Summary
| Production Name | Anti-Langya virus/LayV M/Matrix protein Polyclonal Antibody |
| Description | Rabbit polyclonal Antibody |
| Host | Rabbit |
| Application | ELISA, IHC, WB |
| Reactivity | Wenzhou Apodemus agrarius henipavirus 1, Mojiang virus, Wenzhou shrew henipavirus 1, Langya virus, Crocidura olivieri henipavirus 1, Lechcodon virus, Hasua virus |
Performance
| Conjugation | Unconjugated |
| Modification | Unmodified |
| Isotype | IgG |
| Clonality | Polyclonal |
| Form | Liquid |
| Storage | Store at 4°C short term. Aliquot and store at -20°C long term. Avoid freeze/thaw cycles. |
| Buffer | 0.01M PBS, pH 7.4, 50% Glycerol, 0.05% Proclin 300. |
| Purification | Purified by antigen affinity column. |
Immunogen
| Gene Name | Matrix |
| Alternative Names | matrix protein, M |
| Gene ID | |
| SwissProt ID |
Application
| Dilution Ratio | ELISA 1:5000-1:20000 IHC 1:50-1:500 WB 1:500-1:2000 |
| Molecular Weight |
Background
Nipah virus (NiV), a highly pathogenic zoonotic paramyxovirus, mediates host cell entry through the coordinated action of two envelope glycoproteins: the attachment glycoprotein (G), which engages the host cell receptors ephrin-B2 and ephrin-B3, and the fusion glycoprotein (F), which drives membrane fusion following receptor binding. These viral surface proteins, along with the viral RNA-dependent RNA polymerase (RdRp) complex comprising the nucleoprotein (N), phosphoprotein (P), and large polymerase protein (L), constitute the primary molecular targets for therapeutic intervention and vaccine development. The conserved receptor-binding interface of the G protein and the fusion machinery of the F protein represent particularly attractive targets for neutralizing antibodies and entry inhibitors, while the viral replication machinery offers potential targets for broad-spectrum antiviral compounds targeting paramyxovirus transcription and replication.
Research Area
Microbiology&Infectious Disease