This product is an unconjugated, non-therapeutic recombinant analog of the originator antibody izeltabart (the antibody component of izeltabart tapatansine / IMGC936), an investigational anti-ADAM9 agent. It is a human IgG1-kappa recombinant protein built around the ADAM9 target, supplied for research use only (RUO) and not intended for human or veterinary use. Because it is provided unconjugated and payload-free, it serves as a defined tool for studying ADAM9 engagement independent of any cytotoxic warhead. Typical research applications include use as a binding reagent, an isotype-matched positive control, a naked-antibody comparator in antibody-drug conjugate (ADC) development workflows, and a standard in target-expression and internalization assays. The material is offered at research grade with low endotoxin (<1 EU/mg; ultra-low <0.5 EU/mg options), and is available in bulk milligram-to-gram quantities to support scale-dependent in-vitro and preclinical studies. As a biosimilar analog it reproduces the target specificity of the originator for experimental purposes rather than replicating any clinical formulation.
ADAM9 (Q13443; ADAM metallopeptidase domain 9) is a type I transmembrane member of the ADAM (a disintegrin and metalloproteinase) family. It combines a catalytic metalloprotease domain, mediating ectodomain shedding of numerous cell-surface substrates, with a disintegrin domain that supports integrin-dependent cell adhesion. Through these activities ADAM9 participates in cell-cell and cell-matrix interactions, motility, and proteolytic release of membrane proteins involved in tumorigenesis and angiogenesis, including reported substrates such as EPHB4, KDR/VEGFR2, TEK, CD40, VCAM1 and CDH5. ADAM9 is overexpressed across several solid tumor types and its expression often correlates with invasiveness and poorer prognosis, making it a tumor-associated antigen of interest for targeted therapeutics. Germline loss-of-function variants in ADAM9 are associated with inherited retinal dystrophies, underscoring physiological roles beyond cancer.