Reaktion #422227

ord-4bb86f3d36404c219fecf74828b3bf26

Reaktionsgleichung

CSCC[C@H](NC=O)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](Cc1ccccc1)C(=O)O
fMLP
COc1cc(-c2ccc(N)c(OC)c2)ccc1N
Dianisidine
O=C([O-])CC(O)(CC(=O)[O-])C(=O)[O-]
citrate
OO
hydrogen peroxide
COc1cc(-c2ccc(N)c(OC)c2)ccc1N
dianisidine
COc1cc(-c2ccc(N)c(OC)c2)ccc1N
Dianisidine
COc1cc(-c2ccc(N)c(OC)c2)ccc1N
o-dianisidine
CC1=CC(=O)c2c(O)cccc2C1=O
Plumbagin

Reaktionsbedingungen

Temperatur
37°CELSIUS
Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    workup.ADDITIONTo the tubes were added 0.5 mL of cells at 37° C.
  2. 2
    Sonstigewas stored at −20° C. for later assay
  3. 3
    Temperaturincrease in absorbance at 450 nm that

Vorschrift

Eppendorf tubes containing either 25 mg of CPPD or 1 uM fMLP (with 0.5 uM cytochalasin B) were maintained at 37° C. To the tubes were added 0.5 mL of cells at 37° C. followed by shaking to initiate the reactions. At appropriate times, tubes were centrifuged at 10,000× g for 10 s and 0.4 mL of supernatant was stored at −20° C. for later assay. Myeloperoxidase (MPO) activity was measured by the increase in absorbance at 450 nm that accompanies the oxidation of o-dianisidine. Dianisidine (7.8 mg) was dissolved in 100 mL of 0.1 M citrate buffer, pH 5.5 and to a 1 mL cuvette were added 0.89 mL of the dianisidine solution, followed by 50 mL of 1% Triton X 100, 10 mL of 0.05% hydrogen peroxide and 50 mL of crystal-cell supernatant. MPO activity was determined from the change in absorbance (450 nm) per minute, (ΔA450), using the following relationship: Dianisidine oxidation (nmol/min)=50 ΔA450

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US08883856B2uspto-grants-2014_11