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An important note here: A TAG is not to be confused with hierarchal organization structures, such as the traditional file+folder systems on computers.
Here, a "tag" consisting of a specific amino acid sequence, often a series of histidine residues (a "His-tag"), is attached to one terminus of the protein.
Whereas, previous studies were done on a limited number of SNPs, here, a Tag SNPs approach was applied to catch all the genetic information from each candidate gene.
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Here, a time tag is used to record the storage time information for each memory block or page and this information is used to determine the threshold resistance that minimizes the BER.
Here, a polypeptide tag, which is genetically fused to the target protein, binds to a fluorescently labeled substrate.
Thus, here a temporal tag, instead of an enhanced response, labels image elements to be grouped in perception.
Here, a marker tag enables both the cloning of the active gene and visualization of its activity (Starr et al. 2011).
Here, a script tag is created in which the endpoint from which data is to be received is defined as the src-attribute.
We report here an epitope-tagging strategy for the purification of protein complexes in mouse ESCs.
Here, a modified histidine tag (HE) used as an affinity tag was employed together with a truncated maltotriose-binding protein (MBP; consisting of residues 59 433) from Pyrococcus furiosus as a solubility enhancing tag accompanying a tobacco etch virus protease-recognition site for protein expression and purification in Escherichia coli.
The original vectors were created with a HindIII site for tag cloning (e.g. pSANG-10, Figure 1a) and, in the bulk of the work described here, a tri-FLAG tag has been introduced at this site (e.g. pSANG10-3F, Figure 1b).
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CEO of Professional Science Editing for Scientists @ prosciediting.com