Recombinant Human LILRB4/CD85k/ILT3 Protein, CF Summary
Details of Functionality |
Measured by its binding ability in a functional ELISA. When Recombinant Human LILRB4/CD85k/ILT3 is coated at 2 μg/mL, Recombinant Human Angiopoietin-like Protein 7/ANGPTL7 (Catalog # 914-AN) binds with an apparent K d <1 nM. |
Source |
Mouse myeloma cell line, NS0-derived human LILRB4/CD85k/ILT3 protein Pro17-His257, with a C-terminal 6-His tag |
Accession # |
|
N-terminal Sequence |
Pro17& Ala (N+3 of signal derived sequence) |
Protein/Peptide Type |
Recombinant Proteins |
Gene |
LILRB4 |
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 |
27 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 |
29-43 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 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 PBS. |
Purity |
>95%, by SDS-PAGE visualized with Silver Staining and quantitative densitometry by Coomassie® Blue Staining. |
Reconstitution Instructions |
Reconstitute at 100 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 Human LILRB4/CD85k/ILT3 Protein, CF
Background
ILT3, also known as CD85k and LIR-5, is an approximately 60 kDa transmembrane glycoprotein that negatively regulates immune cell activation (1). Mature human ILT3 consists of a 238 amino acid (aa) extracellular domain with two Ig-like domains, a 21 aa transmembrane segment, and a 168 aa cytoplasmic domain with 3 immunoreceptor tyrosine-based inhibitory motifs (ITIM) (2). Alternative splicing of human ILT3 generates an isoform that lacks the first ITIM and a secreted isoform that circulates in the serum of cancer patients (3, 4). ILT3 is expressed on dendritic cells (DC), monocytes, macrophages, and vascular endothelial cells (EC) (2, 5, 6). Ligation of ILT3 triggers ITIM-mediated inhibition of cell-activating signaling, leading to enhanced immune tolerance and reduced allogeneic graft rejection (2, 4, 7, 8). Soluble ILT3 induces the differentiation of CD8
+ T suppressor cells (Ts) that can inhibit the effector functions of CD4
+ Th cells and CD8
+ CTL (4, 7, 9). In turn, CD8
+ Ts cells induce ILT3 up-regulation and a tolerogenic phenotype in monocytes, DC, and EC (5, 6, 8, 10, 11).
- Vlad, G. et al. (2010) Int. Rev. Immunol. 29:119.
- Cella, M. et al. (1997) J. Exp. Med. 185:1743.
- Heinzmann, A. et al. (2000) Eur. J. Immunogenet. 27:121.
- Suciu-Foca, N. et al. (2007) J. Immunol. 178:7432.
- Gleissner, C.A. et al. (2007) Eur. J. Immunol. 37:177.
- Manavalan, J.S. et al. (2004) Int. Immunol. 16:1055.
- Vlad, G. and N. Suciu-Foca (2012) Exp. Mol. Pathol. 93:294.
- Chang, C.C. et al. (2002) Nat. Immunol. 3:237.
- Vlad, G. et al. (2006) Int. Immunopharmacol. 6:1889.
- Manavalan, J.S. et al. (2003) Transpl. Immunol. 11:245.
- Brenk, M. et al. (2009) J. Immunol. 183:145.
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