The application notes include recommended starting dilutions; optimal dilutions/concentrations should be determined by the end user.
The p10 fusion-associated small transmembrane protein of avian reovirus
induces extensive syncytium formation in transfected cells. The p10-induced cell-cell fusion is restricted by rapid degradation of the majority of newly synthesized p10. The small ectodomain of p10 targets the protein for degradation following p10 insertion into an early membrane compartment. Paradoxically, conservative amino acid substitutions in the p10 ectodomain hydrophobic patch that eliminate fusion activity also increase p10 stability. The small amount of p10 that escapes intracellular degradation accumulates at the cell surface in a relatively stable form, where it mediates cell-cell fusion as a late-stage event in the virus replication cycle. The unusual relationship between a nonstructural viral membrane fusion protein and the replication cycle of a nonenveloped virus has apparently contributed to the evolution of a novel mechanism for restricting the extent of virus-induced cell-cell fusion.
10 kDa protein antibody
Fusion protein p10 antibody
has not yet been referenced specifically in any publications.
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