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Creative Biolabs

NoGeneST™ DMD-ASO, Antisense Oligonucleotide

[CAT#: NRYF-0625-XY12]

Target:
DMD

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Product Overview

Description

DMD-ASO is a non-charged antisense oligonucleotide that targets exon 51 of the dystrophin gene by altering RNA splicing.

Species

Human

Applications

Our DMD-ASO is designed to target the Duchenne Muscular Dystrophy (DMD) gene. While primarily associated with muscle pathology, it also aids in exploring the impact of DMD gene dysregulation on neuromuscular junction function and potential secondary effects on the nervous system, providing insights into the broader disease mechanisms and possible neurological interventions.

Relevant Diseases

Duchenne muscular dystrophy
Properties

Appearance

Solid

Shipping

Room temperature

Storage

Store at -20°C, sealed and away from moisture.
In solvent, store at -80°C for up to 6 months, or -20°C for up to 1 month (sealed and away from moisture).

Research Use Only

For research use only.
Target Details

Target

DMD

Official Name

Dystrophin

Full Name

Dystrophin

Alternative Names

Muscular Dystrophy, Duchenne And Becker Types; Mental Retardation, X-Linked; Mutant Dystrophin; CMD3B
Publications

Publications (0)

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For Research Use Only. Not For Clinical Use.
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