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Multi-carrier DS-CDMA has been considered as an eeective scheme for reducing multiple access interference in the case of quasi-synchronous transmission. The scheme allows the reduction of multiple access interference by transferring the or-thogonality property of the signals into the frequency domain where the orthog-onality property is robust to relative(More)
Recombinant plasmids containing the A-segment or VP2/4/3 gene of infectious bursal disease virus (IBDV) were transfected into Vero cells. Monoclonal Vero cell lines were generated under G418 selection. Genomic (PCR/Southern blot) and transcriptional (RT-PCR/Northern blot) analyses showed that one copy of A-segment or VP2/4/3 or a partial gene of them was(More)
MAGE-A3 is highly expressed in many kinds of malignant diseases, and considered to be an ideal candidate for anti-tumor vaccine. To improve the immunogenicity of epitopes of MAGE-A3, hepatitis B virus core antigen (HBcAg) was used as an immune-carrier by insertion epitopes at HBcAg major immunodominant region (HBcAg(MIR)). In present study, we designed(More)
Epstein-Barr virus (EBV) is a human oncogenic herpesvirus associating with several malignant diseases. Latent membrane protein 2 (LMP2) of EBV is considered to be an ideal candidate for immunotherapy or prophylactic EBV vaccine. We designed a LMP2 multiepitope containing T and B-cell epitope-rich peptides and constructed a recombinant plasmid containing(More)
A modified multicarrier (MC) direct-sequence code-division multiple-access (DS-CDMA) system has been proposed for use over slow multipath fading channels with frequency selectivity in the reverse link transmission of a cellular network. Instead of transmitting data substreams uniformly through sub-channels, data substreams hop over subchannels with the(More)
Adeno-associated viruses are members of the genus dependoviruses of the parvoviridae family. AAV vectors are considered promising vectors for gene therapy and genetic vaccination as they can be easily produced, are highly stable and non-pathogenic. Nevertheless, transduction of cells in vitro and in vivo by AAV in the absence of a helper virus is(More)
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