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ADAMTS2 peptide
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| Post Date: | Apr 07,2017 |
| Expiry Date: | Apr 07,2018 |
| Detailed Description: |
This gene encodes a member of the ADAMTS (a disintegrin and metalloproteinase with thrombospondin motifs) protein family. Members of the family share several distinct protein modules, including a propeptide region, a metalloproteinase domain, a disintegrin-like domain, and a thrombospondin type 1 (TS) motif. Individual members of this family differ in the number of C-terminal TS motifs, and some have unique C-terminal domains. The enzyme encoded by this gene excises the N-propeptide of type I, type II and type V procollagens. Mutations in this gene cause Ehlers-Danlos syndrome type VIIC, a recessively inherited connective-tissue disorder. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2010] http://www.creative-diagnostics.com/ADAMTS2-peptide-176507-427.htm
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| Company: | Creative Diagnostics [ United States ] |
| Contact: | Emily Dean |
| Tel: | 1-631-619-7922 |
| Fax: | |
| Email: | contact@creative-diagnostics.com |
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