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TheNativeAntigenCompany/Adenovirus Type 5 Particles, Wild-Type/100µl/AD005-100

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货号:AD005-100
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品牌:TheNativeAntigenCompany
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商品描述

ADENOVIRUS TYPE 5 PARTICLES, WILD-TYPE

This product is a concentrated source of highly-purified human Adenovirus type 5 particles (wild-type) from a lysate of optimally-infected 293 cells. Following double CsCl gradient purification with DNase treatment and dialysis, this Ad5 preparation is of very high quality and minimal lot-to-lot variation. This product has been referenced by Thoma, 2013 and Dyer, 2017.

PRODUCT DETAILS – ADENOVIRUS TYPE 5 PARTICLES, WILD-TYPE

  • Wild-type Adenovirus Type 5 particles.
  • Double CsCl gradient purification with DNase treatment and dialysis.
  • Produced in HEK293 cells and stored in pH 7.8 PBS buffer.

BACKGROUND

Adenoviruses are medium-sized (80–100 nm), non-enveloped viruses. They have an icosahedral nucleocapsid containing a linear, double-stranded DNA genome of approximately 36 kb (Nermut, 1984). The viral genome is grouped into different transcriptional units, designated early (E1, E2, E3, E4), intermediate, and late. The E1 gene is essential for activation of other viral genes and for viral replication. Deletion of the E1 gene results in viruses that are replication incompetent in normal cells. However, replication-competent viral particles can be produced from E1-deleted viral vectors by providing the E1 gene in trans.  The E3 gene is nonessential for either viral replication or infection (Flint, 1999).

Wild-type adenoviruses, including human adenovirus type 5, are associated with a number of mild disorders, such as lower respiratory tract infections in the elderly or children. Of the 57 human adenovirus serotypes, 5 (Ad5) is one of the best studied, providing a better understanding of virus biology, host cellular processes and virus-cell interactions during infection. Ad5 is also widely used for transgene delivery in preclinical and clinical gene therapy studies; replication-defective vectors have been described expressing Ebola glycoproteins and malaria antigens for vaccine trials.

REFERENCES

  • Flint, J., 1999. Organization of the adenoviral genome. In: P. Seth, ed. Adenoviruses: Basic Biology to Gene Therapy. Austin, TX, USA: R.G. Landes Company, pp. 17-30.
  • Nermut, M. V., 1984. The Architecture of Adenoviruses. In: . (eds) . In: H. S. Ginsberg, ed. The Adenoviruses. The Viruses. Boston, MA: Springer.
  • Thoma, C. et al. 2013. Adenovirus Serotype 11 Causes Less Long-Term Intraperitoneal Inflammation than Serotype 5: Implications for Ovarian Cancer Therapy. Virology, 74-83. Elsevier.
  • Dyer, A. et al. 2017. Oncolytic Group B Adenovirus Enadenotucirev Mediates Non-apoptotic Cell Death with Membrane Disruption and Release of Inflammatory Mediators. Mol Ther Oncolytics, 18-30. Elsevier.

This material is intended for research purposes only, NOT FOR HUMAN USE. Handle material as a category 2 pathogen using category 2 facilities and procedures.

Certificate of analysisSafety datasheet

TheNativeAntigenCompany我们在测定开发方面拥有多年经验。根据具体应用,我们建议并测试多种不同的ELISA格式,从简单的直接ELISA到具有封闭抗原的间接ELISA和双抗原结合ELISA。您不仅可以从我们的高级测定开发科学家那里获得咨询的好处,而且我们的内部表达系统还可以用于生产天然折叠的和完全糖基化的蛋白质和抗体,以用作最高质量的独特试剂,从而使您的ELISA处于优势反对竞争。我们的能力包括:+   ELISA设计和格式咨询+   定制抗原和抗体生产+   使用定制抗原作为免疫原(mAbs和pAbs)产生抗体+   ELISA中的抗原/抗体对优化+   与酶结合以检测抗体+   板涂+   ELISA优化  我们可以在项目的任何阶段为您的ELISA分析的开发提供支持,  提供定制服务,这些灵活性可以评估用于分析的最佳抗体  对,直至商业套件的全面开发。 如果您的概念还处于早期阶段,那么我们可以准备您的抗原,  提高您的抗体,并使用它们来开发特定的ELISA分析以满足您的需求。