TBEV gE middle

Tick-Borne Encephalitis Virus gE Middle Recombinant
Cat. No.
BT7188
Source
Escherichia Coli.
Synonyms
Appearance

Sterile Filtered clear solution.

Purity
Encephalitis protein is >95% pure as determined by 10% PAGE (coomassie staining).
Usage
THE BioTek's products are furnished for LABORATORY RESEARCH USE ONLY. The product may not be used as drugs, agricultural or pesticidal products, food additives or household chemicals.
Shipped with Ice Packs
In Stock

Description

The E.coli derived recombinant protein contains the Tick-borne Encephalitis Virus glycoprotein E middle regions, 50-250 amino acids.

Product Specs

Introduction
Tick-borne encephalitis (TBE) is caused by the tick-borne encephalitis virus (TBEV), a member of the Flaviviridae family. A closely related virus found in Far Eastern Eurasia is the Russian spring-summer encephalitis virus (RSSEV). The Flaviviridae family also includes other tick-borne viruses closely related to TBEV and RSSEV, such as the Omsk hemorrhagic fever virus and Kyasanur Forest virus. Louping ill virus is also a member of this family.
Description
This recombinant protein, derived from E. coli, contains the middle region (amino acids 50-250) of the Tick-borne Encephalitis Virus glycoprotein E.
Purity
The purity of the encephalitis protein is greater than 95%, as determined by 10% PAGE (Coomassie staining).
Physical Appearance
Sterile Filtered clear solution.
Formulation
20mM MES pH 6.5, 8M urea, 200mM NaCl, and 0.05% Tween-20.
Stability
While the encephalitis protein remains stable at 4°C for up to one week, it is recommended to store it below -18°C to ensure long-term stability. Avoid repeated freeze-thaw cycles.
Applications
The encephalitis antigen is suitable for use in ELISA and Western blots. It serves as an excellent antigen for detecting the Tick-borne encephalitis virus with minimal specificity issues.
Source
Escherichia Coli.
Purification Method
Encephalitis protein was purified by proprietary chromatographic technique.
Specificity
Immunoreactive with sera of encephalitis virus infected individuals.

Product Science Overview

Introduction

Tick-Borne Encephalitis Virus (TBEV) is a significant pathogen within the Flaviviridae family, responsible for causing tick-borne encephalitis (TBE), a severe neurological disease. TBEV is primarily transmitted through the bite of infected ticks, particularly Ixodes ricinus and Ixodes persulcatus. The virus is endemic in various regions, including Central and Eastern Europe, Russia, and parts of Asia .

Structure and Function of TBEV

TBEV is a positive-sense, single-stranded RNA virus. The viral genome encodes three structural proteins: the capsid ©, membrane (M), and envelope (E) proteins. The envelope (E) protein is particularly crucial as it mediates viral entry into host cells and is the primary target for neutralizing antibodies .

Recombinant gE Middle Protein

The gE Middle recombinant protein refers to a specific segment of the TBEV envelope (E) protein. This recombinant protein is engineered to include the middle portion of the E protein, which is essential for the virus’s ability to infect host cells and elicit an immune response. The recombinant gE Middle protein is often used in research and vaccine development to study the virus’s pathogenic mechanisms and to develop effective vaccines .

Importance in Vaccine Development

The gE Middle recombinant protein plays a pivotal role in vaccine development against TBEV. By focusing on this segment of the E protein, researchers aim to create vaccines that can induce a robust immune response, providing protection against the virus. The recombinant protein is used to evaluate the efficacy of potential vaccines and to understand the immune mechanisms involved in protection .

Research and Findings

Studies have shown that the envelope protein of TBEV, including the gE Middle segment, significantly influences the virus’s ability to enter neurons, its pathogenicity, and the effectiveness of vaccines. For instance, specific amino acid substitutions in the E protein can enhance the virus’s neurovirulence and replication in vivo . These findings underscore the importance of the gE Middle recombinant protein in understanding TBEV’s behavior and developing effective countermeasures.

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