Andere Kunden interessierten sich auch für
![Mycobacterial adenitis in Arusha, Tanzania:]( "Mycobacterial adenitis in Arusha, Tanzania:")
Mycobacterial adenitis in Arusha, Tanzania:38,99 €![Paramedic Rapid Sequence Intubation]( "Paramedic Rapid Sequence Intubation")
Paramedic Rapid Sequence Intubation51,99 €![Identification and characterization of antigens of Malarial parasites]( "Identification and characterization of antigens of Malarial parasites")
Identification and characterization of antigens of Malarial parasites38,99 €![The Biology and Identification of the Coccidia (Apicomplexa) of Marsupials of the World]( "The Biology and Identification of the Coccidia (Apicomplexa) of Marsupials of the World")
The Biology and Identification of the Coccidia (Apicomplexa) of Marsupials of the World54,99 €![National Institute of Parasitic Diseases, China]( "National Institute of Parasitic Diseases, China")
National Institute of Parasitic Diseases, China121,99 €![Duplex RT-PCR Assays For Rapid Detection,sorting Of Influenza Viruses]( "Duplex RT-PCR Assays For Rapid Detection,sorting Of Influenza Viruses")
Duplex RT-PCR Assays For Rapid Detection,sorting Of Influenza Viruses32,99 €![Rapid Diagnosis of Cryptococcal Meningitis]( "Rapid Diagnosis of Cryptococcal Meningitis")
Rapid Diagnosis of Cryptococcal Meningitis23,99 €
Tuberculosis is devastating disease at global level. TB is caused by members of Mycobaterium tuberculosis complex group. Presently available biochemical methods of diagnosis of tuberculosis are not accurate. The highly sensitive polymerase chain reaction (PCR) and specific molecular probes techniques are major advances in early diagnosis and molecular epidemiology of various diseases including TB. It is established that the ribosomal gene region of both the prokaryotic and eukaryotic comprise of sequences that are conserved during evolution interspersed with sequence which are divergent. The analysis of the 16S rRNA gene promoter region for rapid and accurate differentiation and identification of Mycobacterial species and understanding of their phylogenetic relationships is likely to prove to be advantageous over the use of previously used target genes. The resulting sensitivity is likely to allow the generation of RFLP patterns in a matter of hours to differentiate not only between the species investigated in the present study but others as well, by possible detection of novel RFLP patterns. For unidentified cases, PCR product could be characterized by subsequent sequencing.