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Ons (mannanbinding activity) and MBL C4 cleavage activity in sera from 35 healthy adult volunteers of Caucasian, Asian, Hispanic or AfricanAmerican ancestry (females, n = 20). The sample had a 3.7 log10 range of MBL concentrations (0?,424 ng/mL) that were strongly correlated with the concordant MBL C4 cleavage values (0?7,468 U/mL; r2 = 0.91). The sample included three individuals with homozygous
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Ons (mannanbinding activity) and MBL C4 cleavage activity in sera from 35 healthy adult volunteers of Caucasian, Asian, Hispanic or AfricanAmerican ancestry (females, n = 20). The sample had a 3.7 log10 range of MBL concentrations (0?,424 ng/mL) that were strongly correlated with the concordant MBL C4 cleavage values (0?7,468 U/mL; r2 = 0.91). The sample included three individuals with homozygous
1
Ons (mannanbinding activity) and MBL C4 cleavage activity in sera from 35 healthy adult volunteers of Caucasian, Asian, Hispanic or AfricanAmerican ancestry (females, n = 20). The sample had a 3.7 log10 range of MBL concentrations (0?,424 ng/mL) that were strongly correlated with the concordant MBL C4 cleavage values (0?7,468 U/mL; r2 = 0.91). The sample included three individuals with homozygous
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Exposed to autoradiography film. High-mannose moieties were preserved only in untreated virus confirming that PNGase F and endo H effectively cleaved high-mannose residues on GPs of HIV-EBOV virion-like particles. (EPS) Figure S4 Thermolysin treatment of HIV-EBOV GP abrogates enhancement of infection by rhMBL in a thermolysin-concentration dependent manner. We preincubated HIV-EBOV GP virion-like
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Ons (mannanbinding activity) and MBL C4 cleavage activity in sera from 35 healthy adult volunteers of Caucasian, Asian, Hispanic or AfricanAmerican ancestry (females, n = 20). The sample had a 3.7 log10 range of MBL concentrations (0?,424 ng/mL) that were strongly correlated with the concordant MBL C4 cleavage values (0?7,468 U/mL; r2 = 0.91). The sample included three individuals with homozygous
1
Ons (mannanbinding activity) and MBL C4 cleavage activity in sera from 35 healthy adult volunteers of Caucasian, Asian, Hispanic or AfricanAmerican ancestry (females, n = 20). The sample had a 3.7 log10 range of MBL concentrations (0?,424 ng/mL) that were strongly correlated with the concordant MBL C4 cleavage values (0?7,468 U/mL; r2 = 0.91). The sample included three individuals with homozygous
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On of fetal calf or fetal bovine serum typically used for EBOV infectivity assays [17,18,44,45,67]. Given that C4 gene copy number variations may lead to a proportionate reduction ofLectin-Dependent Enhancement of Ebola Virusesiological doses of MBL products or blood products with high MBL concentrations to individuals in the setting of infectious diseases and relative hypocomplementemia may be de
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Ons (mannanbinding activity) and MBL C4 cleavage activity in sera from 35 healthy adult volunteers of Caucasian, Asian, Hispanic or AfricanAmerican ancestry (females, n = 20). The sample had a 3.7 log10 range of MBL concentrations (0?,424 ng/mL) that were strongly correlated with the concordant MBL C4 cleavage values (0?7,468 U/mL; r2 = 0.91). The sample included three individuals with homozygous