genesig Real-Time PCR Detection Kit for Coxiella burnetii (DNA gyrase subunit A), Standard

Kits and Assays / Kits-PCR, genesig™

-20°C

The genesig® Kit for Coxiella burnetii (C. burnetii) genomes is designed for the in vitro quantification of C. burnetii genomes. The kit is designed to have the broadest detection profile possible while remaining specific to the C. burnetii genome.

The primers and probe sequences in this kit have 100% homology with a broad range of C. burnetii sequences based on a comprehensive bioinformatics analysis.

genesig Standard Kit:
Product features:
• Exceptional value for money
• Rapid detection of all clinically relevant subtypes
• Positive copy no. standard curve for quantification
• Highly specific detection profile
• High priming efficiency
• Broad dynamic detection range (>6 logs)
• Sensitive to < 100 copies of target
• Accurate controls to confirm findings

STANDARD KIT COMPONENTS:
• C. burnetii specific primer/probe mix (150 reactions BROWN); FAM labelled
• C. burnetii positive control template (RED); for standard curve
• RNAse/DNAse free water (WHITE); for resuspension of primer/probe mixes
• Template preparation buffer (YELLOW); for resuspension of positive control template and standard curve preparation

KIT STORAGE AND STABILITY:
This kit is stable at room temperature but should be stored at -20°C on arrival. We do not recommend using the kit after the expiry date stated on the pack. Once the lyophilized components have been re-suspended, unnecessary repeated freeze/thawing should be avoided. The kit is stable for six months from the date of resuspension under these circumstances.
If a standard curve dilution series is prepared this can be stored frozen for an extended period. If you see any degradation in this serial dilution a fresh standard curve can be prepared from the positive control.

SUITABLE SAMPLE MATERIAL:
All kinds of sample material suited for PCR amplification can be used. Please ensure the samples are suitable in terms of purity, concentration, and DNA integrity. Always run at least one negative control with the samples. To prepare a negative control, replace the template DNA sample with RNAse/DNAse free water.

DYNAMIC RANGE OF TEST:
Under optimal PCR conditions genesig® C. burnetii detection kits have very high priming efficiencies of >95% and can detect less than 100 copies of target template.

PRODUCT MANUAL:
http://www.genesig.com/assets/files/c_burnetii_std.pdf

INSTRUMENTATION REQUIREMENTS:
Designed for use with real-time PCR instruments. . For use in genesig® q16, look for the “Easy” nomenclature.

ABOUT THE genesig® KITS:
genesig® kits are sold for research use only and are not licensed for diagnostic procedures.

Nucleic acid testing (NAT) is the method of choice for detection and quantification of a wide range of micro organisms. Primerdesign manufactures and supplies high quality quantitative Real-Time PCR kits for the detection and simultaneous quantification of numerous significant pathogens. A copy number standard curve is provided for quantification and an the internal extraction template (DNA or RNA), controls for the quality of the nucleic acid extraction and eliminates false negative results.

The kit is designed with the broadest possible detection profile to ensure that all clinically relevant strains and subtypes are detected. Target sequences are selected by working with data from key opinion leaders in the field. Multiple sequence alignments and unprecedented Real-Time PCR expertise in design and validation ensure the best possible kit. 

Details of the target and priming specificity are included in the individual handbooks above. Packaged, optimized and ready to use.

DNA/RNA EXTRACTION:
genesig® Easy DNA/RNA extraction kits are a simple to use, low cost and powerful extraction technology suitable for virtually all sample types.