𝜈 | Molecule 1 : 1 Host | ||
Ka = | 1600.0 | ± 160.0 | M-1 |
Kd = | |||
logKa = | |||
T | 25.0 °C | ||
Energy | kJ mol-1 | kcal mol-1 | |||
---|---|---|---|---|---|
ΔG | = | -18.29 | ± 0.25 | -4.37 | ± 0.06 |
Detection Method: | Competitive | |||
Assay Type: | Competitive Binding Assay | |||
Technique: | Fluorescence | |||
𝛌ex | = | 336.0 nm | ||
𝛌em | = | 380.0 nm |
Solvent System | Buffer System | 10 mM ammonium acetate pH-6.0 |
Solvents | water | 100.0 % |
Additives | Ammonium acetate | 10.0 mM |
Source of Concentration | ||
Total concentration | 10.0 mM | |
pH | 6.0 |
Citation: |
A. Hennig, H. Bakirci, W. M. Nau, SupraBank 2024, Label-free continuous enzyme assays with macrocycle-fluorescent dye complexes (dataset). https://doi.org/10.34804/supra.20210928224 |
Link: | https://doi.org/10.34804/supra.20210928224 |
Export: | BibTex | RIS | EndNote |
Citation: |
A. Hennig, H. Bakirci, W. M. Nau, Nat Methods 2007, 4, 629–632. |
Link: | https://doi.org/10.1038/NMETH1064 |
Export: | BibTex | RIS | EndNote | |
The plot depicts the binding isotherm simulation of a 1:1 interaction of D/L-Trp (0.0125 M) and CB7 (0 — 0.025 M).