Monkeypox
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Project Description

Holistic Preclinical Research for Tanapox & Yana-Like Virus Therapeutic Development & Diagnostic Innovation

Overview

Tanapox virus (TANV), along with Yana-like viruses, is categorized within the Poxviridae family. They mainly infect primates, but ongoing research determines their human disease potential. The Tanapox virus, originally discovered in East Africa, produces a mild disease like pox, which presents with fever and skin lesions followed by lymph node swelling. Yana-like viruses share structural similarities with Tanapox virus, yet remain understudied. Infected animals can spread these viruses to humans, which makes them potential zoonotic threats. The limited understanding of the molecular biology and pathogenesis of Tanapox and Yana-like viruses complicates both drug development and diagnostic processes. Therapeutic development and diagnostic effectiveness depend on understanding the viral lifecycle alongside immune responses and animal model potential. Creative Biolabs' preclinical research services provide detailed support for Tanapox and Yana-like viruses through virus characterization methods, along with animal model development and therapeutic screening processes. Our services drive the advancement of drug discovery and diagnostics by supplying vital data that speeds up the creation of safe and effective treatments. Through our knowledge of viral pathogenesis and immunology, we achieve strong preclinical research that supports upcoming clinical studies.

Accelerated Tanapox and Yana-Like Disease Virus Preclinical Research Services

  • For Therapeutics Development

In Vitro Antiviral Efficacy Assays

  • Cytotoxicity Assay: To determine the maximum safe concentration of the therapeutic candidate by assessing its toxicity to cells.
  • Viral Replication Inhibition Assay: Measures the ability of the therapeutic candidate to inhibit viral replication in cultured cells.
  • Plaque Assay/TCID50: Quantifies the reduction in viral titers in infected cells after treatment with the therapeutic compound.
  • Mechanism of Action Studies: Assesses whether the drug targets viral entry, replication, or other stages of the viral life cycle (e.g., viral fusion inhibitors, protease inhibitors).
  • IC50/EC50 Determination: Determines the concentration at which the drug inhibits 50% of the viral replication or viral infection, used to gauge potency.

In Vivo Efficacy Studies (Animal Models)

  • Efficacy Evaluation: Measure the clinical signs, survival rate, viral load, and organ pathology in animals treated with the therapeutic compound.
  • Pharmacokinetics: Evaluate how the drug is absorbed, distributed, metabolized, and excreted in the body.
  • Viral Load Assessment: Quantification of viral titers in tissues (e.g., blood, organs) at different time points to assess viral clearance.
  • Immune Response Analysis: Measurement of immune responses such as cytokine release, T-cell activity, antibody production, and the overall immunological impact of the therapeutic.
  • Dose-Response Studies: To determine the optimal dosage that produces the best therapeutic outcome with minimal side effects.
  • Toxicity Studies: Long-term toxicity and safety profile determination, including organ histopathology and biochemistry panels to evaluate any adverse effects.
  • For Diagnostics Development

Antigen Detection Assays

  • Immunohistochemistry (IHC): Uses antibodies to detect viral antigens in tissue sections, enabling the localization of TANV in different tissues (such as infected organs in animal models).
  • Western Blotting: Detects viral antigens by separating proteins through gel electrophoresis and using antibodies to identify specific viral proteins.

Nucleic Acid Detection Assays

  • Nested PCR: Enhances the sensitivity of PCR detection, used for low-abundance viral genomes.
  • Nucleic Acid Hybridization Assay (DNA/RNA Probes): Detects viral DNA or RNA by using a labeled probe that binds specifically to the viral nucleic acid sequence.
  • Loop-Mediated Isothermal Amplification (LAMP): A more rapid and cost-effective alternative to PCR for detecting viral nucleic acids at constant temperatures.

Antibody Detection Assays (Serology)

  • Western Blotting (Serological Confirmation): Detects specific antibodies against viral proteins. It is often used for confirmatory testing, especially when ELISA results are ambiguous.
  • Neutralization Assays: Detects the presence of neutralizing antibodies, which are crucial for immunity and the potential for therapeutic development.
  • Immunofluorescence Assay (IFA): Detects specific antibodies against viral antigens by using fluorescently labeled secondary antibodies.
  • Rapid Diagnostic Test (RDT) Kits: Lateral flow immunoassays that can detect antibodies or antigens quickly.

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Products for Tanapox and Yana-Like Disease Virus Research

At present, specialized products for Tanapox and Yana-like virus research remain scarce. The available reagents designed for viral genome examination, including PCR kits along with antibodies that assist in antigen detection and serological research.

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Applications

  • Viral Pathogenesis Studies

Tanapox and Yana-like viruses serve as important research models to study viral infection processes and replication mechanisms alongside host immune response reactions. The research reveals the interaction mechanisms between poxviruses and host cells, which aids the development of vaccines and therapeutic approaches.

  • Vaccine Development

These viruses help in developing new vaccine strategies due to their close relationship with other poxviruses and their importance for zoonotic viral research. Investigating Tanapox has implications for creating vaccines against similar poxviruses such as smallpox and monkeypox.

  • Antiviral Drug Discovery

The viruses serve as a testing platform for evaluating antiviral compound effectiveness. Research on the replication cycle of these viruses enables scientists to detect possible drug targets that aid in creating treatments for related viral infections.

  • Diagnostic Assay Development

Tanapox and Yana-like viruses are essential for developing diagnostic tools capable of detecting infections in both wildlife and humans because of their zoonotic nature in regions where they naturally occur.

Advantages

1. Comprehensive Expertise: Our research team combines the expertise of virologists with immunologists and diagnostic specialists to adopt a multidisciplinary perspective on virus research. Our team provides extensive expertise in viral pathogenesis research as well as therapeutic development and validation of diagnostic assays.

2. Tailored Research Solutions: Our services include tailored research solutions to meet specific requirements and cover areas such as antiviral drug screening, vaccine development, and diagnostic assay creation. Our adaptable methodology allows every research project to meet specific viral characteristics that need investigation.

3. Advanced Technology & Methodologies: Our research utilizes state-of-the-art technology through PCR assays, next-generation sequencing, cell culture systems, and animal models, which enables us to produce high-quality and reliable results. Our advanced laboratory facilities deliver precise and repeatable outcomes for every scientific investigation.

FAQs

Are custom research services available to meet specific research requirements?

We deliver customized research solutions that meet your requirements. We work alongside you to create research projects that match your goals through close collaboration when you need custom antiviral screening or specialized diagnostic assay development.

How much do your research services cost?

Our service fees are calculated based on the research scope and the services needed. Our quotes are individually tailored according to both your project needs and its overall size. Reach out to us for a comprehensive discussion, after which we will supply you with a cost estimate.

Would you like support for validating diagnostic assays to secure regulatory approval?

We help with diagnostic assay validation to ensure they meet regulatory standards while becoming accurate and reliable for clinical use. Our team possesses expertise in collaborating with health authorities for successful assay approval.

What steps should I follow to begin working with your virus research services?

You can begin by sending us a message through our contact form or by making a phone call. We will set up a meeting to evaluate your research requirements while preparing a project proposal and outlining subsequent planning stages to advance your research.

We DO NOT PROVIDE ANY PRODUCTS OR SERVICES DIRECTLY TO PATIENTS. All of our products are for Research Use Only (RUO), NOT intended for diagnostic, therapeutic, or clinical use.

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