In practice, the competitive diffusion of Evolutionary Trace Annotations via a global network of local evolutionary and structural similarities provides a highly specific and reliable method to predict the function of novel protein structures.
The need for a rapid, specific, sensitive and reliable method to detect this spoilage yeast has increased over the last decade.
However, any investigation aimed at characterizing mucosal immunoglobulins strongly needs specific and reliable methods to achieve solid and reproducible results [17], [19].
We describe here a simple and reliable method to generate large numbers of oligodendroglial progenitors from a renewable source of somatic, non-immortalized hNSCs by exposure to a specific combination of growth factors, neurotrophins and hormones.
Specific, effective and reliable methods to study local immunity are key items in understanding host mucosal response.
However contact map representations require fast and reliable methods to reconstruct the specific folding of the protein backbone.
Therefore, there is an urgent need to develop a rapid, specific and reliable method for the early diagnosis of OS.
Hence, retargeting positions identified in TRACER with a transgene of interest should provide a reliable method to create new tissue- and cell-type specific transgenes.
In this paper, we describe a simple, rapid, specific, sensitive, and reliable method, the FICP method (Fluorescence Immunoassay for Cellular Protein detection) which is readily applicable to the detection of proteins directly on cells cultured in 96-well plates.
In-shoe embedded US is a reliable method to establish person-specific functional geometry of plantar soft tissues.
