We performed RNA-seq in the root tips of two genotypes of bermudagrass, which had different root growth characters and salt tolerance.
Since EpCAM RNA aptamer was shown to get internalized by endocytosis, it would be capable of delivering siRNA into the cell upon chimerization.
Using a technique adapted from plant virology, the samples were freeze dried, homogenized in a genogrinder and thereafter, RNA was extracted according to the manufacturer’s manual (for details see [13 ]).
Particularly interesting is the recent finding that its partner protein MTO1 interacts with mitoribosomal proteins in an RNA-independent manner, which suggests that MTO1 helps in the assembly or stability of mitoribosomes.
Total RNA was isolated from a monokaryotic cultures of Phanerochaete chrysosporium,Trametes versicolor, and Gloeophyllum trabeum.
Total RNA was extracted from 69 fresh endometrium samples collected from 21 healthy female dogs during diestrus, 16 CEH, 15 mucometra and 17 pyometra (eight open and nine closed-cervixes).
Notice that LPGM and Mult-GM were designed for data that are approximately Poisson distributed, such as measurements from RNA-sequencing, and multinomially distributed, such as various types of gene variations, respectively.
This means the stem-loop tool—with its base-pairing and nonpairing composition—is relevant to all agents of the current RNA world being active in cellular genomes after transcription.
Various classes of noncoding RNAs target each other for posttranscriptional regulation via alternative splicing, polyadenylation, 5′ capping, nontemplated modifications, and RNA editing.