Примери за използване на Binding sites на Английски и техните преводи на Български
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There is no saturation of binding sites in the concentration range reached with therapeutic doses.
MIPs in nano-format open promising possibilities for improving the homogeneity of the binding sites.
Saturation of binding sites leads to more free salicylate and increased toxicity.
The labeled antigen competes for primary antibody binding sites with the sample antigen(unlabeled).
Pharmacology Magnesium is a physiological calcium antagonist andis able to displace it from its binding sites.
Saturation of binding sites leads to an increase in the amount of free salicylate and an increase in toxicity.
Each Y-shaped antibody mol ecule has atleast two binding sites that can attach to a specific epitope on an antigen.
When the concentration increased to 45.0 μg/ ml, the binding of clarithromycin decreased to 41%,which may indicate saturation of the binding sites.
Unlike affinity, avidity describes the multivalent binding between multiple binding sites of the ligand and ligate, respectively.
They can also block the binding sites of hormones in the body and interfere with production, degradation or transportation.
A drug, if present in the urine specimen below its cutoff concentration,will not saturate the binding sites of its specific antibody.
There are over 3751 magnesium binding sites in your body- so many because your body requires magnesium for more than 300 biochemical functions.
This indicates minimal risk of drug-drug interactions by displacement from binding sites during concomitant administration of other substances.
The binding sites become partially protonated in the stomach and interact through ionic and hydrogen bonding with both dietary phosphate anions and bile acids in the duodenum.
They can also lead to a blockage of the hormone binding sites in the body, or interfere with hormone degradation, production or transportation.
It is assumed that prolactin increases the absorption of testosterone andcholesterol from the prostate and increases binding sites for dihydrotestosterone(DHT).
Intelligent tools CorelCAD, such as binding sites, the binding sites and guides polar guide, accelerate the development and construction drawings.
Drugs that may be present in the urine specimen compete against their respective drug conjugate for binding sites on their specific antibody.
In in vitro studies, enfuvirtide was not displaced from its binding sites by other medicinal products, nor did enfuvirtide displace other medicinal products from their binding sites.
Drugs which may be present in the specimen being tested by the drug test to compete against their respective drug conjugate for binding sites on their specific antibody.
Activated charcoal is made when charcoal is superheated and all the binding sites of the carbon making up the charcoal are freed, allowing incoming molecules and atoms to bind with them.
Drugs which may be present in buy green sibutramine online the urine specimen compete against their respective drug conjugate for binding sites on their specific antibody.
Your body has specific binding sites, or“locks,” on many of its cell types, and your body produces various endocannabinoids, or“keys,” which bind to those cannabinoid receptors to activate and“unlock” them.
Activated charcoal is useful as a filter, butit is possible for it to adsorb so many contaminants that there are no more binding sites or pores to take in incoming substances.
The human body possesses specific binding sites(“locks”) on the surface of many cell types, and our body produces several endocannabinoids(“keys”) that bind to these cannabinoid receptors(CB) to activate or“unlock” them.
The mean±standard deviation(SD) dissociation constant(Kd) of binding was 5.1± 3.0 ng/ml,denoting the concentration at which 50% of binding sites in blood cells were occupied.
Vinflunine binds to tubulin at or near to the vinca binding sites inhibiting its polymerisation into microtubules, which results in treadmilling suppression, disruption of microtubule dynamic, mitotic arrest and apoptosis.
When this happens, the elements andcompounds bound with the carbon atoms are removed and all the binding sites for carbon are“free” for binding with incoming molecules and atoms.
Radioligand binding studies have demonstrated that granisetron has negligible affinity for other receptor types, including 5HT1, 5HT2, 5HT4 anddopamine D2 binding sites.
The avidity of the antibody depends on the affinities of the individual antibody binding sites, but is greater than the binding affinity as all the antibody-antigen interactions must be broken simultaneously for the antibody to dissociate completely.