When Recombinant Mouse BST-2/Tetherin (Catalog # 9940-BS) isimmobilized at 1 µg/mL (100 µL/well), Recombinant Viral Dengue Virus 4 EnvelopeFc Chimera binds with an ED50 of 0.2-1.6 μg/mL.
2 μg/lane of Recombinant Mouse BST-2/Tetherin (Catalog # 9940-BS) was resolved with SDS-PAGE under reducing (R) and non-reducing (NR) conditions and visualized by Coomassie® blue staining, showing bands at 13 kDa ...read more
Measured by its binding ability in a functional ELISA. When Recombinant Mouse BST-2/Tetherin (Catalog # 9940-BS) is immobilized at 1 µg/mL (100
µL/well), Recombinant Viral Dengue Virus 4 Envelope Fc Chimera binds with an ED50 of 0.2-1.6 μg/mL.
Source
E. coli-derived mouse BST-2/Tetherin protein Thr52-Ser152, with a C-Terminal 6-His tag
>90%, by SDS-PAGE visualized with Silver Staining and quantitative densitometry by Coomassie® Blue Staining.
Endotoxin Note
<0.10 EU per 1 μg of the protein by the LAL method.
Applications/Dilutions
Dilutions
Bioactivity
Theoretical MW
12 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
13 kDa and 28 kDa, reducing conditions
Publications
Read Publication using 9940-BS 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 MES and NaCl with Trehalose.
Purity
>90%, by SDS-PAGE visualized with Silver Staining and quantitative densitometry by Coomassie® Blue Staining.
Reconstitution Instructions
Reconstitute at 400 μg/mL in water.
Notes
This product is produced by and ships from R&D Systems, Inc., a Bio-Techne brand.
Alternate Names for Recombinant Mouse BST-2/Tetherin Protein, CF
bone marrow stromal antigen 2
bone marrow stromal cell antigen 2
BST2
BST-2
CD317 antigen
CD317
HM1.24 Antigen
NPC-A-7
PDCA-1
Tetherin
Background
BST-2, also known as tetherin or CD317, is a type II transmembrane
protein that is constitutively expressed in several cell types including T cells, B cells, monocytes and macrophages, as well as on several cancer cell
lines including the B cell lineage in multiple myeloma (1, 2). Originally named bone marrow stromal cell
antigen 2, BST-2 was identified to inhibit viral replication due to its unusual
topology (3-5). The extracellular
C-terminus of the protein is modified with GPI (glycosylphosphatidylinositol)
membrane anchor, which enables BST-2 to interact at each of its ends with the
cell or the viral membrane. The
ectodomain of the protein also contains three cysteine residues that can form
intermolecular disulfide bonds to form parallel dimers (2). Mouse BST-2 consists of a 30 amino acid (aa) cytoplasmic
domain, a 21 aa transmembrane segment, and a 101 aa extracellular domain
(ECD). Within the ECD, mouse BST-2
shares 41% and 71% aa sequence identity with human and rat BST-2, respectively.
BST-2 was identified as a major mediator of the innate immune defense against
enveloped viruses. BST-2 was shown to interact with formed viral particles tethering them to surface
of infected cells, thereby reducing viral release (6). BST-2 inhibits the release of diverse group of enveloped viruses including
members of the retrovirus, togavirus, filovirus, arenavirus, flavivirus,
rhabdovirus, orthohepadnavirus, orthomyxovirus, poxvirus, paramyxovirus, and
herpesvirus families (7-9). The mechanism BST-2 inhibition of viral budding was
suggested to be through directly bridging the host and viral membranes through
simultaneous embedding of its two opposing membrane anchors (9). To counteract
BST-2 functions, many viruses have evolved to develop strategies to antagonize
BST-2 function (9, 10). In addition to inhibiting viral release, BST-2 can act
as an innate immune sensor of viral infections by acting as a pattern
recognition receptor that activates NF-kappa B to induce inflammatory responses
through interactions with the immunoglobulin-like transcript 7 (ILT7/LILRA4)
(10, 11).
Evans, D.T. et al. (2010) Trens Microbiol. 18:388.
Ohtomo, T. et al. (1999) Biochem. Biophys. Res. Commun. 258:583.
Ishikawa, J. et al. (1995) Genomics. 26:527.
Neil, S.J. et al. (2008) Nature. 451:425.
Kupzig, S. et al. (2003) Traffic. 4:694.
Janvier K. et al. (2012) Curr HIV Res. 10:315.
Evans D.T. et al. (2010) Trends Microbiol. 18:388.
Mahauad-Fernandez W.D. et al. (2012) Immun Inflamm Dis. 4:4.
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