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Chromatin Immuno Precipitation (ChIP) is a biochemical method to identify binding sites on DNA that interact with proteins.
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Rudra and colleagues [ 24] used biochemical methods to identify the FOXP3 interactome.
In this paper hybrid delay differential equations with discrete time series was determined to be a powerful method to identify delayed dynamics of ill-defined biochemical networks.
Sequence-based identification is an alternative method to identify clinical isolates that are either slow growers or difficult to identify by biochemical profiling.
We used standard biochemical and serological methods to identify NTS, which were then stored at –80°C.
To further understand the characteristics and functions of intercellular bridges, we used a previously developed biochemical method to enrich intercellular bridges from mouse testes to identify new intercellular bridge proteins [14].
These observations support the results presented by Ma et al. [ 22] who used computational methods to identify network topologies that can achieve biochemical adaptation.
In particular, we are interested in using computational methods to identify novel eukaryote-specific proteins that may be involved in RNA metabolism and predicting their potential biochemical functions.
He and three colleagues used light and electron microscopes, as well as biochemical methods, to examine the tissues.
The biochemical method was used to identify the species of group B streptococci[ 15- 17].
Conventional biochemical methods are able to identify mycobacterial species; but they are tedious and time consuming and require elaborate safety precautions.
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