GC Globulin [68476-36-8]
16-16-070307
Protein IDP02774
Product group Proteins / Signaling Molecules
Overview
- SupplierAthens Research
- Product NameGC Globulin [68476-36-8]
- Delivery Days Customer9
- Applications SupplierGlycobiology, Vitamin D Metabolism, Inflammation, Liver Damage/Disease, Itai-Itai Disease, Autoimmune Disease, Diabetes, In Vitro Diagnostic
- CertificationResearch Use Only
- Estimated Purity≥95% by SDS-PAGE
- Protein IDP02774
- Protein NameVitamin D-binding protein
- Scientific DescriptionVitamin D-binding protein (DBP/GC-globulin) serves as the primary transporter of vitamin D metabolites (25OHD, 1,25(OH)2D) in plasma, maintaining their solubility and bioavailability. Structurally, DBP comprises three domains, with domain I harboring a high-affinity binding site for vitamin D metabolites. Beyond sterol transport, DBP binds monomeric actin with nanomolar affinity, preventing pathological actin polymerization in circulation-a critical function during tissue injury. It also interacts with immune cells, binding to surface receptors on B and T lymphocytes to modulate chemotaxis and inflammatory responses. Reduced DBP levels correlate with severe liver diseases such as cirrhosis and acute-on-chronic liver failure, where impaired synthesis exacerbates vitamin D deficiency and actin scavenging dysfunction. In Itai-Itai disease, DBP loss in urine disrupts vitamin D transport, contributing to cadmium-induced osteomalacia7. Genetic polymorphisms (e.g., Gc1F, Gc1S, Gc2) influence DBP’s binding affinity, linking specific alleles to viral infection susceptibility and autoimmune disorders like lupus. Low DBP levels also associate with non-alcoholic fatty liver disease (NAFLD) progression and type 2 diabetes, where pancreatic alfa-cell dysfunction arises from disrupted actin cytoskeleton regulation.
- 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≤ -20° C
- UNSPSC41116100
References
- Chapron, B. D., et al., (2018), 'Reevaluating the Role of Megalin in Renal Vitamin D Homeostasis Using a Human Cell-Derived Microphysiological System', ALTEX 35(4): pp 504-515Read this paper
- Lidberg, K. A., et al., (2024), 'Modeling cellular responses to serum and vitamin D in microgravity using a human kidney microphysiological system', npj Microgravity 10: 75.Read this paper
- Gliozzi, M. L., et al., (2019), 'Hemoglobin alters vitamin carrier uptake and vitamin D metabolism in proximal tubule cells: implications for sickle cell disease', Am J Physiol Cell Physiol 317: pp C993–C1000Read this paper
- Kanie, Y., et al., (2023), 'Investigation of the Protective Effect for GcMAF by a Glycosidase Inhibitor and the Glycan Structure of Gc Protein', Molecules, 28: pp 1570.Read this paper
- Borges, C. R., et al., (2016), 'Glycan structure of Gc Protein-derived Macrophage Activating Factor as revealed by mass spectrometry', Archives of Biochemistry and Biophysics 606: pp 1e13Read this paper