Sentence examples for binding of fish from inspiring English sources

These observed differences may partially be explained by the binding of FISH probes to non-target microbial groups within complex environmental samples.

Biases and technical limitations of both FISH and pyrosequencing, such as the binding of FISH probes to non-target microbial groups and lack of classification of sequences for defined taxonomic groups from pyrosequencing, may partially explain some differences between the two methods.

Therefore, if the binding of teleost fish CLIP-equivalent fragments to classical class II molecules is not so strong, the fragments may dissociate without help of a DM-equivalent.

Fig. 5A shows the binding of Antarctic fish β-actin to the open conformation of G. gibberifrons CCT (hatched bars) vs the binding the bovine cardiac actin to bovine CCT (black bars); Fig. 5B presents comparable analyses with homologous tubulins as the CPs.

Such data are in agreement with the recent finding that stPrP is not detectable in the intestine of Rainbow trout [ 15], which renders unlikely an active uptake of exogenous PrPSc, but does not exclude an unspecific binding of PrPSc to the fish intestinal mucosa.

These results indicate that scrapie 139A, and possibly BSE, is quickly removed from fish tissues despite evidence of a prion like protein in fish and of a specific binding of PrPSc to the mucosal side of fish intestine.

TTR, however, is generally not the dominant TH transport protein in fish, and binding of PBDEs to thyroxin-binding protein and serum albumin has yet to be examined.

The adaptive mucosal immune system seems to be an important defence mechanism for fish, but the binding of immunoglobulin M (IgM) in mucosal organs has yet to be clarified in fish.

This was demonstrated by their ability to inhibit binding of 17 beta-estradiol to the fish estrogen receptor.

Most sequences of fish skin mucus lectins contain all residues required for binding of two Ca2+ ions near the carbohydrate-binding site (Figure 2), similarly to other lectins.

Fluorescence in situ hybridization (FISH), based on specific binding of fluorescence-labeled oligonucleotide probes, provides a less expensive molecular bridging technique.