The construction and assay of hybrid bimodular units with synthetic PKS genes were recently reported.
A sensitive electrochemical method for detection of DNA methylation and assay of DNA methyltransferase (Dam) was investigated based on methylation-sensitive restriction endonuclease, DNA-Au bar bar code and enzymatic signal amplification.
These include the collection, handling and assay of specimens and the design of laboratories to routinely and reliably detect low levels of nucleic acid sequences.
Hydrogel glycan microchips were used for quantitative assay of antibodies against blood group antigens and assay of lectins with fluorescent detection.
Non-destructive detection and assay of nuclear materials is one of the most critical issues for both the management of nuclear waste and the non-proliferation of nuclear materials.
They cannot only be used for affinity purification but also downstream for detection and assay of an arbitrary fused recombinant protein without the need for any prior knowledge of its biochemical properties.
The validity of the proposed methods was examined by analysis of different laboratory prepared mixtures of ORPH, CAF and ASP and assay of their tablet formulation where reliable results were obtained.
Serum samples were collected to assay levels of amylase enzyme, C-reactive protein, IL-6, catalase enzyme activity, malondialdehyde and pancreases were excised for histopathological examination and assay of pancreatic myeloperoxidase.
Virus-induced gene silencing is being used to screen candidate genes for their involvement in MIA biosynthesis, and the function of selected genes can be identified by the expression and assay of recombinant proteins in bacterial or yeast systems.
Incubation of macrophages with forskolin triggered the activation of Akt, predominantly by phosphorylation of Ser-473, as measured by Western blotting and assay of its kinase activity.
The described and successfully tested analytical method, in the case of C. annuum allows, with little modifications if needed, the isolation and assay of the two components even in presence of a large quantity of "ballast" components.
