Recombinant West Nile Virus Pre-M Protein


Catalog Number: B2012358 (100 ug)
Recombinant West Nile Virus Pre-M Protein is a high quality Recombinant West Nile Virus Pre-M Protein produced in E. coli. This product has been used as molecular tool for various biochemical applications. It has also been used in a wide array of other chemical and immunological applications. Custom bulk amounts of this product are available upon request.

Live enquiry about this product via Text/SMS: 1-858-900-3210.

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SKU: B2012358 Categories: , Tag:


Recombinant West Nile Virus Pre-M Protein
Catalog number: B2012358
Lot number: Batch Dependent
Expiration Date: Batch dependent
Amount: 100 ug
Molecular Weight or Concentration: 20 kDa
Supplied as: Solution
Applications: molecular tool for various biochemical applications
Storage: -20°C
Keywords: West Nile Virus Pre-M Protein
Grade: Biotechnology grade. All products are highly pure. All solutions are made with Type I ultrapure water (resistivity >18 MΩ-cm) and are filtered through 0.22 um.

1: Wengler G, Wengler G. Cell-associated West Nile flavivirus is covered with E+pre-M protein heterodimers which are destroyed and reorganized by proteolytic cleavage during virus release J Virol. 1989 Jun;63(6):2521-6.
2: Nowak T, Färber PM, Wengler G, Wengler G. Analyses of the terminal sequences of West Nile virus structural proteins and of the in vitro translation of these proteins allow the proposal of a complete scheme of the proteolytic cleavages involved in their synthesis Virology. 1989 Apr;169(2):365-76.
3: Chen WR, Rico-Hesse R, Tesh RB. A new genotype of Japanese encephalitis virus from Indonesia Am J Trop Med Hyg. 1992 Jul;47(1):61-9.
4: Nowak T, Wengler G. Analysis of disulfides present in the membrane proteins of the West Nile flavivirus Virology. 1987 Jan;156(1):127-37.
5: Wengler G, Wengler G, Nowak T, Castle E. Description of a procedure which allows isolation of viral nonstructural proteins from BHK vertebrate cells infected with the West Nile flavivirus in a state which allows their direct chemical characterization Virology. 1990 Aug;177(2):795-801.
6: Wengler G, Wengler G, Nowak T, Wahn K. Analysis of the influence of proteolytic cleavage on the structural organization of the surface of the West Nile flavivirus leads to the isolation of a protease-resistant E protein oligomer from the viral surface Virology. 1987 Sep;160(1):210-9.
7: Pletnev AG, Iamshchikov VF, Blinov VM. [Nucleotide sequence of the genome region of the tick-borne encephalitis virus coding for structural virion proteins] Bioorg Khim. 1986 Sep;12(9):1189-202.
8: Rossi SL, Ross TM, Evans JD. West Nile virus Clin Lab Med. 2010 Mar;30(1):47-65.
9: Hadfield J, Brito AF, Swetnam DM, Vogels CBF, Tokarz RE, Andersen KG, Smith RC, Bedford T, Grubaugh ND. Twenty years of West Nile virus spread and evolution in the Americas visualized by Nextstrain PLoS Pathog. 2019 Oct 31;15(10):e1008042.
10: Bundesgesundheitsblatt Gesundheitsforschung Gesundheitsschutz. 2012 Aug;55(8):1024-43. doi: 10.1007/s00103-012-1507-2. [West Nile virus] Bundesgesundheitsblatt Gesundheitsforschung Gesundheitsschutz

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