Zobrazeno 1 - 10
of 17
pro vyhledávání: '"Rong Fu Wang"'
Publikováno v:
Molecular and Cellular Probes. 17:313-317
Guillain–Barre Syndrome (GBS) is a neuromuscular disorder and campylobacteriosis is known to trigger the onset of the disorder. A polymerase chain reaction (PCR) protocol was developed that could specifically amplify a 497-bp region of the UDP-gala
Publikováno v:
Molecular and Cellular Probes. 16:341-350
A membrane-array method was developed for the detection of human intestinal bacteria in fecal samples without using the expensive microarray-arrayer and laser-scanner. The 16S rDNA sequences of 20 predominant human intestinal bacterial species were u
Publikováno v:
FEMS Microbiology Letters. 169:397-402
The fungus, Cunninghamella elegans has been widely used in bioremediation and microbial models of mammalian studies in many laboratories. Using the polymerase chain reaction to randomly amplify the insert directly from the single non-blue plaques of
Publikováno v:
Molecular and Cellular Probes. 12:249-254
A bacterial strain isolated from aquaculture pond slurry, which was extremely sensitive to erythromycin, was used to detect erythromycin at levels as low as 0.05 micrograms ml-1 in aquaculture water, sediments and soil samples. Identification of the
Publikováno v:
Molecular and Cellular Probes. 11:259-265
Polymerase chain reaction (PCR) procedures for Ruminococcus spp. were developed and used for the detection of Ruminococcus spp. in human and animal faeces. The PCR specificity was established for Ruminococcus albus, R. bromii, R. obeum, R. callidus a
Publikováno v:
Environmental Science & Technology. 30:307-311
Polymerase chain reaction (PCR) methods based on the 16S rRNA genes of Mycobacterium sp. PYR-1 and Mycobacterium sp. PAH135, known PAH-degrading bacteria, were developed. An efficient mycobacterial cell lysis procedure was used for the PCR assay. The
Autor:
Rong-Fu Wang, Carl E. Cerniglia, Wei-Wen Cao, Latrina Hairston, Warren L. Campbell, Wirt Franklin
Publikováno v:
FEMS Microbiology Letters. 124:229-237
Six PCR primer sets complementary to the 16S rDNAs (rRNA genes) were developed and shown to be specific for the following anaerobic bacteria: Clostridium clostridiiforme, C. perfringens, C. leptum, Bacteroides vulgatus, B. distasonis, and B. thetaiot
Publikováno v:
Molecular and Cellular Probes. 7:459-463
A polymerase chain reaction (PCR) method specific for Mycoplasma gallisepticum (MG) was evaluated. The PCR method was found to detect as few as two colour changing units (CCU) of MG and did not give false positive reactions with other avian mycoplasm
Publikováno v:
FEMS Microbiology Letters. 106:85-92
A 16S rRNA-based DNA probe and polymerase chain reaction (PCR) method was developed for identification and rapid detection of Listeria ivanovii. The probe (R-1) is 5'-GTAGTGACGCATGTCATCAC-3' corresponding to positions 185-204 in the L. ivanovii 16S r
Publikováno v:
Journal of Rapid Methods and Automation in Microbiology. 1:101-108
A rapid polymerase chain reaction (PCR) method was developed for detection of low numbers of Campylobacter jejuni. In this method, PCR was run directly from lysed C. jejuni cells and used a short denaturing and annealing time, a rapid transition, and