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Nat Methods ; 20(1): 65-69, 2023 01.
Artículo en Inglés | MEDLINE | ID: mdl-36550273

RESUMEN

Ultraviolet crosslinking and immunoprecipitation (CLIP) methodologies enable the identification of RNA binding sites of RNA-binding proteins (RBPs). Despite improvements in the library preparation of RNA fragments, the enhanced CLIP (eCLIP) protocol requires 4 days of hands-on time and lacks the ability to process several RBPs in parallel. We present a new method termed antibody-barcode eCLIP that utilizes DNA-barcoded antibodies and proximity ligation of the DNA oligonucleotides to RBP-protected RNA fragments to interrogate several RBPs simultaneously. We observe performance comparable with that of eCLIP with the advantage of dramatically increased scaling while maintaining the same material requirement of a single eCLIP experiment.


Asunto(s)
ARN , Transcriptoma , ARN/genética , Sitios de Unión , Unión Proteica , Proteínas de Unión al ARN/metabolismo , Anticuerpos/química , Inmunoprecipitación
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