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홈 > Research Area > 박테리아 및 바이러스 관련 제품 > Lujo virus (LUJV)

Lujo Virus (LUJV) Research Reagents — Antibodies & Recombinant Proteins

Lujo virus (LUJV) is an enveloped, bi-segmented, ambisense RNA mammarenavirus first identified during a 2008 nosocomial outbreak in Johannesburg, South Africa, with an 80% case fatality rate (4 of 5 confirmed cases died) — one of the highest mortality rates ever recorded for an arenavirus. LUJV is phylogenetically unique: it is the only known Old World arenavirus that uses neuropilin-2 (NRP2) as its entry receptor, rather than α-dystroglycan used by LASV and LCMV. This distinct receptor usage, combined with its extreme virulence and potential for nosocomial transmission, makes LUJV a high-priority pathogen for pre-pandemic preparedness. The genome encodes four proteins: GP1 (receptor binding via NRP2), GP2 (class I fusion), Z protein (RING-domain matrix, drives budding), and NP (nucleoprotein, though NP products are not yet available in this panel).

Research Use OnlyNot for diagnostic or therapeutic use.

abinScience is one of the few suppliers worldwide offering dedicated Lujo virus reagents — covering GP1 (receptor-binding subunit, three tag formats), GP2 (fusion subunit), and Z protein (matrix) — with polyclonal detection antibodies. All products are recombinant — no BSL-4 required. Manufactured by AtaGenix Laboratories (ISO 9001 & ISO 13485). Contact us for custom NP development and bulk orders.

Key Research Targets

Glycoprotein GP1 — NRP2 Receptor Binding
GP1 mediates viral attachment via neuropilin-2 (NRP2) — a unique receptor usage among arenaviruses that distinguishes LUJV from all other known Old World arenaviruses. GP1 is the primary target for neutralizing antibodies and the key antigen for understanding LUJV cell tropism and zoonotic potential. Available in three tag formats for maximum assay flexibility:
• GP1 C-Fc (VK092011) — Fc-tagged for Protein A capture, SPR binding with NRP2, and oriented ELISA coating
• GP1 C-His (VK092021) — for direct plate coating
• GP1 N-His (VK092012) — alternative orientation for epitope accessibility
• Anti-GP1 polyclonal antibody (VK092014)

Glycoprotein GP2 — Class I Fusion Subunit
GP2 is the transmembrane fusion subunit containing the fusion peptide and HR1/HR2 heptad repeats. Anti-GP2 antibodies can block the pre-hairpin intermediate during pH-triggered membrane fusion. Available: GP2 recombinant protein N-His (VK092032) and anti-GP2 polyclonal antibody (VK092034).

Z Protein (Matrix / RING Domain)
Z is the RING-domain matrix protein that drives LUJV budding by recruiting the ESCRT machinery, analogous to VP40 in filoviruses and Z proteins in other arenaviruses. Z is a potential target for budding inhibitors. Available: Z recombinant protein N-GST&C-His (VK092022) and anti-Z polyclonal antibody (VK092024).

Frequently Asked Questions

What makes Lujo virus unique among arenaviruses?
LUJV is exceptional in three ways: (1) it uses neuropilin-2 (NRP2), not α-dystroglycan, as its entry receptor — the only Old World arenavirus known to do so; (2) its 80% case fatality rate is among the highest for any arenavirus; (3) it caused efficient nosocomial person-to-person transmission, unlike most arenaviruses which primarily spread from rodent reservoirs. These features make LUJV a high-priority pathogen for pandemic preparedness.

Do LUJV reagents cross-react with LASV or LCMV?
LUJV is phylogenetically distant from both LASV (Old World, lineage IV) and LCMV, with GP1 amino acid identity of only ~15–25%. Cross-reactivity is not expected. For LASV-specific and LCMV-specific reagents, see our Lassa page and LCMV page.

Can I work with these reagents at BSL-2?
Yes. All LUJV products are recombinant proteins and antibodies — no live or inactivated virus. Standard BSL-1/BSL-2 conditions are sufficient. Live LUJV requires BSL-4.

Related Arenavirus & Hemorrhagic Fever Reagents

Explore reagents for related arenaviruses:

Lassa (LASV) LCMV Junin (JUNV) / Machupo (MACV) Lujo (LUJV) ✓ Ebola (EBOV) CCHFV

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