Recombinant Human KIR2DL3/CD158b2 Fc Chimera Protein, CF Summary
Details of Functionality
Measured by its ability to bind HEK293T human embryonic kidney cells in a flow cytometry assay. When 10 μg of Recombinant Human KIR2DL3/CD158b2 Fc Chimera is added to 5 x 105 HEK293T cells, >20% of the cells will bind to the protein.
Source
Mouse myeloma cell line, NS0-derived human KIR2DL3/CD158b2 protein
>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
51.2 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
66-75 kDa, reducing conditions
Publications
Read Publications using 2014-KR in the following applications:
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
>90%, by SDS-PAGE visualized with Silver Staining and quantitative densitometry by Coomassie® Blue Staining.
Reconstitution Instructions
Reconstitute at 500 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 KIR2DL3/CD158b2 Fc Chimera Protein, CF
CD158 antigen-like family member B2
CD158b2 antigen
CD158b2
CD158B2CD158b
cl-6
killer cell immunoglobulin-like receptor 2DL3
killer cell immunoglobulin-like receptor, two domains, long cytoplasmic tail, 3
Killer inhibitory receptor cl 2-3
KIR-023GB
KIR2DL3
KIRCL23
KIR-K7b
KIR-K7c
MGC129943
MHC class I NK cell receptor
natural killer associated transcript 2
natural killer cell inhibitory receptor KIR2DL3
Natural killer-associated transcript 2
NKAT
NKAT2
NKAT-2
NKAT2A
nkat2b
NKAT2GL183
NK-receptor
p58 natural killer cell receptor clone CL-6
p58 NK receptor CL-6
p58
p58.2 MHC class-I specific NK receptor
p58.2 MHC class-I-specific NK receptor
Background
KIR2DL3 (2DL3, formerly NKAT2, designated CD158b2) is a 341 amino acid (aa) type I transmembrane glycoprotein that belongs to the human killer cell Ig‑like receptor (KIR) family of molecules (1, 2). KIRs are expressed on human CD56dim NK cells and T cell subsets, and regulate effector functions in the innate immune system (1-3). KIRs are named for the number of Ig‑like domains (2D or 3D) in the extracellular domain (ECD), and whether they have long or short (L, S) cytoplasmic tails (1‑3). Individuals will express varying subsets of inhibiting and activating KIRs with varying polymorphisms (1, 4). Like other inhibiting KIRs, KIR2DL3 has two ITIM domains within its long tail that block activating receptor clustering (2). Within the ECD, KIR2DL3 shares very high aa sequence identity (98%) with KIR2DL2. The two segregate as alleles of the same gene; both recognize Asn80‑containing HLA‑C1 and, more weakly, Lys80‑containing C2 allotypes (1, 5). Extracellular aa identity is also high for KIR2DL1 (93%). The three molecules together recognize and inhibit NK cytotoxicity against cells expressing any HLA‑C allotype, allowing for self‑recognition (1‑3). Compared with KIR2DL2, KIR2DL3 shows lower avidity for HLA‑C1 ligands; when compared to KIR2DL1, KIR2DL3 has lower avidity but broader specificity for HLA-C1 ligands (1, 5, 6). Configurations of inhibiting and activating KIR can alter an individual’s susceptibility to viral and autoimmune diseases and leukemia (1‑3). For example, rheumatoid arthritis patients that are positive for KIR2DL3 and negative for KIR2DS3 have an earlier disease diagnosis (7).
Purdy, A.K. and Campbell, K.S. (2009) Cancer Biol. Ther. 8:13.
Lanier, L. L. (2005) Annu. Rev. Immunol. 23:225.
Kulkarni, S. et al. (2008) Semin. Immunol. 20:343.
Middleton, D. and F. Gonzelez (2009) Immunology 129:8.
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