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TheNativeAntigenCompany/Chikungunya Virus IgM capture ELISA/ELS61243

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货号:ELS61243
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商品描述

CHIKUNGUNYA VIRUS IgM CAPTURE ELISA

This Chikungunya virus IgM capture ELISA kit has been designed for the detection and the quantitative determination of specific IgM antibodies against Chikungunya virus in human serum or plasma.

This ELISA is based on the mu-capture principle. Microplates are coated with anti-human IgM to capture IgM antibodies within the sample. After washing the wells to remove all unbound sample material, horseradish peroxidase labelled Chikungunya virus antigen conjugate is added. This conjugate binds to the captured Chikungunya virus-specific antibodies. The immune complex formed by the bound conjugate is visualized with Tetramethylbenzidine (TMB) substrate which gives a blue reaction product. The intensity of this product is proportional to the amount of specific antibodies in the sample. Sulphuric acid is added to stop the reaction. This produces a yellow endpoint colour. Absorbance at 450/620 nm is read using an ELISA microwell plate reader.

PRODUCT DETAILS – CHIKUNGUNYA VIRUS IgM CAPTURE ELISA

  • Chikungunya Virus IgM µ-capture ELISA.
  • High sensitivity – 100%.
  • High specificity – 100%.
  • Short assay time – <3 hours.
  • 1 x 96 tests.

BACKGROUND

Chikungunya virus is an arthropod borne virus of the genus Alphavirus (family Togaviridae). The Alphavirus genus contains at least 24 distinct species. These are lipid-enveloped virions with a diameter of 50 to 60 nm. Alphavirus infections are initiated by the bite of an infected mosquito, which results in the deposition of virus in subcutaneous and possibly cutaneous tissues. After an incubation period of 1 to 12 days the Chikungunya fever develops. Chikungunya fever (Chikungunya means “that which bends up”, in reference to the crippling manifestations of the disease) is an acute viral infection characterized by a rapid transition from a state of good health to illness that includes severe arthralgia and fever.

Temperature rises abruptly to as high as 40 °C and is often accompanied by shaking chills. After a few days, fever may abate and recrudesce, giving rise to a “saddleback” fever curve. Arthralgia is polyarticular, favoring the small joints and sites of previous injuries, and is most intense on arising. Patients typically avoid movement as much as possible. Joints may swell without significant fluid accumulations. These symptoms may last from 1 week to several months and are accompanied by myalgia. The rash characteristically appears on the first day of illness, but onset may be delayed. It usually arises as a flush over the face and neck, which evolves to a maculopapular or macular form that may be pruritic. The latter lesions appear on the trunk, limbs, face, palms and soles, in that order of frequency. Petechial skin lesions have also been noted. Headache, photophobia, retro-orbitral pain, sore throat with objective signs of pharyngitis, nausea and vomiting also occur in this setting. Occasionally, however persistent arthralgia and polyarthritis (lasting months or even years) do occur, sometimes involving joint destruction. Even rarer, sequelae include encephalitis and meningoencephalitis with high lethality rates.

The virus has major importance in Africa and Asia. From 20% to more than 90% of the population of tropical and subtropical show serologic evidence of infection. Because Aedes mosquitoes are increasingly prevalent in North Africa and South America, where the population would be uniformly susceptible to infection, the possibility for epidemics is evident. Chikungunya virus infections are imported to central Europe mainly by travelers to tropical and subtropical countries.

REFERENCES

  • Bienz, Kurt A. (2005): Viruses as Human Pathogen. In Fritz H. Kayser, Kurt A. Bienz, Johannes Eckert, Rolf M. Zinkernagel: Medical microbiology. Stuttgart, New York: Thieme (Thieme Flexibook), pp. 412–474.
  • Hochedez, Patrick; Jaureguiberry, Stephane; Debruyne, Monique; Bossi, Philippe; Hausfater, Pierre; Brucker, Gilles et al. (2006): Chikungunya infection in travelers. In Emerging infectious diseases 12 (10), pp. 1565–1567. DOI: 10.3201/eid1210.060495.
  • Markoff, Lewis (2005): Chapter 147: Alphaviruses. In Gerald L. Mandell, Robert Gordon Douglas, John Eugene Bennett (Eds.): Mandell, Douglas, and Bennett’s principles and practice of infectious diseases, vol. 2. 6. ed. Philadelphia, Pa.: Elsevier, pp. 1913–1920.
  • Weaver, Scott C.; Tesh, Robert B.; Shope, Robert E. (2006): Alphavirus Infections. In Richard L. Guerrant, David H. Walker, Peter F. Weller (Eds.): Tropical infectious diseases. Principles, pathogens & practice. 2nd ed. Philadelphia: Churchill Livingstone, pp. 831–838.

THIS ELISA ASSAY IS FOR RESEARCH USE ONLY. IT IS NOT FOR USE IN DIAGNOSTIC PROCEDURES.

Instructions for useQuickstart guideSafety datasheet

Ambient

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。