This product is an unconjugated, non-therapeutic recombinant analog of tabalumab, built around the same molecular target (BAFF/TNFSF13B). It is supplied for research use only and is not the clinical drug, nor is it intended for human or veterinary use. The molecule reproduces the antigen-binding specificity of the originator (a human IgG4 framework carrying the S228P hinge stabilization) so that laboratories can study BAFF engagement, ligand neutralization, and antibody-format behavior in a controlled, reproducible reagent. Typical research applications include use as a defined binding and blocking tool, as a positive control or benchmarking standard in assay development, and as scaffold material for ADCC/ADC or engineering workflows. It is offered at low endotoxin (research grade less than 1 EU/mg; ultra-low grade less than 0.5 EU/mg) and in bulk milligram-to-gram quantities to support in-vitro assays, screening, and preclinical model work. Because it is manufactured as a research analog rather than a licensed therapeutic, it provides a cost-effective, consistent source of a well-characterized anti-BAFF reagent for method comparison and target-biology studies.
BAFF (B-cell activating factor; also BLyS, TALL-1, TNFSF13B; UniProt Q9Y275) is a type II transmembrane cytokine of the TNF superfamily, expressed largely by myeloid cells, dendritic cells, and stromal cells. It is cleaved from the surface to release a soluble form that assembles into trimers and higher-order 60-mer structures. BAFF signals through three receptors on B lineage cells: BAFF-R (TNFRSF13C), TACI (TNFRSF13B), and BCMA (TNFRSF17). Engagement, chiefly via BAFF-R, delivers survival and maturation signals to transitional and mature B cells, supporting peripheral B-cell homeostasis, selection, and immunoglobulin production. BAFF shares the receptors TACI and BCMA with the related ligand APRIL. Excess BAFF availability promotes survival of autoreactive B cells, and elevated BAFF is associated with systemic lupus erythematosus and other autoimmune conditions, making the ligand a validated target for B-cell-directed intervention.