Anti-ADAMTS2 Aptamer SELEX Service(Cat#: CTApt-1207)
This is an aptamer development services to screening aptamers binds to the ADAMTS2 with an affinity of 1nM~1μM.
Specific Inquiry 
Specifications
| Target Category |
Protein |
| Target |
ADAMTS2 |
| Alternative Names |
ADAM Metallopeptidase With Thrombospondin Type 1 Motif 2; Procollagen N-Endopeptidase; Procollagen I N-Proteinase; ADAM-TS2; PCINP; A Disintegrin-Like And Metalloprotease (Reprolysin Type) With Thrombospondin Type 1 Motif, 2; A Disintegrin And Metalloproteinase With Thrombospondin Motifs 2; Procollagen I/II Amino Propeptide-Processing Enzyme; EC 3.4.24.14; ADAMTS-2; ADAMTS-3; PC I-NP; PCPNI; PNPI; NPI; ADAM-TS 2; EC 3.4.24; EDSDERMS; ADAMTS2; PCI-NP; HPCPNI |
| Gene ID |
9509 |
| UniProt ID |
O95450 |
| Target Overview |
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. |
| Chemical Modification |
N/A |
| Type |
DNA |
| Length |
20-80 nt |
| Affinity (Kd) |
1nM~1μM |
| Binding Conditions/Buffer |
PBS; buffer system with Serum; other |
For Research Use Only. Not for Diagnostic or Therapeutic Applications.
