GC-Globulin, Human Plasma, Mixed Type (Vitamin D Binding Protein)

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1 mg
$75.00
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PRODUCT NUMBER:

16-16-070307

Buy Purified Native Human GC Globulin/Vitamin D Binding Protein direct from manufacturer.
Bulk Qty Available.

MW: 56,000
Extinction Coefficient: 0.63

Lyophilized from 20 mM Na phosphate, pH 7.4, with 150 mM NaCl.

Storage: -20°C

An alpha 2 glycoprotein composed of a single polypeptide chain and present in plasma at levels of 20-55 mg/100 ml. It functions in the binding and transport of vitamin D and may also play an important role in actin homeostatis since it has been shown to bind monomeric actin with high affinity. GC-globulin also binds membranes of both circulating B and T lymphocytes. Clinically, concentrations are reduced in patients with severe liver diseases. GC-globulin may also play an important role in the mechanism of the osteomalacia that occurs with Itai-Itai disease.

Purity: >=95% by SDS-PAGE

Prepared from plasma shown to be non reactive for HBsAg, anti-HCV, anti-HBc, and negative for anti-HIV 1 & 2 by FDA approved tests.

Athens Research & Technology products are laboratory reagents and are not to be administered to humans or used for any drug purpose. For research use only.

Product Citation:
Trujillo, Glenda, David M. Habiel, Lingyin Ge, Mahalakshmi Ramadass, Nancy E. Cooke, and Richard R. Kew. "Neutrophil Recruitment to the Lung in Both C5a-and CXCL1-Induced Alveolitis Is Impaired in Vitamin D–Binding Protein-Deficient Mice." The Journal of Immunology (2013).

Ge, Lingyin, Glenda Trujillo, Edmund J. Miller, and Richard R. Kew. "Circulating Complexes of the Vitamin D Binding Protein with G-Actin Induce Lung Inflammation by Targeting Endothelial Cells." Immunobiology (2013).

Kilpatrick LE.
Optimizing High Resolution Mass Spectrometry for the Identification of Low Abundance Post-Translational Modifications of Intact Proteins.
J Proteome Res. 2017 Aug 8. doi: 10.1021/acs.jproteome.7b00244. [Epub ahead of print].

Ramadass M, Ghebrehiwet B, Kew RR.
Enhanced recognition of plasma proteins in a non-native state by complement C3b. A possible clearance mechanism for damaged proteins in blood.
Mol Immunol. 2015 Mar;64(1):55-62. doi: 10.1016/j.molimm.2014.10.022. Epub 2014 Nov 15.

Ramadass M, Ghebrehiwet B, Smith RJ, Kew RR.
Generation of Multiple Fluid-Phase C3b:Plasma Protein Complexes during Complement Activation: Possible Implications in C3 Glomerulopathies.
J Immunol. 2014 Feb 1;192(3):1220-30. doi: 10.4049/jimmunol.1302288. Epub 2013 Dec 23.

Ref:
Lee, W.M. et al. 1987. Hepatology, 7, 825.
Teranishi, H. et al. 1983. Toxicol. Lett. 15, 7.