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Once internalized, for example, GPCRs may be sorted via endosomes and either degraded by transportation to lysosomes or "regenerated" by ligand dissociation/receptor dephosphorylation and recycled to the plasma membrane via recycling endosomes.
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PI−EpCAMhighCD49flow (luminal progenitors) or PI−EpCAMlowCD49bright (bipotent progenitors) cells were sorted via fluorescence-activated cell sorting (FACS).
It has been well-described that proteins tethered to the cell surface by means of a GPI anchor undergo this sort of post-translational modification in the ER before being sorted via the secretory pathway to their final destination, i.e., the plasma membrane.
The resulting spectra were sorted via cosine similarity (normalized dot product), again with 10 ppm mass accuracy.
Reads were sorted via barcode with SFF software (Roche Applied Science, Indianapolis, IN).
Lipoproteins are bound to membrane via a fatty-acyl group linked to a conserved cysteine and are sorted via the Lol system to the inner or outer membranes based on the identity of the amino acid following the cysteine [29], [30].
Pex3 is sorted via a subdomain of the ER to peroxisomes.
All time courses of red/green ratios for all ESTs were sorted via self-organizing maps with Euclidian distance [ 21, 22] (25 cluster (5 × 5) neuron map).
During the protein translation in animals, proteins can enter the classical secretory pathway (SP) in which the protein is sorted via endoplasmic reticulum (ER), e.g., to the Golgi apparatus, plasma membrane, lysosome or to the extracellular matrix.
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