Recombinant Human LILRB1/CD85j/ILT2 Fc Chimera (Catalog #2017-T2) supports the adhesion of HSB2 humanperipheral blood acute lymphoblastic leukemia cells. Immobilized RecombinantHuman LILRB1/CD85j/ILT2 Fc Chimera at 5 ...read more
Recombinant Human LILRB1/CD85j/ILT2 Fc Chimera Protein, CF Summary
Details of Functionality
Measured by its ability to support the adhesion of HSB2 human peripheral blood acute lymphoblastic leukemia cells. Immobilized Recombinant Human LILRB1/CD85j/ILT2 Fc Chimera at 5 µg/mL, 100 µL/well can support 60-80% HSB2 cell adhesion, when 1 x 105 cells were added in each well of a 96-well plate.
Source
Mouse myeloma cell line, NS0-derived human LILRB1/CD85j/ILT2 protein
Human LILRB1/CD85j/ILT2 (Gly24-His458) Accession # Q8NHL6
>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
73.8 kDa (monomer). 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
106 kDa, reducing conditions
Publications
Read Publications using 2017-T2 in the following applications:
LILRB1, also known as CD85j and ILT2, is a 110 kDa transmembrane glycoprotein in the LILR immunoregulatory protein family (1). Mature human LILRB1 consists of a 438 amino acid (aa) extracellular domain (ECD) with 4 tandem Ig-like domains, a 21 aa transmembrane segment, and a 168 aa cytoplasmic domain with 4 inhibitory ITIM motifs (2). Alternative splicing generates an additional isoform that lacks the transmembrane and cytoplasmic regions (3). LILRB1 is expressed on the surface of B cells and monocytes, as well as subsets of NK cells, memory/effector CD8+ T cells, gamma δ T cells, and monocyte-derived dendritic cells (3-7). LILRB1 binds to MHC-I as well as non-classical MHC-I molecules (e.g. HLA-F, HLA-G, and HC-B27) and the MHC-I mimetic UL18 encoded by cytomegalovirus (3, 5, 8-10). R&D Systems in-house testing indicates that LILRB1 also binds to Angiopoietin-like 7. Ligation of LILRB1 inhibits the antigen induced proliferation and activation of CD8+ T cells, CD4+ T cells, NK cells, and gamma δ T cells (3, 4, 11-13). On dendritic cells, ligation inhibits the production of IL-10, IL-12p70, and TGF-beta and protects from Fas-mediated apoptosis (7).
Thomas, R. et al. (2010) Clin. Rev. Allergy Immunol. 38:159.
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Colonna, M. et al. (1997) J. Exp. Med. 186:1809.
Harly, C. et al. (2011) Blood 117:2864.
Cosman, D. et al. (1997) Immunity 7:273.
Young, N.T. et al. (2001) J. Immunol. 166:3933.
Young, N.T. et al. (2008) Blood 111:3090.
Lepin, E.J.M. et al. (2000) Eur. J. Immunol. 30:3552.
Shiroishi, M. et al. (2003) Proc. Natl. Acad. Sci. USA 100:8856.
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