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Recombinant Human Vitamin D BP His-tag Protein, CF

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2 μg/lane of Recombinant Vitamin D BP was resolved with SDS-PAGE underreducing (R) and non-reducing (NR) conditions and visualized by Coomassie® Bluestaining, showing bands at 57-63 kDa and 45-50 kDa, respectively.

Product Details

Summary
Reactivity HuSpecies Glossary
Applications Bioactivity
Format
Carrier-Free

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Recombinant Human Vitamin D BP His-tag Protein, CF Summary

Details of Functionality
Measured by its binding ability in a functional ELISA. When Vitamin D3-BSA Conjugate is immobilized at 2 μg/mL, 100 μL/well, Recombinant Human Vitamin D BP binds with an ED50 of 2‑10 μg/mL.
Source
Mouse myeloma cell line, NS0-derived human Vitamin D BP protein
Leu17-Leu474 (K436T), with a C-terminal 6-His tag
Accession #
N-terminal Sequence
Leu17
Protein/Peptide Type
Recombinant Proteins
Purity
>90%, by SDS-PAGE visualized with Silver Staining and quantitative densitometry by Coomassie® Blue Staining.
Purity Statement
Antigen Affinity-purified
Endotoxin Note
<0.10 EU per 1 μg of the protein by the LAL method.

Applications/Dilutions

Dilutions
  • Bioactivity
Theoretical MW
52 kDa.
Disclaimer note: The observed molecular weight of the protein may vary from the listed predicted molecular weight due to post translational modifications, post translation cleavages, relative charges, and other experimental factors.
SDS-PAGE
57-63 kDa, reducing conditions

Packaging, Storage & Formulations

Storage
  • 12 months from date of receipt, ≤ -20 °C as supplied.
  • 1 month, 2 to 8 °C under sterile conditions after reconstitution.
  • 3 months, ≤ -20 °C under sterile conditions after reconstitution.
Buffer
Lyophilized from a 0.2 μm filtered solution in PBS.
Purity
>90%, by SDS-PAGE visualized with Silver Staining and quantitative densitometry by Coomassie® Blue Staining.
Reconstitution Instructions
Reconstitute at 500 μg/mL in PBS.

Notes

This product is produced by and ships from R&D Systems, Inc., a Bio-Techne brand.

Alternate Names for Recombinant Human Vitamin D BP His-tag Protein, CF

  • DBP
  • DBP/GC
  • DBP-MAF
  • DBPVDBG
  • EC 6.3.1.5
  • Gc
  • gc-globulin
  • Gc-MAF
  • GRD3
  • group-specific component (vitamin D binding protein)
  • Group-specific component
  • hDBP
  • VDB
  • VDBG
  • VDBP
  • Vitamin D BP
  • vitamin D-binding alpha-globulin
  • vitamin D-binding protein

Background

Vitamin D BP (Vitamin D binding protein), also known as group-specific component and GC-globulin, is a 58 kDa, monomeric glycoprotein member of the ALB/AFP/VDB family. It was initially discovered as a major liver-derived polymorphic protein and was called group-specific component or GC in 1959 (1). Mature human Vitamin D BP is 458 amino acids (aa) in length. It contains three albumin-type domains that are accompanied by 14 intramolecular disulfide bonds (2). Mature human Vitamin D BP  is 77% aa identical to mouse Vitamin D BP. Vitamin D BP is able to bind to various forms of Vitamin D including vitamin D2, the 25‑hydroxylated forms and the active hormonal product, 1,25-dihydroxyvitamin D (Calcitriol). The major proportion of Vitamin D in blood is bound to Vitamin D BP, which transports vitamin D metabolites between skin, liver and kidney and then on to various target tissues (3). Vitamin D BP is implemented as a cause for multiple sclerosis (4). There is a strong suggestion that vitamin D and Vitamin D BP  gene polymorphism are involved in occurrence of type 2 diabetes mellitus (5). Vitamin D BP  has been associated with inflammatory process, stimulation of chemotaxis by phagocytic neutrophils and the activation and stimulation of phagocytic function by macrophages (6, 7).
  1. Hirschfeld, J. (1959) Acta. Pathol. Microbiol. Scand. 47:160.
  2. Schoentgen, F. et al. (1986) Biochim. Biophys. Acta. 871:189.
  3. Verboven, C. et al. (2002) Nat. Struct. Biol. 9:131.
  4. Langer-Gould, A. et al. (2018) Nutrients. 10:E184.
  5. Rahman, M.M. et al. (2017) Gene 636:42.
  6. Binder, R. et al. (1999) Mol. Immunol. 36:885.
  7. Kew, R.R. et al. (1995) J Immunol. 155:5369.

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