Neisseria gonorrhoeae Heat-Inactivated Cells
Bacterial Preparation: 48 hours growth of N. gonorrhoeae on Chocolate Agar plates was suspended in DPBS and the cell numbers enumerated by spectrophotometry (A550)1
Cell Density: Varies by lot
Suspending Buffer: Dulbecco’s Phosphate Buffered Saline (DPBS), pH 7.4 + 10% Glycerol
ID Tests: Gram stain: Gram negative Diplococci; Oxidase test: Positive; Catalase test: Positive
Enumeration of Cell Numbers: 48 hours growth of N. gonorrhoeae on Chocolate Agar plates was suspended in DPBS and the cell numbers enumerated by spectrophotometry (A550)2
Heat Inactivation: Cells of N. gonorrhoeae suspended in DPBS (2.75 × 108 cells/ml) were inactivated by heat at an optimum temperature and exposure time.
DNA Extraction/Quantitation: Genomic DNA was prepared from bacterial cells using the QIAamp DNA Mini Kit. Bacterial DNA copy number is determined by real time PCR using the Roche LightCycler®. DNA copy number may vary depending on the quantitation method used.
Quantitative DNA PCR Analysis: [Varies by lot]copies/mL
- 1. Hanahan, D. J. Mol. Biol., 166 : 557–580, 1983.
- 2. Hanahan, D. J. Mol. Biol., 166 : 557–580, 1983.


