ADAMTS2 Antibody (7G3) Summary
ADAMTS2 (NP_055059, 1112 a.a. ~ 1211 a.a) partial recombinant protein with GST tag.KHNDIDVFMPTLPVPTVAMEVRPSPSTPLEVPLNASSTNATEDHPETNAVDEPYKIHGLEDEVQPPNLIPRRPSPYEKTRNQRIQELIDEMRKKEMLGK
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Antibody reactive against cell lysate and recombinant protein for western blot. It has also been used for ELISA.
Packaging, Storage & Formulations
Aliquot and store at -20C or -80C. Avoid freeze-thaw cycles.
PBS (pH 7.4)
This product is produced by and distributed for Abnova, a company based in Taiwan.
Alternate Names for ADAMTS2 Antibody (7G3)
- A disintegrin and metalloproteinase with thrombospondin motifs 2
- a disintegrin-like and metalloprotease (reprolysin type) with thrombospondintype 1 motif, 2
- ADAM metallopeptidase with thrombospondin type 1 motif, 2
- ADAM-TS 2
- ADAM-TS2EC 18.104.22.168
- EC 3.4.24
- PC I-NP
- Procollagen I N-proteinase
- Procollagen I/II amino propeptide-processing enzyme
- Procollagen N-endopeptidase
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 two transcript variants. The short transcript encodes a protein which has no significant procollagen N-peptidase activity.
This product is for research use only and is not approved for use in humans or in clinical diagnosis. Primary Antibodies are guaranteed
for 1 year from date of receipt.
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