E-AB-19434
ADAMTS2 Polyclonal Antibody
Size
£106.20
Was £118.00
- SKU:
- E-AB-19434
- Additional Names:
- A disintegrin and metalloproteinase with thrombospondin motifs 2,A disintegrin like and metalloprotease (reprolysin type) with thrombospondin type 1 motif 2,ADA,ADAM TS 2,ADAM TS2,ADAM metallopeptidase with thrombospondin type 1 motif 2,ADAM-TS 2,ADAM-TS2
- Application:
- IHC
- Concentration:
- 1.32 mg/ml
- Purification:
- Affinity Purified
- Storage Conditions:
- -20[o]C Avoid freeze/thaw cycles.
- Supplier:
- Elabscience
- Host:
- Rabbit
- Reactivities:
- Human, Mouse
- Buffer:
- Phosphate buffered solution, pH 7.4, containing 0.05% stabilizer and 50% glycerol.
- Immunogen:
- Synthetic peptide of human ADAMTS2
- Uniprot:
- O95450
- Synonyms:
- A disintegrin and metalloproteinase with thrombospondin motifs 2;a disintegrin-like and metalloprotease (reprolysin type) with thrombospondin type 1 motif, 2;ADAM-TS2;ADAMTS-2;ADAMTS-3;EDSDERMS;NPI;PC I-NP;PCI-NP;PCINP;PCPNI;PNPI;procollagen I N-proteinase;procollagen I/II amino propeptide-processing enzyme;procollagen N-endopeptidase
- Extra Details:
- 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.
- Shipping Conditions:
- Blue Ice