ADAMTS2

gene product
ADAM-TS2, ADAMTS-3, hPCPNI, NPI, PCINP
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 encoded preproprotein is proteolytically processed to generate the mature procollagen N-proteinase. This proteinase excises the N-propeptide of the fibrillar procollagens types I-III and type V. Mutations in this gene cause Ehlers-Danlos syndrome type VIIC, a recessively inherited connective-tissue disorder. Alternative splicing results in multiple transcript variants, at least one of which encodes an isoform that is proteolytically processed. [provided by RefSeq, Feb 2016]
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antibodies-online
40 antibodies
Invitrogen Antibodies
7 antibodies
Biorbyt
20 antibodies
Affinity Biosciences
1 antibody
LifeSpan BioSciences, Inc.
50 antibodies
Abnova Corporation
3 antibodies
Novus Biologicals
3 antibodies
Atlas Antibodies
1 antibody
Boster Biological Technology
1 antibody
NSJ Bioreagents
1 antibody
Abgent
1 antibody
NovoPro Bioscience Inc.
1 antibody
Aviva Systems Biology
1 antibody
OriGene
3 antibodies
MyBioSource
7 antibodies
Creative Biolabs
4 antibodies
GeneTex
3 antibodies
Abbkine Scientific Co.Ltd.
1 antibody
Bioworld Technology, Inc
1 antibody
Creative Diagnostics
3 antibodies
Abbiotec
1 antibody
Acris Antibodies GmbH
1 antibody
St John's Laboratory
1 antibody
United States Biological
14 antibodies
Sigma-Aldrich
4 antibodies
Rockland Immunochemicals, Inc.
1 antibody
GenWay
2 antibodies