Abstract: A method is provided for identifying one or more regions within a genome of an organism of interest that mediate the expression of one or more genes of interest.

Abstract: The present invention provides methods and constructs for increasing recombinant protein production in plants during dehydration stress. The invention includes nucleic acids, inducible expression systems, and methods for using same for increasing recombinant protein production in plants and plant protection.

Abstract: The present invention relates to transgenic plants for producing cellulose by a mechanism of autohydrolysis and a method producing soluble sugars using them, more particularly to transgenic plants transformed with recombinant cDNA coding cellulase, cellulose binding domain and chloroplast targeting peptide and a method producing soluble sugars using them. Transgenic plants and a method producing soluble sugars using them would be a highly cost-effective system for the production of soluble sugars on a large scale.

Abstract: The invention pertains to a method for identifying one or more regions within a genome of an organism of interest that mediate the expression of one or more genes of interest. The method comprises identifying a first and a second organism of interest, the first organism of interest is characterized by exhibiting a measurable response to an environmental stimulus, or otherwise, exhibiting a phenotype associated with differential gene expression associated with a process of interest. The second organism of interest is characterized by lacking or not exhibit as strong a response to the stimulus as that observed within the first organism of interest, or it exhibits a different phenotype compared with that of the first organism of interest, wherein the different phenotype is associated with the process of interest, or it exhibits a phenotype of interest that segregates when compared with the first organism of interest, or a combination thereof.

Abstract: The present invention relates to transgenic plants for producing cellulose by a mechanism of autohydrolysis and a method producing soluble sugars using them, more particularly to transgenic plants transformed with recombinant cDNA coding cellulase, cellulose binding domain and chloroplast targeting peptide and a method producing soluble sugars using them. Transgenic plants and a method producing soluble sugars using them would be a highly cost-effective system for the production of soluble sugars on a large scale.

Abstract: The invention pertains to a method for identifying one or more regions within a genome of an organism of interest that mediate the expression of one or more genes of interest The method comprises identifying a first and a second organism of interest, the first organism of interest is characterized by exhibiting a measurable response to an environmental stimulus, or otherwise exhibiting a phenotype associated with differential gene expression associated with a process of interest. The second organism of interest is characterized by lacking or not exhibit as strong a response to the stimulus as that observed within the first organism of interest, or it exhibits a different phenotype compared with that of the first organism of interest, wherein the different phenotype is associated with the process of interest or it exhibits a phenotype of interest that segregates when compared with the first organism of interest, or a combination thereof.

Abstract: This invention is directed to characterizing a host system suitable for the production of functional transgenic proteins, such as anti-human IgG, for use in applications requiring Government regulatory approval. It is well known that regulatory agencies required stable, consistent master cell banks and master cell lines for the production of transgenic proteins in order to ensure sufficient material for appropriate characterization, clinical trials, and potential sales. Current plant production systems require the establishment of seed banks for this purpose. However, there are many draw backs related to such a system for the production of a continuous reliable transgenic protein source. An aspect of this invention is directed to characterizing a plant production system suitable for transgenic proteins that meet the stringent regulatory requirements.