Neisseria gonorrhoeae Quantitated Bacterial DNA
- 貨號 Cat. No.
- 08-924-000
- 規格 Size
- 250 µl
- 品牌 Brand
- Advanced Biotechnologies Inc
Description
Catalog Number:
08-924-000
Status:
Current product--usually ships within 2 business days
Discount:
Quantity discounts are available for quantities of 5 or more. Please contact us for details.
Size:
250 µL
Use:
For research use only. Not for use in diagnostic procedures.
Storage Temperature:
-20ËšC
Bacteria: Neisseria gonorrhoeae
Bacterial Preparation: Concentrated bacteria from cultures
Suspending Buffer: 10 mM Tris, 1 mM EDTA, pH 8.0
PCR Analysis of DNA Control: PCR analysis was performed on purified Neisseria gonorrhoeae DNA using the PE Biosystems GeneAmp® Gold PCR Reagent Kit and primers specific to the B Protein gene of Neisseria gonorrhoeae. The reaction produced a 391 bp fragment.
DNA Quantitation: DNA copy number is determined by real time PCR 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.
Shipping and Storage:
This product is shipped frozen on dry ice. Store at -20°C upon receipt. Avoid multiple freeze-thaw cycles as product degradation may result.
*Note: Upon thawing, centrifuge the vial for a few seconds to remove residual droplets from the lid.
Safe Handling Recommendations:
This DNA extraction procedure has been shown to eliminate the infectivity of most viruses and bacteria; therefore, this product is not considered biohazardous. However, this product is not specifically tested and should be handled in accordance with Good Laboratory Practices and any applicable local guidelines.
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