>95%, by SDS-PAGE under reducing conditions and visualized by silver stain
Endotoxin Note
<0.01 EU per 1 μg of the protein by the LAL method.
Applications/Dilutions
Dilutions
Bioactivity
Theoretical MW
4.6 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
5 kDa, reducing conditions
Publications
Read Publication using 5987-BD in the following applications:
Use a manual defrost freezer and avoid repeated freeze-thaw cycles.
12 months from date of receipt, -20 to -70 °C as supplied.
1 month, 2 to 8 °C under sterile conditions after reconstitution.
3 months, -20 to -70 °C under sterile conditions after reconstitution.
Buffer
Lyophilized from a 0.2 μm filtered solution in HCl.
Purity
>95%, by SDS-PAGE under reducing conditions and visualized by silver stain
Reconstitution Instructions
Reconstitute at 500 μg/mL in 4 mM HCl.
Notes
This product is produced by and ships from R&D Systems, Inc., a Bio-Techne brand.
Alternate Names for Recombinant Mouse beta-Defensin 3 Protein, CF
BD14
BD3
BD-3
beta-defensin 103
betaDefensin 3
beta-Defensin 3
DEFB103
DEFB103A
DEFB103B
DEFB3
DEFB-3
DEFB3DEFB103A
Defensin, beta 103
defensin, beta 103B
Defensin-like protein
HBD-3
HBD3HBP3
Background
beta -defensin 3, also known as BD3 and DEFB-3, is a membrane-active cationic peptide that functions in inflammation and innate immune responses. There are at least 30 beta -defensins which are distinguished from alpha -defensins by the connectivity pattern of their three intramolecular disulfide bonds (1). The 41 aa mature mouse BD3 shares 38% and 59% aa sequence identity with human and rat BD3, respectively (2, 3). It shares 14% - 46% aa sequence identity with other mouse beta -defensins. BD3 is widely expressed among epithelial tissues, notably by keratinocytes and airway epithelial cells. It is up-regulated in response to proinflammatory cytokines, microbial and viral infections, and at the edges of skin wounds (2, 4 ‑ 6). BD3 induction in osteoarthritis chondrocytes promotes MMP1 and 13 production and inhibits TIMP1 and 2 expression (7). In vivo control of BD3 activity is accomplished in part through cleavage by cathepsins B, L, and S (8). BD3 displays strain specific microbicidal activity toward a broad spectrum of bacteria and yeast (2, 9). BD3 also induces monocyte migration, mast cell activation, and a mast cell-dependent increase in vascular permeability (4, 10). Disruption of the intramolecular disulfide bond pattern in BD3 abrogates its monocyte chemoattractant properties but not its antimicrobial properties (11, 12). BD3 inhibits viral infectivity by interacting directly with HIV-1 and its coreceptor CXCR4 (5, 13) and with HSV glycoprotein B and its receptor heparan sulfate (14), and by forming a protective coating on the surface of influenza virus target cells (15).
Dhople, V. et al. (2006) Biochim. Biophys. Acta. 1758:1499.
Bals, R. et al. (1999) Infect. Immun. 67:3542.
Schibli, D.J. et al. (2002) J. Biol. Chem. 277:8279.
Garcia, J.-R.C. et al. (2001) Cell Tissue Res. 306:257.
Quinones-Mateu, M.E. et al. (2003) AIDS 17:F39.
Sorensen, O.E. et al. (2006) J. Clin. Invest. 116:1878.
Varoga, D. et al. (2005) Arthritis Rheum. 52:1736.
Taggart, C.C. et al. (2003) J. Immunol. 171:931.
Joly, S. et al. (2004) J. Clin. Microbiol. 42:1024.
Chen, X. et al. (2007) Eur. J. Immunol. 37:434.
Kluver, E. et al. (2005) Biochemistry 44:9804.
Wu, Z. et al. (2003) Proc. Natl. Acad. Sci. 100:8880.
Beta-defensin-3: I may be small but I'm powerful! Beta-defensin 3 is a novel, non-hemolytic antimicrobial cationic peptide originally isolated from human lesional psoriatic scales and keratinocyte clones. It is a very small (2-6 kD) yet potent salt-insensitive broad spectrum antimicrobial that ta... Read full blog post.
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