Objective Phage particle antigens were used as a model antigen to investigate the potential mechanism of crosspresentation.
目的以噬菌体颗粒抗原为模式抗原，研究其交叉呈递的可能机制。
2
Furthermore, the effect of proteasome inhibitors and TAP on particle antigens crosspresentation was investigated by FACS analysis.
进而，采用流式细胞技术研究了不同蛋白酶体抑制剂以及TAP对噬菌体颗粒抗原交叉呈递的影响。
3
The Servoy environment employs an n-tier architecture which includes cross-database support, and advanced application server, and a variety of deployment options in the presentation layer.