Human LILRB1 / CD85j / ILT2 Protein, Fc Tag
Proteins and Peptides
- 貨號 Cat. No.
- CDJ-H5252
- 規格 Size
- 100ug
- 品牌 Brand
- ACROBiosystems
- Species
- Human
- Conjugate
- Unconjugated
- Expression System
- HEK293
- Tag
- Fc Tag
Description
Source :
Human LILRB1, Fc Tag (CDJ-H5252) is expressed from human 293 cells (HEK293). It contains AA Gly 24 - His 458 (Accession # D9IDM8-1).
Molecule : LILRB1
Synonyms : CD85J,LILRB1,CD85,ILT2,LIR1,MIR7
Format : Powder
Category : Immune Checkpoint Proteins
Accession : AAH15731.1
Storage : -20℃
Shipping condition : Powder,RT
Molecular Weight : 73.8 kDa
Characteristics :
This protein carries a human IgG1 Fc tag at the C-terminus. The protein has a calculated MW of 73.8 kDa. The protein migrates as 90-105 kDa under reducing (R) condition (SDS-PAGE) due to glycosylation.
Endotoxin Level : Less than 1.0 EU per μg by the LAL method.
Buffer : 50 mM Tris, 100 mM Glycine, pH7.5
Description :
CD85 antigen-like family member J (CD85J) is also known as Leukocyte immunoglobulin-like receptor subfamily B member 1 (LILRB1 or LIR-1), Immunoglobulin-like transcript 2 (ILT-2), Monocyte/macrophage immunoglobulin-like receptor 7 (MIR7), which belongs to leukocyte immunoglobulin-like receptor (LIR) family. CD85J / LILRB1 Contains 4 Ig-like C2-type (immunoglobulin-like) domains. CD85J / LIR-1 is expressed predominantly on B-cells and monocytes. CD85J is receptor for class I MHC antigens and recognizes a broad spectrum of HLA-A, HLA-B, HLA-C and HLA-G alleles and is also receptor for H301/UL18, a human cytomegalovirus class I MHC homolog. Ligand binding results in inhibitory signals and down-regulation of the immune response. CD85J / LILRB1 interaction with HLA-B or HLA-E leads to inhibition of the signal triggered by FCER1A and inhibits serotonin release. CD85J / LILRB1 inhibits FCGR1A-mediated phosphorylation of cellular proteins and mobilization of intracellular calcium ions.
References :
(1) Cosman D., et al., 1997, Immunity 7:273-282.
(2) Fanger N.A., et al., 1998, Eur. J. Immunol. 28:3423-3434.
(3) Chapman T.L., et al., 1999, Immunity 11:603-613.
(4) Bellon T., et al., 2002, J. Immunol. 168:3351-3359.

