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Brand: ProteoGenix

Nipah virus(HeV) -Fusion glycoprotein F0 recombinant protein

Host species:
Mammalian cells
Origin species:
Nipah virus(HeV)
Uniprot ID:
Q9IH63
Molecular weight:
57.71 kDa

420.00

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Ile27–Ser493 His
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Nipah virus(HeV) -Fusion glycoprotein F0 recombinant protein

Product name Nipah virus(HeV) -Fusion glycoprotein F0 recombinant protein
Uniprot ID Q9IH63
Origin species Nipah virus(HeV)
Expression system Eukaryotic expression
Molecular weight 57.71 kDa
Protein delivered with Tag? C-Terminal His Tag
Purity estimated >85% by SDS-PAGE
Buffer Lyophilized from a solution in PBS pH 7.4, 1mM EDTA, 4% Trehalose, 1% Mannitol.
Delivery condition Dry Ice
Delivery lead time in business days 3-5 days if in stock; 3-5 weeks if production needed
Storage condition 4°C for short term (1 week), -20°C or -80°C for long term (avoid freezing/thawing cycles; addition of 20-40% glycerol improves cryoprotection)
Brand ProteoGenix
Host species Mammalian cells
Fragment Type Ile27-Ser493
Aliases /Synonyms Fusion glycoprotein F0, Protein F, Fusion glycoprotein F2, Fusion glycoprotein F1, F, Nipah Virus (NiV) / Hendra Virus (HeV)
Reference PX-P6240
Note For research use only.
Molecular Constructor
Ile27–Ser493 His

Nipah Virus (HeV) Structure

Nipah virus (HeV) is a negative-sense, single-stranded RNA virus belonging to the family Paramyxoviridae. It is composed of a nucleocapsid core surrounded by a lipid envelope and a matrix protein. Its genome is 15,000 nucleotides in length, and it encodes six structural proteins and four non-structural proteins.

Nipah Virus (HeV) Activity

The activity of the Nipah virus (HeV) is mediated by its structural proteins. The F and G glycoproteins form the virus’ fusion complex, allowing it to enter host cells and fuse with the host cell membrane. The matrix protein M is involved in viral assembly and budding from the host cell. The nucleocapsid protein N is involved in the formation of the viral ribonucleoprotein complex.

Nipah Virus (HeV) Drug Target

The F fusion glycoprotein F0 is a potential drug target for Nipah virus (HeV). This protein is essential for the virus’ entry into host cells and is a promising target for vaccine and therapeutic strategies. Inhibition of the F0 glycoprotein could prevent the virus from entering host cells, thus preventing infection.

  • Bezeljak U, Jerman A, Kobal T, et al. Purification and immunogenicity of Nipah virus-like particles from insect cells. BMC Biotechnology. 2025 Dec;26(1):14. DOI: 10.1186/s12896-025-01095-w. PMID: 41476213; PMCID: PMC12866483 https://doi.org/10.1186/s12896-025-01095-w
  • Stewart, M., Bone, P., Bacon, A. et al. Protective immunity in hamsters from an oral Nipah vaccine correlates with pseudovirus neutralising antibody titre. Sci Rep (2026).https://doi.org/10.1038/s41598-026-40205-2

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