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In the A/T site, the A-site half resides in the small ribosomal subunit where the mRNA decoding site is located. The mRNA decoding site is where the mRNA codon is read out during translation. The T-site half resides mainly on the large ribosomal subunit where EF-Tu or eEF-1 interacts with the ribosome.
Small RNA that is activated by SgrR in Escherichia coli during glucose-phosphate stress shRNA: short hairpin RNA - siRNA: small interfering RNA - SL RNA spliced leader RNA multiple families: SmY RNA: mRNA trans-splicing RF01844: Small nuclear RNAs found in some species of nematode worms, thought to be involved in mRNA trans-splicing snoRNA ...
Competitive RT-PCR technique is used for absolute quantification. It involves the use of a synthetic “competitor” RNA that can be distinguished from the target RNA by a small difference in size or sequence. It is important for the design of the synthetic RNA be identical in sequence but slightly shorter than the target RNA for accurate results.
RNA-Seq methodology has constantly improved, primarily through the development of DNA sequencing technologies to increase throughput, accuracy, and read length. [61] Since the first descriptions in 2006 and 2008, [40] [62] RNA-Seq has been rapidly adopted and overtook microarrays as the dominant transcriptomics technique in 2015. [63]
Reverse transcription loop-mediated isothermal amplification (RT-LAMP) is a one step nucleic acid amplification method to multiply specific sequences of RNA. It is used to diagnose infectious disease caused by RNA viruses. [1] It combines LAMP [2] DNA-detection with reverse transcription, making cDNA from RNA before running the reaction. [3]
Transfer RNA. The T-arm or T-loop is a specialized region on the tRNA molecule which acts as a special recognition site for the ribosome to form a tRNA-ribosome complex during protein biosynthesis or translation (biology). The T-arm has two components to it; the T-stem and the T-loop.
RNA sequencing is a next-generation sequencing technology; as such it requires only a small amount of RNA and no previous knowledge of the genome. [3] It allows for both qualitative and quantitative analysis of RNA transcripts, the former allowing discovery of new transcripts and the latter a measure of relative quantities for transcripts in a ...
The presence of this functional group causes the helix to mostly take the A-form geometry, [11] although in single strand dinucleotide contexts, RNA can rarely also adopt the B-form most commonly observed in DNA. [12] The A-form geometry results in a very deep and narrow major groove and a shallow and wide minor groove. [13]