Cookie Consent by
genekam logo
  • usa
    • german
    • russia
    • china
Duissernstr. 65a · 47058 Duisburg · Germany
Tel. +49 203 / 555 858 -31 / 32 / 33 · Fax: +49 203 / 35 82 99
Latest News:

Genekam to attend BIO CEO & Investor Conference
February 26-27, 2024 | New York

Latest News:

Genekam registered with EUDAMED - A step towards meeting the latest IVDR requirements!

  • LSX World conference

    Genekam is to attend LSX World conference 29-30 April, 2024, Business Design Center, London, UK

  • MEDICA 2024

    Visit us on Medica Duesseldorf, 11.-14. November 2024

Coxiella burnetii

Name of ready to use
Storage DOC Amount Price*
FR002Coxiella burnetii -20°C 100519,-€

Technical Details

FR002 Coxiella burnetii, 100 reactions

Coxiella burnetii is the causative agent of zoonostic disease called Q-fever. It is an obligate intracellular rickettsial micro organisms. It has been found throughout the world except New Zealand. it comes in human beings, farm animals (like cattle, sheep, goat), pet animals like dog, cat, wild animals as well as athropods. Infected animals may not show the symptoms. Therefore it is essential to identify such carriers. In USA, there is very high percentage of milk probes positive for Coxiella burnetii in cattle. Quantitive assays should cover wide range of concentrations since the absolute coxiella load as well as its time course are important diagnostic parameters for indicating the prognosis as well as therapy. Coxiella burnetii has been found in spleen, liver, aborted fetus, lungs, blood etc. Coxiella burnetii can be detected through cell culture methods as well as serological methods like FAT, ELISA etc, but these all methods have one or other following drawbacks: low sensitivity, cross reactions or need a long time for detection, therefore PCR is merging as godstandard as this is highly sensitive and finished within a few hours. With real time PCR, one can get the results within 3-4 hours as there is no post PCR stage. In case one can run the known standards with PCR, it can give you the exact number of copies present in the sample. In case the quantititive standard is not available, one can compare 2 samples as one see the bacterial load as curve during real time assay. Real time curves can be helpful during the therapy and predict the success of the treatment.
In case the load is going down, it means that the therapy is going to be successful, otherwise one has to think about other alternatives.

target gene: highly conserved region of IS gene of coxiella burnetii

Samples: blood, serum, plasma, cell culture, milk, spleen, aborted fetus tissue and other body fluids. Our test can be used to detect Coxiella burnetii in ticks .

Keypoints : It has been checked for cross reactions for related and non related micro organisms like Toxoplasma gondii, Leptospira, Mycoplasma, Neospora caninum, Treponema pallidum, different Babesia, Mycoplasma, negative tick, negative human DNA, negative bird DNA and many more. It has been diluted for serial dilutions. It needs isolated DNA, which can be used through commercial kits as well as home made methods.

Detection limit: minimum : 100 genomes per assay (detection Ct is lower 36 (this should be taken as positive); 36-40 Ct should be taken as weak positive.)

Contents of the kit: Polymerase, buffer, PCR master mix, nucleotides, primers, probes (with 6-carboxyfluoresceine and 6-carboxytetramethylrhodamine), positive control, negative control, molecular water and manual.

Storage: -20 degree

Recommendations: always run the two samples per probe. Species specific internal control can be used.

- only for in vitro use
- for veterinary use
- for human use, only for research use
- to be used through technical person
Coxiella burnetiiCoxiella burnetiiCoxiella burnetii