Examples of using Binding affinity in English and their translations into Danish
{-}
-
Medicine
-
Colloquial
-
Official
-
Financial
-
Ecclesiastic
-
Official/political
-
Computer
Winstrol, another DHT derived drug,also has a binding affinity that is quite low.
Winstrol, andet DHT afledt stof,har også en bindende affinitet, som er ganske lav.In fact, its Relative Binding Affinity is so low that it cannot be effectively measured.
Faktisk, dens relative bindingsaffinitet er så lav, at den ikke effektivt kan måles.Trenbolone substances posses five times the androgen receptor binding affinity of testosterone.
Trenbolon stoffer besidder fem gange androgen receptor bindende forkærlighed af testosteron.This steroid has a binding affinity for androgen receptor that's 5 times the testosterone.
Denne steroid har en bindende affinitet til androgen receptor thats 5 gange testosteron.There is little doubt that this biotransformation contributes at least at some level to the androgenic nature of this steroid,especially when we note that in its initial state Oxymetholone has a notably low binding affinity for the androgen receptor.
Der er næppe tvivl om, at denne biotransformation bidrager i hvert fald på nogle plan til den androgene karakter af dette steroid,især når vi bemærke, at i første medlemsstat Oxymetholone har en særlig lav bindingsaffinitet til androgen receptoren.
Trenbolone has an exceptionally solid binding affinity for the androgen receptor too, also exceeding that of testosterone.
Trenbolon har en utrolig solid bindende forkærlighed for androgen receptor også selv gå videre end testosteron.The binding affinity of 99mTc-depreotide to SSTR was shown in studies of pancreatic tumours in Lewis rats and in vitro in human tumour membranes.
M Tc- depreotids bindings affinitet til SSTR er påvist i studier af pancreastumorer på Lewis rotter og in vitro i humane tumormembraner.Trenbolone has an incredibly strong binding affinity for the androgen receptor too, also going beyond that of testosterone.
Trenbolon har en usædvanlig stærk binding affinitet til androgen receptor så godt, selv gå videre end testosteron.Despite very low binding affinity with the androgen receptor, oxymetholone is highly effective in promoting extensive gains in body mass, mostly by greatly improving protein synthesis.
Uanset ganske lav bindingsaffinitet med androgen receptoren, oxymetholone er meget effektiv i reklame omfattende gevinster i kropsmasse, primært ved væsentligt øge sund proteinsyntese.Interferon beta-1b both decreases the binding affinity and enhances the internalisation and degradation of the interferon-gamma receptor.
Interferon beta- 1b både nedsætter bindingsaffiniteten og øger samtidig internaliseringen og nedbrydningen af inteferon- gamma receptorerne.Despite very low binding affinity with the androgen receptor, oxymetholone is highly effective in promoting extensive gains in body mass, mostly by greatly improving protein synthesis.
Trods meget reduceret binding forkærlighed med androgen receptoren, oxymetholone er meget effektiv i at sikre omfattende gevinster i kropsmasse, for det meste ved høj grad øge sund proteinsyntese.Aripiprazole also exhibited moderate binding affinity for the serotonin reuptake site and no appreciable affinity for muscarinic receptors.
Aripiprazol viser også moderat bindingsaffinitet for serotonin- reuptake site og ingen væsentlig affinitet for muscarine receptorer.Despite really low binding affinity with the androgen receptor, oxymetholone is extremely reliable in promoting comprehensive gains in body mass, primarily by substantially enhancing protein synthesis.
Uanset ganske lav binding forkærlighed med androgenreceptoren, oxymetholon er yderst effektiv til at fremme omfattende gevinster i kropsmasse, hovedsagelig ved i det væsentlige at øge sund proteinsyntese.
In spite of really reduced binding affinity with the androgen receptor, oxymetholone is very efficient in advertising considerable gains in body mass, mainly by significantly boosting healthy protein synthesis.
Trods virkelig lav bindingsaffinitet med androgen receptoren, oxymetholone er meget effektive til at fremme betydelige gevinster i kropsmasse, hovedsagelig ved betydeligt øge sund proteinsyntese.Despite extremely reduced binding affinity with the androgen receptor, oxymetholone is highly reliable in ensuring considerable gains in body mass, mostly by greatly improving healthy protein synthesis.
På trods af ekstremt reduceret binding affinitet med androgen receptoren, oxymetholone er yderst effektiv i at sikre betydelige gevinster i kropsmasse, hovedsagelig ved betydeligt øge sund proteinsyntese.Regardless of very low binding affinity with the androgen receptor, oxymetholone is highly efficient in advertising considerable gains in body mass, primarily by significantly enhancing healthy protein synthesis.
Trods meget reduceret binding forkærlighed med androgen receptoren, oxymetholone er meget effektiv i at sikre omfattende gevinster i kropsmasse, for det meste ved høj grad øge sund proteinsyntese.In spite of really reduced binding affinity with the androgen receptor, oxymetholone is very efficient in advertising considerable gains in body mass, mainly by significantly boosting healthy protein synthesis.
På trods af meget reduceret binding forkærlighed med androgen receptoren, oxymetholone er meget pålidelig i at fremme omfattende gevinster i kropsmasse, hovedsagelig ved en væsentlig styrkelse proteinsyntese.Aripiprazole exhibited high binding affinity in vitro for dopamine D2 and D3, serotonin 5HT1a and 5HT2a receptors and moderate affinity for dopamine D4, serotonin 5HT2c and 5HT7, alpha-1 adrenergic and histamine H1 receptors.
Aripiprazol har høj bindingsaffinitet in vitro for dopamin D2- og D3-, serotonin 5- HT1a- og 5- HT2a- receptorer og moderat affinitet for dopamin D4-, serotonin 5- HT2c- og 5- HT7-, alfa 1- adrenerge og histamin H1- receptorer.The information in this section is based on binding affinity between sugammadex and other medicinal products, non-clinical experiments and simulations using a model taking into account the pharmacodynamic effect of neuromuscular blocking agents and the pharmacokinetic interaction between neuromuscular blocking agents and sugammadex.
Informationen i dette afsnit er baseret på bindingsaffinitet mellem sugammadex og andre lægemidler, ikke- kliniske eksperimenter og simuleringer, hvor der anvendes en model, der tager højde for den farmokodynamiske effekt af neuromuskulære blokkere og den farmakokinetiske interaktion mellem neuromuskulære blokkere og sugammadex.Raloxifene'biological actions, like those of oestrogen, are mediated through high affinity binding to s oestrogen receptors and regulation of gene expression.
De biologiske virkninger af raloxifen er ligesom for østrogen medieret gennem binding med høj affinitet til østrogen- receptorer samt regulering af genekspression.In vitro the affinity binding of recombinant hLH to the LH/ CG receptor on Leydig tumour cells(MA-10) is between that for hCG and that of pituitary hLH, but within the same order of magnitude.
In vitro binder rekombinant hLH til LH/ hCG receptoren på de Leydigske tumorceller(MA- 10) med en affinitet som ligger mellem den som gælder for hCG og hypofysært hLH, men i samme størrelsesorden.The affinity of binding to serum SHBG is relatively high and the SHBG bound fraction is regarded as not contributing to biological activity.
From affinity binding and elution, IEX chromatography, size exclusion, virus inactivation and virus removal, VWR's portfolio of buffers and inorganic salts meet the quality and performance required to maintain protein attributes.
Fra bindingsaffinitet og eluering, IEX-kromatografi og størrelseseksklusion til virusinaktivering og -fjernelse opfylder VWR's portefølje af buffere og uorganiske salte de krav til kvalitet og ydeevne, der er nødvendige for at opretholde proteinets egenskaber.
