Results 131 to 140 of about 14,674 (226)
Bacteria and Archaea encode clustered, regularly interspaced, short palindromic repeat (CRISPR) systems to confer adaptive immunity to invasive viruses and plasmids.
Hallstrøm, Søren +5 more
core +1 more source
Deep learning enhancing guide RNA design for CRISPR/Cas12a‐based diagnostics
Rapid and accurate diagnostic tests are fundamental for improving patient outcomes and combating infectious diseases. The Clustered Regularly Interspaced Short Palindromic Repeats (CRISPR) Cas12a‐based detection system has emerged as a promising solution
Baicheng Huang +16 more
doaj +1 more source
EcCas6e-based antisense crRNA for gene repression and RNA editing in microorganisms
Abstract Precise gene regulation and programmable RNA editing are vital RNA-level regulatory mechanisms. Gene repression tools grounded in small non-coding RNAs, microRNAs, and CRISPR-dCas proteins, along with RNA editing tools anchored in Adenosine Deaminases acting on RNA (ADARs), have found extensive application in molecular biology ...
Mutong Li +7 more
openaire +2 more sources
Efficient Genome Editing Using ‘NanoMEDIC’ AsCas12a-VLPs Produced with Pol II-Transcribed crRNA
Virus-like particles (VLPs) are an attractive vehicle for the delivery of Cas nuclease and guide RNA ribonucleoprotein complexes (RNPs). Most VLPs are produced by packaging SpCas9 and its sgRNA, which is expressed from the RNA polymerase III (Pol III ...
Dmitriy V. Mazurov +3 more
core +1 more source
Clustered regularly interspaced short palindromic repeats (CRISPR) technology has revolutionized creating targeted genetic variation in crops. Although CRISPR enzymes have been reported to have high sequence‐specificity, careful design of the editing ...
Linda Rymarquis +6 more
doaj +1 more source
(A) Whole-mount in situ hybridization with an epdr1 probe. (B) An uninjected embryo. (C) The embryo injected two crRNAs (epdr1-crRNA; 25 pg + Mbait-crRNA; 25 pg), tracrRNA (100 pg) and Mbait-hs-eGFP (25 pg) with Cas9 protein (400 pg).
Satoshi Ota (154675) +4 more
core +1 more source
Binding Data for Cas9, dmCas9, and crRNA Substrates.
aReported as the average and standard error of the mean from 2–3 independent experiments.bCalculated by dividing each Kd value by the Kd for Cas9:cr20:tracrRNA:p53[Exon 7].Binding Data for Cas9, dmCas9, and crRNA Substrates.
Hisashi Miura (638238) +7 more
core +1 more source
Structural basis for target DNA cleavage and guide RNA processing by CRISPR-Casλ2
RNA-guided CRISPR-Cas nucleases are widely used as versatile genome-engineering tools. Among the diverse CRISPR-Cas effectors, CRISPR-Casλ—also referred to as Cas12n—is a recently identified miniature type V nuclease encoded in phage genomes.
Satoshi N. Omura +14 more
doaj +1 more source
Developing a one-pot assay is a critical strategy for enhancing the applicability of CRISPR-based molecular diagnostics; however, it is hindered by CRISPR cleavage interfering with nucleic acid amplification templates. Photo-regulation strategies provide
Tian Tian +10 more
doaj +1 more source
CRISPR-associated (Cas) protein systems have been increasingly incorporated in nucleic-acid diagnosis. CRISPR/Cas12a can cleave single-stranded DNA (ssDNA) after being guided to the target double-stranded DNA (dsDNA) with crRNA, making it a specific tool
He Meng (33363) +8 more
core +1 more source

