Mycoplasma pneumoniae Quantitated DNA
Mycoplasma pneumoniae quantitated DNA PCR control.
Mycoplasma: Mycoplasma pneumoniae
Mycoplasma Preparation: Concentrated whole cells of Mycoplasma from broth cultures.
Suspending Buffer: 10 mM Tris, 1 mM EDTA, pH 8.0
PCR Analysis of DNA Control: PCR analysis was performed on purified Mycoplasma pneumoniae DNA using the PE Biosystems GeneAmp® Gold PCR Reagent Kit and primers specific to the P1 cytoadhesin gene of Mycoplasma pneumoniae. The reaction produced a 466 bp fragment.
DNA Copy Number: 1-2 × 104 copies/µL (varies by lot, please contact ABI for details)
DNA Quantitation: Viral DNA copy number is determined by real time PCR1,2 using the Roche LightCycler®. DNA copy number may vary depending on the quantitation method used.
Application: ABI’s quantitated DNA controls are prepared from virus, bacteria, parasites, or mollicutes, and are intended for use as positive PCR quantitation standards for the organism in question. Due to the nature of these products, ABI cannot guarantee their suitability as extraction controls. Additionally, due to the extreme sensitivity of detection in PCR reaction, and since no method of purification can guarantee the complete absence of extraneous agents, DNA controls are not intended for use as negative controls for other organisms.
- 1. "Phenotypic and Genotypic Characterization of Mycobacterium africanum Isolates from West Africa." J. Clin. Microbiol.. 1999;37:1921-1926.
- 2. "Mycoplasma pneumoniae and Its Role as a Human Pathogen." Clinical Microbiology Reviews. 2004;17(4):697-728.
*Note: Upon thawing, centrifuge the vial for a few seconds to remove residual droplets from the lid.



