ADAMTS2 peptide

• 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
  

• Company:

  Creative Diagnostics     [ United States ]        

• Contact:

  Emily Dean

• Tel:

  1-631-619-7922

• Fax:

• Email:

  contact@creative-diagnostics.com