ADAMTSL2 Polyclonal Antibody, ALEXA FLUOR® 594 Conjugated from Bioss Inc.

Supplier Page

Supplier Page from
Bioss Inc. for
ADAMTSL2 Polyclonal Antibody, ALEXA FLUOR® 594 Conjugated

The ADAMTSL2 Polyclonal Antibody, ALEXA FLUOR® 594 Conjugated from Bioss Inc. is a Rabbit Polyclonal antibody to ADAMTS like 2, and ADAMTSL2. This antibody recognizes Human antigen. The ADAMTSL2 Polyclonal Antibody, ALEXA FLUOR® 594 Conjugated has been validated for the following applications: Immunocytochemistry, Immunofluorescence, Immunohistochemistry, Immunohistochemistry - fixed, and Immunohistochemistry - frozen.

Description

ADAMTS (A Disintegrin And Metalloproteinase Domain with Thrombospondin type 1 Modules) is a family of zinc-dependent proteases that are implicated in a variety of normal and pathological conditions, including arthritis and cancer. ADAMTS protein family members contain an amino-terminal propeptide domain, a metalloproteinase domain, a disintegrin-like domain and a carboxy-terminus that contains a varying number of Thrombospondin type 1 (TSP-1) motifs. ADAMTS-L2 (ADAMTS-like protein 2) is a 951 amino acid secreted protein that is highly expressed in lung, kidney and liver. Mutations in the gene encoding ADAMTS are the cause of geleophysic dysplasia, an autosomal recessive disorder characterized by cardiac vavular anomalies, short stature, thick skin and brachydactyly. In individuals affected with geleophysic dysplasia, there is a significant increase in total active TGF-beta 1 and nuclear locations of p-SAMD2 in fibroblasts. Interestingly, ADAMTS-L2 interacts with LTBP-1, a glycoprotein that is part of the platelet-derived TGF-beta 1 complex