Recombinant Mouse PIR-B Protein, CF Summary
Details of Functionality |
Measured by its binding ability in a functional ELISA. When biotinylated recombinant rat MAG/Siglec-4a Fc Chimera is catured on Streptavidin coated plate (Catalog # CP003) , Recombinant Mouse PIR-B binds with an apparent K d < 100 nM. |
Source |
Mouse myeloma cell line, NS0-derived mouse PIR-B protein Gly24-Gly635, with a C-terminal 6-His tag |
Accession # |
|
N-terminal Sequence |
Gly24 |
Protein/Peptide Type |
Recombinant Proteins |
Gene |
Pirb |
Purity |
>95%, by SDS-PAGE under reducing conditions and visualized by silver stain |
Endotoxin Note |
<0.10 EU per 1 μg of the protein by the LAL method. |
Applications/Dilutions
Dilutions |
|
Theoretical MW |
69 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 |
85-95 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 with trehalose |
Purity |
>95%, by SDS-PAGE under reducing conditions and visualized by silver stain |
Reconstitution Instructions |
Reconstitute at 250 μg/mL in sterile PBS. |
Notes
This product is produced by and ships from R&D Systems, Inc., a Bio-Techne brand.
Alternate Names for Recombinant Mouse PIR-B Protein, CF
Background
Paired immunoglobulin‑like receptor B (PIR‑B) is a transmembrane protein that acts as a negative regulator of immune responses. It is the rodent homolog of human LILRB1‑5 family proteins. It is most closely related to LILRB3 which is also known as ILT5, LIR‑3, and CD85a. Like LILRB family members, PIR‑B contains cytoplasmic immunoreceptor tyrosine‑based inhibitory motifs (ITIMs) that inhibit signaling events
via phosphatase SHP‑1. PIR‑A and other LILRA family members instead contain cytoplasmic ITAMs which augment immune responses (1). Mature mouse PIR‑B is a 120 kDa glycoprotein that consists of a 618 amino acid (aa) extracellular domain (ECD) with six Ig‑like domains, a 21 aa transmembrane segment, and a 178 aa cytoplasmic domain with four ITIMs (2). The 85‑95 kDa human ILT5 contains four Ig‑like domains. Within common regions of their ECDs, mouse PIR‑B shares 73% and 55% aa sequence identity with rat PIR‑B and human ILT5, respectively. PIR‑B is expressed on dendritic cells, monocytes, macrophages, B cells, mast cells, neutrophils, eosinophils, basophils, osteoclasts, and cerebellar granule neurons (3‑10). Triggering of PIR‑B inhibits the activation of macrophages, mast cells, neutrophils, basophils, and B cells (5‑7, 9). PIR‑B also inhibits the differentiation of osteoclasts and pro‑inflammatory M1 macrophages (4, 11). PIR‑B interacts
in cis and
in trans with MHC I molecules to limit autoreactive humoral and cellular immune responses (12‑14). It suppresses anti‑bacterial inflammatory responses by blocking TLR9‑dependent B cell activation (14). In the CNS, PIR‑B functions as a receptor for the myelin proteins Nogo, MAG, and OMgp and mediates their inhibitory action on neurite outgrowth and axon regeneration (10). Upon binding to MAG, PIR‑B associates with TrkB and NGF R/p75 in cerebellar granule neurons (15).
- Anderson, K.J. and R.L. Allen (2009) Immunology 127:8.
- Hayami, K. et al. (1997) J. Biol. Chem. 272:7320.
- Mitsuhashi, Y. et al. (2012) Blood 120:3256.
- Mori, Y. et al. (2008) J. Immunol. 181:4742.
- Pereira, S. et al. (2004) J. Immunol. 173:5757.
- Uehara, T. et al. (2001) J. Clin. Invest. 108:1041.
- Ujike, A. et al. (2002) Nat. Immunol. 3:542.
- Tedla, N. et al. (2003) Proc. Natl. Acad. Sci. USA 100:1174.
- Sloane, D.E. et al. (2004) Blood 104:2832.
- Atwal, J.K. et al. (2008) Science 322:967.
- Ma, G. et al. (2011) Immunity 34:385.
- Nakamura, A. et al. (2004) Nat. Immunol. 5:623.
- Endo, S. et al. (2008) Proc. Natl. Acad. Sci. USA 38:14515.
- Kubo, T. et al. (2009) J. Exp. Med. 206:1971.
- Fujita, Y. et al. (2011) Cell Death Dis. 2:e198.
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