Immunoglobulin G Fab Fragment
16-16-090707-Fab
Product group Proteins / Signaling Molecules
Overview
- SupplierAthens Research
- Product NameImmunoglobulin G Fab Fragment
- Delivery Days Customer9
- Applications SupplierBiotherapeutics, Flow Cytometry, Immunohistochemistry, Antisera Production
- CertificationResearch Use Only
- Estimated Purity≥95% by SDS-PAGE. No reaction by IEP to antisera to human IgG-fc.
- Scientific DescriptionThe IgG Fab (Fragment antigen-binding) fragment is a monovalent proteolytic product of Immunoglobulin G. Each Fab fragment retains the variable domains (VH and VL) responsible for antigen specificity while lacking the Fc-mediated effector functions, enabling targeted antigen neutralization without immune activation. This structural configuration prevents cross-linking-induced precipitation or cellular patching/capping, making Fab fragments ideal for precise antigen targeting in solution or on cell surfaces. Diagnostically, Fab fragments enable multiplex immunoassays by preventing Fc-mediated cross-reactivity, facilitating simultaneous detection of multiple antigens in flow cytometry and immunohistochemistry. Their monovalent nature ensures minimal background noise in assays requiring high specificity. Emerging applications include autoimmune disease management, where Fab fragments neutralize autoantibodies while circumventing complement activation. By combining targeted binding with reduced immunogenicity, IgG Fab fragments represent a versatile tool in both clinical and research settings.
- Shelf life instructionmore then 1 year
- SourceSource human plasma non-reactive for HBsAG, anti-HCV, anti-HBc, and negative for anti-HIV 1 & 2 by FDA approved tests.
- Storage Instruction-20C
- UNSPSC41116100
References
- Padmanabhan, A., et al., (2017), 'IVIg for Treatment of Severe Refractory Heparin-Induced Thrombocytopenia', CHEST, 152(3): pp 478-485.Read this paper
- Fletcher, N. A., et al., (2016), 'Controlled delivery of antibodies from injectable hydrogels', Materials Science and Engineering C 59: pp 801–806.Read this paper
- Karau, M. J., et al., (2017), 'Passive therapy with humanized antistaphylococcal enterotoxin B antibodies attenuates systemic inflammatory response and protects from lethal pneumonia caused by staphylococcal enterotoxin B-producing Staphylococcus aureus', VIRULENCE. 8(7): pp 1148–1159Read this paper
- Kilgore, R., et al., (2023), 'Development of peptide affinity ligands for the purification of polyclonal and monoclonal Fabs from recombinant fluids', Journal of Chromatography A 1687: pp 463701Read this paper
- Ngatuni, M. J., et al., (2018), 'Novel Random Triblock Copolymers for Sustained Delivery of Macromolecules for the Treatment of Ocular Diseases', AAPS PharmSciTech, 19(8): pp 3871-3885Read this paper