Author: Suthar, Mehul S.; Ma, Daphne Y.; Thomas, Sunil; Lund, Jennifer M.; Zhang, Nu; Daffis, Stephane; Rudensky, Alexander Y.; Bevan, Michael J.; Clark, Edward A.; Kaja, Murali-Krishna; Diamond, Michael S.; Gale, Michael
Title: IPS-1 Is Essential for the Control of West Nile Virus Infection and Immunity Document date: 2010_2_5
ID: 094d0rn6_49
Snippet: WNV-specific IgM, total IgG, IgG1, and IgG2a levels were determined by an ELISA using purified recombinant E protein as previously described [55] . The neutralization titer of serum antibody was determined by using a previously described plaque reduction neutralization assay [40] . Briefly, sera samples from mock or WN-TX infected mice were diluted in DMEM followed by incubation at 56uC for 30 minutes to inactivate virus and complement factors. S.....
Document: WNV-specific IgM, total IgG, IgG1, and IgG2a levels were determined by an ELISA using purified recombinant E protein as previously described [55] . The neutralization titer of serum antibody was determined by using a previously described plaque reduction neutralization assay [40] . Briefly, sera samples from mock or WN-TX infected mice were diluted in DMEM followed by incubation at 56uC for 30 minutes to inactivate virus and complement factors. Sera were further diluted in two-fold increments and incubated with 100 PFU of WN-TX at 37uC for 1 hour. Standard plaque assays were performed on BHK21 cells and the dilution at which 50% of plaques were neutralized was determined by comparing the number of plaques formed from WNV-infected sera samples to mock infected sera samples.
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