GLOBAL POINT OF CARE
GLOBAL POINT OF CARE
The Panbio™ Dengue Early Rapid is a dengue NS1 antigen serum, plasma or whole blood immunochromatographic assay. It is for the qualitative detection of NS1 antigen in serum, plasma or whole blood used as an aid in the clinical laboratory diagnosis of patients with clinical symptoms consistent with dengue fever. The Panbio™ Dengue Early Rapid should be used in conjunction with other dengue serology tests.
Product not available in all countries. Please check with your local sales representative regarding availability in your area.
1. Libraty DH, Young PR, Pickering D, Endy TP, Kalayanarooj S, Green S, Vaugh OW, Nisalak A, Ennis FA and Rothman AL. (2002). High circulating levels of the dengue virus non-structural protein NS1 early in dengue illness correlate with the development of dengue haemorrhagic fever. J Infect Dis. 186:1165-1168.
2. Alcon S, Talarmin A, Debruyne M, Falconar A, Deubel V,and Flammand M (2002). Enzyme-linked immunosorbent assay specific to dengue virus type 1 nonstructural protein NS1 reveals circulation of the antigen in the blood during the acute phase of disease in patients experiencing primary or secondary infections. J Clin Microbiol. 40:376-381.
3. Young PR, Hilditch PA Bletchly C and Halloran W. (2000). An antigen capture enzyme-linked immunosorbent assay reveals high levels of the dengue virus protein NS1 in the sera of infected patients. J Clin Microbiol. 38:1053-1057.
4. Lindegren G, Vene S, Lundkvist A and Falk KI. (2005). Optimized diagnosis of acute dengue fever in Swedish travelers by a combination of reverse transcription-PCR and Immunoglobulin M detection. J Clin Microbiol. 412850-2855.
5. Shu P and Huang J. (2004). Current advances in dengue diagnosis. Clin Diagn Lab Immunol. 11:642-650.
6. Fry S, e al (2011). The Diagnostic Sensitivity of Dengue Rapid Test Assays is Significantly Enhanced by Using a Combined Antigen and Antibody Testing Approach. PLoS Negl Trop Dis 5(6y, 199. doi:10.1371/journal.pntd.0001199.
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Not all products are available in all regions. Check with your local representative for availability in specific markets. For in vitro diagnostic use only. For i-STAT test cartridge information and intended use, refer to individual product pages or the cartridge information (CTI/IFU) in the i-STAT Support area.
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