Neuraminidase anticorps

N° du produit ABIN7595320

Cet anticorps anti-Neuraminidase est un anticorps Lapin Polyclonal détectant Neuraminidase dans WB, ELISA et IHC. Adapté pour Influenza A Virus.

Aperçu rapide pour Neuraminidase anticorps (ABIN7595320)

Antigène: Neuraminidase (NA)

Reactivité: Influenza A Virus

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp Neuraminidase est non-conjugé

Application: Western Blotting (WB), ELISA, Immunohistochemistry (IHC)

Détail du produit anti-Neuraminidase anticorps

Virus Strain: A/Chicken/Scotland/1959

Fonction: Rabbit antibody to Influenza A virus Neuraminidase (40...390)

Specificité: Specific for Influenza A virus NA.

Réactivité croisée: Influenza A Virus

Purification: Purified IgG

Immunogène: A chimeric recombinant Neuraminidase from Influenza A virus NA (strain A/Chicken/Scotland/1959 H5N1) containing regions 40-80 140-175 190-230 245-278 and 361-390 was used as the antigen.

Isotype: IgG

Information d'application

Indications d'application: IHC WB ELISA. A dilution of 1 : 1000 is recommended. The optimal dilution should be determined by the end user. Not yet tested in other applications.

Restrictions: For Research Use only

Stockage

Format: Lyophilized

Reconstitution: Reconstitute in 100 µL of sterile water. Centrifuge to remove any insoluble material.

Stock: 4 °C,-20 °C

Stockage commentaire: Maintain the lyophilised/reconstituted antibodies frozen at -20°C for long term storage and refrigerated at 2-8C for a shorter term. 

Date de péremption: 12 months

Détails sur Neuraminidase

Antigène: Neuraminidase (NA)

Autre désignation: Neuraminidase

Classe de substances: Influenza Protein

Sujet: Function: Catalyzes the removal of terminal sialic acid residues from viral and cellular glycoconjugates. Cleaves off the terminal sialic acids on the glycosylated HA during virus budding to facilitate virus release. Additionally helps virus spread through the circulation by further removing sialic acids from the cell surface. These cleavages prevent self-aggregation and ensure the efficient spread of the progeny virus from cell to cell. Otherwise infection would be limited to one round of replication. Described as a receptor-destroying enzyme because it cleaves a terminal sialic acid from the cellular receptors. May facilitate viral invasion of the upper airways by cleaving the sialic acid moieties on the mucin of the airway epithelial cells. Likely to plays a role in the budding process through its association with lipid rafts during intracellular transport. May additionally display a raft-association independent effect on budding. Plays a role in the determination of host range restriction on replication and virulence. Sialidase activity in late endosome/lysosome traffic seems to enhance virus replication.