Sentence examples for binding concentration from inspiring English sources

Exact(11)

Pres.--I don't know if there is any way for a binding concentration.

The heparin concentration range was varied from 0.2 pM to 216 μM with the optimal binding concentration at 21 nM (the highest charge transfer resistance value).

A similar degree of expansion of the polymeric main chain at the saturated binding concentration of various monovalent salts (LiCl, NaCl, KCl) was observed from measurement of intrinsic viscosity.

F is a vector of any non-linear function of the molecules vectors X = (X1, X2, ‥, Xn), which represents activated concentration levels of signaling molecules (for example through phosphorylation, binding concentration of transcription factors to promoter regions etc).

From the number of ghosts in the assay mixture and the saturation binding concentration corresponding to the best fit to the profile (0.42 (±0.06) µM) we can calculate a copy-number for the receptors on each cell which works out to ∼105.

Data were calculated as c.p.m. and expressed as % binding compared with maximum binding concentration.

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The mean specific D2 ([3H] raclopride) and 5-HT2A ([3H] ketansereceptoreptor binding density of vehicle and THC pretreated groups in various brain regions is shown in Figure 2. THC exposure did not alter D2 or 5-HT2A receptor binding density in any of the brain regions examined, with both THC and vehicle pretreated groups obtaining similar binding concentrations (Figure 2a and b).

Half-maximal binding concentrations were obtained from a 4-parameter binding equation fit to the data.

BoNTB-antibody titer assay showed effective binding concentrations of BoNTB and antibody, as assessed on NativePAGE.

We calculated half-maximal binding concentrations of 76.9 nM, 353 nM, and 188.1 nM for the binding of rBBK32 (21–205) to the 1F3, 1 2F3, and 3F3 respectively, indicating that the MSCRAMM has a high affinity for the immobilized F3 modules.

The binding data for each mAb are displayed in Figure S1 and expressed as half-maximal binding concentrations at equilibrium (K50), which approximate to the equilibrium dissociation constants [58].

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