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HRP-2275 Recombinant Human CD155 Protein $200
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Recombinant Human CD155 Protein

Product Name: Recombinant Human CD155 Protein
Catalog #:  HRP-2275
Manufacture:  LD Biopharma, Inc.
Intruduction:

Human CD155 gene encodes a trans-membrane protein which mediates NK cell adhesion and triggers NK cell effector functions. It binds two different NK cell receptors: CD96 and CD226. These interactions accumulate at the cell-cell contact site, leading to the formation of a mature immunological synapse between NK cell and target cell. This may trigger adhesion and secretion of lytic granules and IFN-gamma and activate cytoxicity of activated NK cells. CD155 may also promote NK cell-target cell modular exchange, and PVR transfer to the NK cell. This transfer is more important in some tumor cells expressing a lot of PVR, and may trigger fratricide NK cell activation, providing tumors with a mechanism of immune-evasion. CD155 plays a role in mediating tumor cell invasion and migration. CD155 serves as a receptor for poliovirus attachment to target cells. It may play a role in axonal transport of poliovirus, by targeting virion-PVR-containing endocytic vesicles to the microtubular network through interaction with DYNLT1. This interaction would drive the virus-containing vesicle to the axonal retrograde transport. CD155 can form trans-heterodimers with PVRL3/nectin-3. The extracellular domain interacts with VTN, CD226 and CD96. The cytoplasmic domain interacts with DYNLT1. Interacts with HHV-5 UL141. Interacts with poliovirus capsid composed of VP1, VP2 and VP3, mainly through VP3. It also binds with high affinity to TIGIT.

Full-length extracellular domain of human CD155 cDNA (21 – 343aa, derived from BC015542) was constructed with codon optimization gene synthesis and expressed with a human alpha Fetal Protein N-terminal (AFPn) -His-TEV cleavage site Tag (217aa) fusion at its N-terminall. This protein was expressed in E. coli as inclusion bodies. The final product was refolded using our unique “temperature shift inclusion body refolding” technology and chromatographically purified.

Gene Symbol:  CD155 (PVR; HVED; Necl-5; PVS; TAGE4) 
Accession Number:  NP_006496
Species:  Human
Package Size:  20 µg / Vial   
Composition: 0.2 mg/ml, sterile-filtered, in 20 mM pH 8.0 Tris-HCl Buffer, with proprietary formulation of NaCl, KCl, EDTA, Sucrose and DTT.
Storage: In Liquid. Keep at -80°C for long term storage. Product is stable at 4 °C for at least 30 days.
Key Reference: Gao J, et al., CD155, an onco-immunologic molecule in human tumors Cancer Sci. 108 (10), 1934-1938 (2017)
Takahashi N, et al., Increased Soluble CD226 in Sera of Patients with Cutaneous T-Cell Lymphoma Mediates Cytotoxic Activity against Tumor Cells via CD155. J. Invest. Dermatol. 137 (8), 1766-1773 (2017)
Pignoloni B, et al., Distinct Roles for Human Cytomegalovirus Immediate Early Proteins IE1 and IE2 in the Transcriptional Regulation of MICA and PVR/CD155 Expression. J. Immunol. 197 (10), 4066-4078 (2016)
Iguchi-Manaka A, et al., Increased Soluble CD155 in the Serum of Cancer Patients. PLoS ONE 11 (4), E0152982 (2016)
Applications:

1. May be used for in vitro CD155 mediated NK activation regulation study with this protein either as soluble factor or as coating matrix protein.

2. May be used for protein-protein interaction assay.

3. Potential Therapeutic, which may be used as NK activities regulator for immune-modulating in vivo (recombinant CD155 protein or anti-CD155 antibody) for various diseases.

Quality Control: Purity: > 90% by SDS-PAGE.
Recombinant Protein Sequence: MTLHRNEYGIASILDSYQCTAEISLADLATIFFAQFVQEATYKEVSKMVKDALTAIEKPTGDEQSSGCLENQLPAFLEELCHEKEILEKYGHSDCCSQSEEGRHNCFLAHKKPTPASIPLFQVPEPVTSCEAYEEDRETFMNKFIYEIARRHPFLYAPTILLWAARYDKIIPSCCKAENAVECFQTKAATVTKELRESSGGSHHHHHHGSENLYFQGWPPPGTGDVVVQAPTQVPGFLGDSVTLPCYLQVPNMEVTHVSQLTWARHGESGSMAVFHQTQGPSYSESKRLEFVAARLGAELRNASLRMFGLRVEDEGNYTCLFVTFPQGSRSVDIWLRVLAKPQNTAEVQKVQLTGEPVPMARCVSTGGRPPAQITWHSDLGGMPNTSQVPGFLSGTVTVTSLWILVPSSQVDGKNVTCKVEHESFEKPQLLTVNLTVYYPPEVSISGYDNNWYLGQNEATLTCDARSNPEPTGYNWSTTMGPLPPFAVAQGAQLLIRPVDKPINTTLICNVTNALGARQAELTVQVKEGPPSEHSGISRN
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