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European community FP7

(24.01.2014)
Genekam Biotechnology AG has been selected for business mission trip to Tokyo, 26-30 May 2014 under EU GATEWAY TO JAPAN-Healthcare and Medical technologies. Genekam Biotechnology AG is one of 40 companies selected across the European Union.

(13.06.2012)
Genekam got one project for development of Nanoassays for nanomedicine under program ZIM
GENEKAM Biotechnology AG from German Federal Ministry of Economics and Technology.

(02.01.2012)
Genekam is to take part in European Community FP7 ... read more...

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ArabLab The Expo 2014

Visit us in Dubai, UAE from 17.03 to 20.03.2014
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26. CHINA MED 2014

Visit us in Beijing / VR China 21.03. - 23.03.2014
chinamed.net.cn

Medica Düsseldorf 2014

Visit us on Medica 2014 in Düsseldorf from 12.11 to 15.11.2014
medica.de

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New Catalog 2014

Our new Catalog is now released, please download klick here

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Hard fact - is it a sign of quality and confidence in our product?

... in 2004 we had clients in 5 countries in whole year and in 2009 we served 60 countries of the world? There is a surge of medical publications where Genekam PCR Kits are being used. Is it not a sign of quality and trust ?
read more...

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Real time PCR Kits for Influenza A and swine flu (H1N1) (click here to see more information) read more...

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In vitro immunisation of human b-lymphocytes and human monoclonal antibodies read more...

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Genekam Solutions for combating SARS viruses read more...

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Genekam 3D-Stemcell-Solutions read more...

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Genekam 解决方案对抗SARS病毒 read more...

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Genekam-Barcode: Biotech for nature and endangered species
(A new DNA-Test to know the exact species of an animal) read more...

Technical details for realtime PCR kit Chlamydia pneumoniae



FR003 Chlamydia pneumoniae, 100 reactions

Chlaymdia pneumoniae is known to cause the respiratory as well as reproductive diseases in human beings and its role is cardiovascular diseases like atherosclerosis, myocarditits is being discussed in many publications in the near past. Chlamydiae can be detected through staining methods, cell culture methods as well as serological methods like FAT, CFT 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 chlamydia load as curve during real time assay. This micro organism has been detected in animals and there is a need of more research for the role of this bacteria in animals. Real time PCR can be used during the course of treatment as well as to see the pharmokinetics of the drug in vitro against the Chlamydia pneumoniae. During the treatment, if the bacteria load is not going down, it is the indication of the change of line of treatment.

target gene: highly conserved gene of Chlaymdia pneumoniae

Samples: blood, respiratory swabs, serum, genital swabs, heart and related blood vessel samples, tissue and other body fluids.It needs the isolated DNA, which can be isolated through commercial kits or home made methods.

Validation: It has been checked for cross reactions for related and non related micro organisms like Chlaymdia trachomatis, Chlaymdia psittaci, Epstein Barr virus, Staphylococcus aerus, Mycoplasma pneumoniae, uninfected human DNA, Mycoplasma hominis, Legionella and many more. It has been checked for serial dilutions of Chlamydia pneumoniae.

Detection limit: minimum 50 copies per assay (detectio 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, positive control, negative control, molecular water and manual.

Storage: -20 degree

- only for in vitro use
- only for research use
- to be used through technical person



manual

Last modified:
2012-04-05 12:46:27