Recombinant Cynomolgus/Rhesus Macaque BCMA Fc Protein, CF Summary
Details of Functionality |
Measured by its ability to inhibit APRIL-mediated proliferation of anti-IgM stimulated mouse B cells. Moore, P.A. et al. (1999) Science 285:260; Gross, J.A. et al. (2000) Nature 404:995; Schneider, P. et al. (1999) J. Exp. Med. 189:1747. The ED50 for this effect is 30-180 ng/mL.
|
Source |
Human embryonic kidney cell, HEK293-derived BCMA/TNFRSF17 protein Cynomolgus Monkey BCMA (Met1-Ile54) Accession # XP_005591343 | IEGRMD | Human IgG1 (Pro100-Lys330) | N-terminus | | C-terminus | |
|
Accession # |
|
N-terminal Sequence |
Met1 |
Structure / Form |
Disulfide-linked homodimer |
Protein/Peptide Type |
Recombinant Proteins |
Purity |
>95%, 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 |
|
Theoretical MW |
33 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 |
37-43 kDa, reducing conditions |
Packaging, Storage & Formulations
Storage |
Use a manual defrost freezer and avoid repeated freeze-thaw cycles. - 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 with Trehalose. |
Purity |
>95%, 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 Cynomolgus/Rhesus Macaque BCMA Fc Protein, CF
Background
BCMA,
B cell maturation antigen, also known as Tumor Necrosis Factor Receptor Superfamily
member 17 (gene name TNSFR17), is a member of the TNFR superfamily, due to the
presence of its TNFR motif (1). BCMA is a type III membrane protein containing one extracellular cysteine rich domain, a
transmembrane domain, and an intracellular domain. Within the TNFRSF, it shares
the highest homology with TACI. BCMA and TACI have both been shown to bind to
APRIL and BAFF, members of the TNF ligand superfamily (2, 3). This
binding to APRIL and BAFF has been shown to stimulate IgM production in
peripheral B cells and increase the survival of cultured B cells (3, 4). This
data suggests that BCMA may play an important role in B cell development,
function and regulation (5). BCMA expression has been found in immune organs and
mature B cell lines (5). Although some expression has been observed at the cell
surface, BCMA appears to be localized to the Golgi compartment (6). Within the
ECD, cynomolgus monkey BCMA shares 89% sequence identity with human
BCMA, 62% with mouse BCMA, and 59% with rat BCMA.
The
expression of BCMA has also been linked to various cancers, autoimmune
disorders, and infectious diseases (7). Proteolytic shedding of the BCMA
extracellular domain generated soluble BCMA (sBCMA) via direct cleavage by gamma -secretase,
elevated sBCMA levels in serum may correlate with disease activity (8). More
recently, BCMA has been indicated as a possible biomarker in various human
immunological disease, and as a potential therapeutic target for multiple
myeloma (MM) (9-11).
- Hatzoglou, A. et al. (2000). J Immunol. 165:1322.
- Schiemann, B. et al. (2001). Science. 293:2111.
- Marsters, S.A. et al. (2000) Curr. Biol. 10:785.
- Huang, H. et al. (2013). PNAS. 110:10928.
- Laâbi, Y. et al. (1994). Nucleic Acids Res. 22:1147.
- Gras, M. et al. (1995) Int. Immunol. 7:1093.
- Coquery, C.M. et al. (2012) Crit Rev Immunol. 32:287.
- Laurent, S.A. et al. (2015) Nat Commun. 6:7333.
- Thaler, F.S. et al. (2017) Neuro Oncol. 19:1618.
- Seckinger, A. et al. (2017) Cancer Cell. 31:396.
- Lee, L. et al. (2018) Blood. 131:746.
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