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Accelerated progress in the use of droplet-based microfluidics for high throughput screening and biochemical analysis will require development of devices that are robust to experimental uncertainties and which offer multiple functionalities.
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Besides ultrastructural and biochemical studies and the information on the metabolic role in other plant species of phylogenetically related genes, the functional analysis will require the selective silencing of the PDI and PDI-like genes in wheat plants and the characterization of the regulatory motifs through the expression studies of the progressive deletions of their promoters.
Full statistical analysis will require a larger cohort.
Future biochemical analysis will be required to show that human Zwint-1 and hSPC105 form a heterotrimer.
In addition, we show that Cora co-immunoprecipitates with Dg, indicating the presence of the two proteins in the same complex, although further biochemical analysis will be required to assess whether they interact directly or indirectly.
Further genetic and biochemical analysis will be required to distinguish among these possibilities.
Detailed biochemical analysis will be needed to explore these possibilities.
All biochemical analysis will also be conducted blinded to treatment group.
Furthermore, no other measure or biochemical analysis will give such information.
Cross-platform analyses of biochemical pathway data will require additional data processing and novel computational bioinformatics tools to address unique statistical challenges.
This was a post-hoc analysis that will require replication.
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