes to 96 -well polystyrene plates was required in our laboratory for use in DNA hybridizationbased assays. We compared three different approaches to achieve this immobilizati
The previously synthesized, terminally blocked heptapeptide Ac-Aib-ATANP-Aib-Aib-ATANP-Aib- Aib-OMe (1a), where ATANP is (S)-2-amino-3-[1- (1,4,7-triazacyclononane)]propanoic acid and Aib is โฃ-aminoisobutyric acid, which is soluble in neutral water where it largely adopts a 3 10 -helical conformatio