文献支持ADAMTS2 Polyclonal Antibody_货号:E-AB-19434_多克隆抗体

Verified Samples in IHC:Human tonsil

IHC 1:30-1:150, ELISA 1:5000-1:10000

Polyclonal

IgG

Synthetic peptide of human ADAMTS2

ADAMTS2

A disintegrin and metalloproteinase with thrombospondin motifs 2;A disintegrin like and metalloprotease (reprolysin type) with thrombospondin type 1 motif 2;ADAM metallopeptidase with thrombospondin type 1 motif 2;ADAM TS 2;ADAM TS2;ADAM-TS 2;ADAM-TS2;ADAMTS 3;ADAMTS-2;ADAMTS2;ATS2;EC 3.4.24.14;EDS VIIB;EDS VIIC;hPCPNI;NPI;PC I NP;PC I-NP;PCINP;PCPNI;pNPI;Procollagen I N proteinase;Procollagen I N-proteinase;Procollagen I/II amino propeptide processing enzyme;Procollagen I/II amino propeptide-processing enzyme;Procollagen N endopeptidase;Procollagen N-endopeptidase抗体

O95450

Secreted>extracellular space>extracellular matrix.

1.32 mg/mL

Store at -20°C Valid for 12 months. Avoid freeze / thaw cycles.

PBS with 0.05% NaN3 and 40% Glycerol,pH7.4

Antigen affinity purification

Cancer; Cell Biology; Cardiovascular; Signal Transduction

Unconjugated

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.