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Furthermore, by targeted genetic modification PrV has been developed into a powerful vector system for expression of foreign genes to vaccinate against several infectious diseases of swine, while heterologous vector systems have been used for expression of major immunogens of PrV.
Gabor filters have been used for expression classification in[4, 20].
The NICE system has already been used for expression of soluble plant proteins, like the Arabidopsis coumarate CoA ligase [8] and the strawberry alcohol acyltransferase and linalool/nerolidol synthase [65].
Therefore several expression systems such as E.coli [5], transgenic plant [6], yeast [7], adenovirus vector [8] [12], vaccinia virus vector [13], and DNA vaccine [14], have been used for expression of FMDV antigen to prepare subunit vaccines.
Candidate genes which have been used for expression analysis were in bold fonts.
Because of such unique advantages, transgenic chloroplasts have been used for expression of human therapeutic proteins [ 30- 40, 44].
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The unc-31 promoter was used for expression in neurons and the ges-1 promoter was used for expression in the intestine.
The methylotrophic yeast Pichia pastoris is used for expression of pharmaceutical proteins like 1-8del MCP-1 and vMIP-II.
CHO cells cultured in suspension were used for expression of latent IFN-β to allow medium scale transient transfection.
Here, the MOX promoter derived from another key gene of methanol metabolism is used for expression control.
The combination of these features is used for expression classification.
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