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Recombinant Human PVRL2/Nectin-2/CD112 (C-mIgG2a Fc)

Uniprot : Q92692
  • Cat.No.:PKSH034051

  • Expression host: HEK293 Cells

To Purchase PKSH034051

Size:
  • 10μg
  • 50μg
Price: $104
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Description

Synonyms Poliovirus Receptor-Related Protein 2;Herpes Virus Entry Mediator B;Herpesvirus Entry Mediator B;HveB;Nectin-2;CD112;PVRL2;HVEB;PRR2
Species Human
Expression_host HEK293 Cells
Sequence Gln32-Leu360
Accession Q92692-2
Mol_Mass 62.6 kDa
AP_Mol_Mass 80-90 kDa
Tag C-mIgG2a Fc

Properties

Purity > 95 % as determined by reducing SDS-PAGE.
Endotoxin level < 1.0 EU per μg of the protein as determined by the LAL method.
Storage Generally, lyophilized proteins are stable for up to 12 months when stored at -20 to -80℃. Reconstituted protein solution can be stored at 4-8℃ for 2-7 days. Aliquots of reconstituted samples are stable at < -20℃ for 3 months.
Shipping This product is provided as lyophilized powder which is shipped with ice packs.
Formulation Lyophilized from a 0.2 μm filtered solution of PBS, pH 7.4.
Normally 5 % - 8 % trehalose, mannitol and 0.01% Tween80 are added as protectants before lyophilization.
Please refer to the specific buffer information in the printed manual.
Reconstitution Please refer to the printed manual for detailed information.

Background

CD112 is a type I transmembrane glycoprotein belonging to the Immunoglobulin superfamily. It comprises one Ig-like V-type domain and two Ig-like C2-type domains in the extracellular region. The V domain is believed to mediate nectin binding to its ligands. Nectin2 is known to bind the pseudorabies virus, and herpes simplex virus2 (HSV2), involving in cell to cell spreading of these viruses. It does not bind poliovirus. As a homophilic adhesion molecule, CD112 is found concentrated in adherens junctions, and exists on neurons, endothelial cells,epithelial cells and fibroblasts. CD112 has been identified as the ligand for DNAM-1 (CD226), and the interaction of CD226/CD112 mediates cytotoxicity and cytokine secretion by T and NK cells. The costimulatory responses may be a critical component in allergic reactions and may therefore become targets for anti-allergic therapy.

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