T-9 peptide
Ref. 3D-CRB1001633
| 1mg | 271.00 € | ||
| 500µg | 198.00 € |
Product Information
- H-SKTFNTHPQSTP-OH
Duchenne muscular dystrophy is a severe muscle wasting X-linked genetic disease cause by mutations in the gene encoding the muscle structural protein, dystrophin. Exon skipping therapy remains a key approach for treatment of DMD but still requires considerable research to improve efficient and specific delivery of molecules to myofibers. Use of a phage library identified this sequence as having a high affinity for myofibers. Conjugation of this peptide to novel DMD molecules could provide the insights needed in the field.
Chemical properties
Technical inquiry about: 3D-CRB1001633 T-9 peptide
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