Mouse BAFF/BLyS/TNFSF13B Antibody Summary
Ala127-Leu309
Accession # Q9WU72
Applications
Please Note: Optimal dilutions should be determined by each laboratory for each application. General Protocols are available in the Technical Information section on our website.
Scientific Data
![Cell Proliferation Induced by BAFF/BLyS/TNFSF13B and Neutralization by Mouse BAFF/BLyS/TNFSF13B Antibody. Cell Proliferation Induced by BAFF/BLyS/TNFSF13B and Neutralization by Mouse BAFF/BLyS/TNFSF13B Antibody.](https://resources.rndsystems.com/images/datasheets/antibody/BAFF_AF2106_Block_Neutralize_8815.jpg)
Cell Proliferation Induced by BAFF/BLyS/TNFSF13B and Neutralization by Mouse BAFF/BLyS/TNFSF13B Antibody. In the presence of Goat F(ab')2 Anti-mouse IgM, Recombinant Mouse BAFF/BLyS/ TNFSF13B (Catalog # 8876-BF) stimulates pro-liferation in mouse B cells in a dose-dependent manner (orange line). Under these conditions, proliferation elicited by Recombinant Goat Anti-Mouse BAFF/BLyS/TNFSF13B (3 ng/mL) is neutralized (green line) by increasing concentrations of Mouse BAFF/BLyS/TNFSF13B Antigen Affinity-purified Polyclonal Antibody (Catalog # AF2106). The ND50 is typically 0.01-0.04 µg/mL.
Reconstitution Calculator
Preparation and Storage
- 12 months from date of receipt, -20 to -70 °C as supplied.
- 1 month, 2 to 8 °C under sterile conditions after reconstitution.
- 6 months, -20 to -70 °C under sterile conditions after reconstitution.
Background: BAFF/BLyS/TNFSF13B
BAFF (also known as TALL-1, BLyS, THANK) is a type II transmembrane glycoprotein belonging to the TNF superfamily and has been designated as TNF superfamily member 13B (TNFSF13B). Mouse BAFF is a 309 aa protein consisting of a 248 amino acid (aa) extracellular domain, a 21 aa transmembrane region and a 45 aa cytoplasmic tail (1, 2). BAFF has the typical structural characteristics of the TNF superfamily ligands. It is a homotrimeric protein having the structurally conserved motif known as TNF homology domain (3, 4). A higher ordered structure composed of a cluster of trimeric units resembling the structure of a viral capsid has also been reported (4). Mouse BAFF may be shed from the cell surface by proteolytic cleavage between R126 and Ala 127 to yield a soluble form of the protein detectable in serum (1, 5). Within the TNF superfamily BAFF shares the highest homology (48%) with APRIL (1). BAFF shares with APRIL the ability to bind to BCMA and TACI and also binds specifically to BAFF receptor (BAFF R, also known as BR3 or TNFSFR13C), which is the principal BAFF receptor (6-8). All three receptors are type III transmembrane proteins that are expressed in B cells. BAFF and APRIL can form active heteromers that bind TACI (9). BAFF is expressed in peripheral blood mononuclear cells, in spleen and lymph nodes. Its expression in resting monocytes is upregulated by IFN-alpha, IFN-beta, LPS and IL-10. BAFF provides critical survival signals to a subset of B cells with intermediate maturation status (T2 B cells) during the immune response (10). BAFF also plays an important role in the development of lymphoid tissue and enhances the survival of activated memory B cells (7, 11). Human and mouse BAFF share 86% aa sequence identity (1).
- Schneider, P. et al. (1999) J. Exp. Med. 189:1747.
- Mukhopadhyay, A. et al. (1999) J. Biol. Chem. 274:15978.
- Karpusas, M. et al. (2002) J. Mol. Biol. 315:1145.
- Liu, Y. et al. (2002) Cell 108:383.
- Cheema, G.S. et al. (2001) Arthr. Rheum. 44:1313.
- Marsters, S.A. et al. (2000) Curr. Biol. 10:785.
- Thompson, J.S. et al. (2001) Science 293:2108.
- Ng, L. G. et al. (2004) J. Immunol. 173:807.
- Roschke, V. et al. (2002) J. Immunol. 169:4314.
- Batten, M. et al. (2000) J. Exp. Med. 192:1453.
- Avery, D.T. et al. (2003) J. Clin. Invest. 112:286.
Product Datasheets
Citations for Mouse BAFF/BLyS/TNFSF13B Antibody
R&D Systems personnel manually curate a database that contains references using R&D Systems products. The data collected includes not only links to publications in PubMed, but also provides information about sample types, species, and experimental conditions.
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Citations: Showing 1 - 8
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BAFF-secreting neutrophils drive plasma cell responses during emergency granulopoiesis
J Exp Med, 2016-07-18;0(0):.
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Venous-plexus-associated lymphoid hubs support meningeal humoral immunity
Authors: Fitzpatrick, Z;Ghabdan Zanluqui, N;Rosenblum, JS;Tuong, ZK;Lee, CYC;Chandrashekhar, V;Negro-Demontel, ML;Stewart, AP;Posner, DA;Buckley, M;Allinson, KSJ;Mastorakos, P;Chittiboina, P;Maric, D;Donahue, D;Helmy, A;Tajsic, T;Ferdinand, JR;Portet, A;Peñalver, A;Gillman, E;Zhuang, Z;Clatworthy, MR;McGavern, DB;
Nature
Species: Mouse
Sample Types: Whole Tissue
Applications: Immunohistochemistry -
Neutrophils license iNKT cells to regulate self-reactive mouse B cell responses
Nat. Immunol., 2016-10-31;0(0):.
Species: Mouse
Sample Types: Whole Cells
Applications: Neutralization -
The BAFF receptor TACI controls IL-10 production by regulatory B cells and CLL B cells.
Authors: Saulep-Easton D, Vincent F, Quah P, Wei A, Ting S, Croce C, Tam C, Mackay F
Leukemia, 2015-07-03;30(1):163-72.
Species: Mouse
Sample Types: Whole Cells
Applications: Neutralization -
Functional implication of BAFF synthesis and release in gangliosides-stimulated microglia.
Authors: Kim KS, Park JY, Jou I, Park SM
J. Leukoc. Biol., 2009-04-30;86(2):349-59.
Species: Mouse
Sample Types: Whole Cells
Applications: Flow Cytometry -
An Inflammatory Loop Between Spleen-Derived Myeloid Cells and CD4+ T Cells Leads to Accumulation of Long-Lived Plasma Cells That Exacerbates Lupus Autoimmunity
Authors: Eunkyeong Jang, Somi Cho, Sungjin Pyo, Jin-Wu Nam, Jeehee Youn
Frontiers in Immunology
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Incorporating B cell activating factor (BAFF) into the membrane of rabies virus (RABV) particles improves the speed and magnitude of vaccine-induced antibody responses
Authors: Joseph R. Plummer, James P. McGettigan
PLOS Neglected Tropical Diseases
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Neutrophils drive type I interferon production and autoantibodies in patients with Wiskott-Aldrich syndrome
Authors: Karla E. Cervantes-Luevano, Nicoletta Caronni, Maria C. Castiello, Elena Fontana, Giulia M. Piperno, Asma Naseem et al.
Journal of Allergy and Clinical Immunology
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