CD112, His-Tag, Biotin-Labeled (Human) HiP™ Recombinant

Catalog #
71234
$435 *
Size: 50 µg
Qty
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Description

Human secreted CD112, encompassing amino acids 32-360. This construct has a C-terminal His-tag followed by an Avi-Tag™. This protein was enzymatically biotinylated using Avi-tag™ technology and was affinity purified. HiP™ indicates a high purity protein with ≥90% purity as measured by gel filtration.

Synonyms
Nectin-2, Herpes virus entry mediator B, HVEB, PVRL2, and PRR2
Product Info
Storage and Usage
Citations
Species
Human
Construct
CD112 (32-360-His-Avi)-(Biotin)
Host Species/Expression System
HEK293
Purity

≥90%

Format
Aqueous buffer solution
Formulation
8 mM phosphate, pH 7.4, 110 mM NaCl, 2.2 mM KCl, and 20% glycerol
MW
38 kDa + glycans
Amino Acids
32-360
Glycosylation
This protein runs at a higher MW by SDS-PAGE due to glycosylation.
Aggregation
<10%
Genbank #
NM_002856
UniProt #
Q92692
Tag(s)
C-terminal His-tag
Label

This protein is enzymatically biotinylated using Avi-Tag™ technology. Biotinylation confirmed to be ≥90%.

For more information on enzymatic biotinylation, please see our Tech Note.

Background

CD112 (Poliovirus receptor-related 2, PVRL2, or nectin-2), is widely expressed on antigen presenting cells and tumor cells and is the high affinity ligand of CD112R (Poliovirus receptor related immunoglobulin domain containing, PVRIG). CD112R is found in NK and T cells, and in T cells it is found particularly in CD8+ T cells. High levels of this protein are found in NK, CD8+ and CD4+ T cells of patients with kidney, ovary, lung, prostrate and endometrium cancer and acute myeloid leukemia (AML). CD112 has also been linked to tumor angiogenesis, growth and metastasis. It has a wider pattern of expression, being also present in endothelial cells, neurons and fibroblasts. CD112-CD112R interaction is a positive immune checkpoint that enhances human T cell response and has emerged as an attractive therapeutic target for oncology. TIGIT (T cell immunoreceptor with Ig and ITIM domains) and CD226 (also called DNAM-1, DNAX Accessory Molecule-1) also bind CD112. The development of inhibitors able to prevent the interaction between CD112R-CD112 alone or in combination with blockage of TIGIT-CD155/CD112 interaction may prove beneficial in cancer therapy.

References

1. Bottino, C., et al., J. Exp. Med. 2003; 198(4): 557-567.
2. Pende, D., et al., Blood. 2005; 105(5): 2066-2073.