Reaktionsgleichung
[CH3:1][C:2]([C:5]#[C:6]/[CH:7]=[CH:8]/[CH2:9][N:10]([CH2:12][C:13]1[CH:14]=[CH:15][CH:16]=[C:17]2[CH:22]=[CH:21][CH:20]=[CH:19][C:18]=12)[CH3:11])([CH3:4])[CH3:3].Cl>C(=O)([O-])[O-]>[CH3:4][C:2]([C:5]#[C:6]/[CH:7]=[CH:8]/[CH2:9][N:10]([CH2:12][C:13]1[CH:14]=[CH:15][CH:16]=[C:17]2[CH:22]=[CH:21][CH:20]=[CH:19][C:18]=12)[CH3:11])([CH3:1])[CH3:3]Komponenten
Edukt 1
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
Microtiter plates are coated with 5 μg/ml terbinafine hydrochloride—protein (BSA) conjugate in carbonate buffer overnight at 4°, then saturated with blocking reagent [SuperBloc® buffer (Pierce)] and washed 3× with 0.05% (v/v) PBS-TWEEN® (polyoxyethylene 20 sorbitan monoleate). The hybridoma supernatants to be screened are diluted in a 1% (w/v) solution of BSA in PBS-TWEEN® (polyoxyethylene 20 sorbitan monoleate), and incubated for 2 hours at 37°. Level of bound antibody is measured by anti-mouse IgG rabbit immunoglobulin coupled to horseradish peroxidase with OPD as the substrate. After incubation for one hour at room temperature the enzymatic substrate is hydrolyzed and absorbance at 490/650 nm is measured after 15 minutes incubation in the dark.
Aufarbeitung
- washsaturated with blocking reagent [SuperBloc® buffer (Pierce)] and washed 3× with 0.05% (v/v) PBS-TWEEN® (polyoxyethylene 20 sorbitan monoleate)
- additionThe hybridoma supernatants to be screened are diluted in a 1% (w/v) solution of BSA in PBS-TWEEN® (polyoxyethylene 20 sorbitan monoleate)
- waitAfter incubation for one hour at room temperature the enzymatic substrate is hydrolyzed
- waitabsorbance at 490/650 nm is measured after 15 minutes incubation in the dark
Quellen und Nachweise
- ORD-Eintrag
- ord-264059eabc304be78d9bf253c3e9b904
- Quelldatensatz
- uspto-grants-2006_10
- Patentnummer
- US07122184B2
Verknüpfte Notizen
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