anti-ADAM17 (human), mAb (rec.) (blocking) (D1(A12)) (preservative free)
|Synonyms||TNF-α-converting Enzyme; Disintegrin and Metalloproteinase Domain-containing Protein 17; CD156b|
|Product Type||Monoclonal Antibody|
|Immunogen/Antigen||Recombinant human ADAM17 (TACE) ectodomain tagged to biotin.|
Functional Application (Blocking): Inhibits ADAM17 activity at 30μg/ml (200nM).
Recognizes the catalytic and non-catalytic domain of human ADAM17 (TACE) through its variable light (VL) domain and variable heavy (VH) domain, respectively. Does not bind recombinant mouse ADAM17 ectodomain.
|Purity Detail||Protein A/G-affinity purified.|
|Formulation||Liquid. In PBS.|
|Other Product Data||
This cross-domain human antibody is a selective ADAM17 (TACE) antagonist and provides a unique alternative to small molecule metalloprotease inhibition. ADAM multidomain topology was exploited by first isolating an inhibitory human antibody (D1) that bound ADAM17-specific non-catalytic regions exclusively through its variable heavy (VH) domain. A D1-VH biased scFv phage-display library was then used to selectively isolate a new variable light (VL) chain that could simultaneously bind to the ADAM17 catalytic domain.
|Accession Number||UniProt ID P78536|
|Shipping and Handling|
|Short Term Storage||+4°C|
|Long Term Storage||-20°C|
|Handling Advice||Avoid freeze/thaw cycles.|
|Use/Stability||Stable for at least 1 year after receipt when stored at -20°C.|
|Product Specification Sheet|
ADAM17 (Disintegrin and metalloproteinase domain-containing protein 17), also called TACE (Tumor necrosis factor-α-converting enzyme) is the prototype of the ADAM family of ectodomain shedding proteases (sheddase). ADAM17 is understood to be involved in the processing of TNF-α at the surface of the cell and from within the intracellular membranes of the trans-Golgi network. This process involves the cleavage and release of a soluble ectodomain from membrane-bound pro-proteins (such as pro-TNF-α) and is of known physiological importance. ADAM17 is responsible for the processing of a diverse variety of membrane-anchored cytokines, cell adhesion molecules, receptors, ligands and enzymes, including cleaving epidermal growth factor receptor (EGFR) ligands and extracellular Notch1. The proteolytic cleavage is an indispensable activation event for many of these substrates, ADAM17 has emerged as an attractive therapeutic target for the treatment of inflammatory diseases (e.g. rheumatoid arthritis) or inflammation associated cancer.
- Cross-domain inhibition of TACE ectodomain: C.J. Tape, et al.; PNAS 108, 5578 (2011)
- Anti-tumour effects of a specific anti-ADAM17 antibody in an ovarian cancer model in vivo: F.M. Richards, et al.; PLoS One e40597 (2012)
- iRHOM2 is a critical pathogenic mediator of inflammatory arthritis: P.D. Issuree, et al.; J. Clin. Invest. 123, 928 (2013)
- NK cell CD16 surface expression and function is regulated by a disintegrin and metalloprotease-17 (ADAM17): R. Romee, et al.; Blood 121, 3599 (2013)
- Development of a 'mouse and human cross-reactive' affinity-matured exosite inhibitory human antibody specific to TACE (ADAM17) for cancer immunotherapy: H.F. Kwok, et al.; Protein Eng. Des. Sel. 27, 179 (2014)
- Targeting the sheddase activity of ADAM17 by an anti-ADAM17 antibody D1(A12) inhibits head and neck squamous cell carcinoma cell proliferation and motility via blockage of bradykinin induced HERs transactivation: Y. Huang, et al.; Int. J. Biol. Sci. 10, 702 (2014)
- Targeting ADAM-17 with an inhibitory monoclonal antibody has antitumour effects in triple-negative breast cancer cells: F. Caiazza, et al.; Br. J. Cancer 112, 1895 (2015)
- Recent advances in the field of anti-cancer immunotherapy: H. Neves & H.F. Kwok; BBA Clinical 3, 280 (2015) (Review)