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Brand: ProteoGenix

Rabies virus (RABV) Nucleocapsid (NP) ELISA Kit

Assay type:
Quantitative
Detection method:
Colorimetric
Recovery:
80-120%

$893.00

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Rabies virus (RABV) Nucleocapsid (NP) ELISA Kit

Rabies virus (RABV) Nucleocapsid (NP) ELISA Kit

Product name Rabies virus (RABV) Nucleocapsid (NP) ELISA Kit
Delivery condition Blue ice (+4°C)
Delivery lead time in business days 3-5 days if in stocks, 3-5 weeks if production is needed
Storage condition 4°C for short term (1 week), store at -20°C to -80°C for long term(1 year); Avoid repeated freeze-thaw cycles
Brand ProteoGenix
Note For research use only.
Immunogen Nucleocapsid
Assay type Quantitative
Detection method Colorimetric
Recovery 80-120%

Introduction to RABV Nucleocapsid (NP) ELISA Kit

The Rabies virus (RABV) is a deadly virus that is transmitted through the bite of an infected animal. It causes acute encephalitis (inflammation of the brain) and is responsible for thousands of human deaths every year. The Nucleocapsid (NP) protein is a key component of the RABV and plays an important role in the replication and pathogenesis of the virus. The RABV NP ELISA Kit is a valuable tool for researchers and clinicians studying the virus and its potential therapeutic targets.

Structure of RABV Nucleocapsid (NP) Protein

The RABV NP protein is a highly conserved, 30-kDa protein that is essential for the replication and assembly of the virus. It is composed of 265 amino acids and contains two functional domains – a central RNA binding domain and a C-terminal oligomerization domain. The RNA binding domain is responsible for binding to viral RNA and the oligomerization domain is important for the formation of the viral nucleocapsid. The NP protein is also known to interact with other viral proteins and host factors, making it a potential therapeutic target for inhibiting viral replication.

Activity of RABV Nucleocapsid (NP) Protein

The RABV NP protein plays a crucial role in the viral life cycle. It is involved in the encapsidation of the viral genome, which is essential for viral replication. The NP protein also plays a role in viral transcription and translation, as it binds to viral RNA and facilitates its translation into viral proteins. Additionally, the NP protein is involved in the assembly of the viral nucleocapsid, which is the structural component of the virus. This process is essential for the formation of new viral particles and the spread of the virus to new hosts.

Application of RABV Nucleocapsid (NP) ELISA Kit

The RABV NP ELISA Kit is a powerful tool for studying the activity and function of the NP protein. It is a highly sensitive and specific assay that allows for the quantitative measurement of NP protein levels in various samples, such as infected cell lysates or animal tissues. This kit utilizes an enzyme-linked immunosorbent assay (ELISA) technique, which involves the use of specific antibodies to detect and quantify the NP protein.

The RABV NP ELISA Kit has several applications in research and clinical settings. It can be used to study the expression and localization of the NP protein in infected cells or tissues, providing valuable insights into the viral life cycle and pathogenesis. The kit can also be used to screen potential antiviral compounds that target the NP protein, making it a valuable tool for drug discovery and development. Furthermore, the RABV NP ELISA Kit can be used to monitor the efficacy of vaccines and other therapeutic interventions in animal models.

Therapeutic Target for RABV Nucleocapsid (NP) Protein

The RABV NP protein has been identified as a potential therapeutic target for the development of antiviral drugs. As mentioned earlier, the NP protein is essential for the replication and assembly of the virus, making it an attractive target for inhibiting viral replication. In addition, the NP protein is highly conserved among different strains of RABV, making it a promising target for broad-spectrum antiviral therapies.

Several studies have shown promising results in targeting the NP protein for the treatment of RABV infection. For example, a study published in the Journal of Virology demonstrated the effectiveness of a peptide inhibitor that targets the RNA binding domain of the NP protein, leading to a significant reduction in viral replication. This highlights the potential of the RABV NP protein as a therapeutic target for the development of effective antiviral therapies.

Conclusion

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