Antisense Rna

Antisense RNA is an RNA molecule with a sequence complementary to a target RNA, enabling precise regulation of gene expression in cells. By base-pairing with messenger RNA, it can block ribosome access, alter RNA stability, promote degradation, or influence processing and transcription, depending on the cellular context. These regulatory molecules occur naturally in bacteria, plants, and animals and can also be designed as experimental tools or therapeutic agents. Studying antisense RNA helps clarify post-transcriptional control, microbial adaptation, and disease-related gene regulation, while supporting approaches such as gene silencing and targeted treatment development.

Antisense Rna - Related Videos

Research

JoVE Journal - Biology

Microinjection of mRNA and Morpholino Antisense Oligonucleotides in Zebrafish Embryos.

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Cited by 86 •

2009

Microinjection is a well-established and effective method for introducing foreign substances into fertilized zebrafish embryos. Here, we demonstrate a robust microinjection technique for performing mRNA overexpression, and morpholino oligonucleotide gene knockdown studies in zebrafish.

Research

JoVE Journal - Medicine
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Multi-exon Skipping Using Cocktail Antisense Oligonucleotides in the Canine X-linked Muscular Dystrophy

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Cited by 23 •

2016

Exon skipping is currently a most promising therapeutic option for Duchenne muscular dystrophy (DMD). To expand the applicability for DMD patients and to optimize the stability/function of the resulting truncated dystrophin proteins, a multi-exon skipping approach using cocktail antisense oligonucleotides was developed and we demonstrated systemic dystrophin rescue in a dog model.

Depletion of Ribosomal RNA for Mosquito Gut Metagenomic RNA-seq

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Cited by 20 •

2013

A ribosomal RNA (rRNA) depletion protocol was developed to enrich messenger RNA (mRNA) for RNA-seq of the mosquito gut metatranscriptome. Sample specific rRNA probes, which were used to remove rRNA via subtraction, were created from the mosquito and its gut microbes. Performance of the protocol can result in the removal of approximately 90-99% of rRNA.

Whole Mount RNA Fluorescent in situ Hybridization of Drosophila Embryos

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Cited by 22 •

2013

Here we describe a whole-mount fluorescent in situ hybridization (FISH) protocol for determining the expression and localization properties of RNAs expressed during embryogenesis in the fruit fly, Drosophila melanogaster.

Research

JoVE Journal - Biology
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Chromatin Isolation by RNA Purification (ChIRP)

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Cited by 380 •

2012

ChIRP is a novel and rapid technique to map genomic binding sites of long noncoding RNAs (lncRNAs). The method takes advantage of the specificity of anti-sense tiling oligonucleotides to allow the enumeration of lncRNA-bound genomic sites.

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