PCR amplification of ribosomal DNA spacer regions of Salmonella enteritidis isolates.

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Date
1997-06-01
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Abstract
Polymerase chain reaction (PCR) was used to amplify ribosomal DNA spacer regions from nine Salmonella enteritidis field isolates. Unique products of 480 and 660 bp were obtained from the isolates. PCR product (480bp) was then cloned into pUC18 vector by blunt end ligation.
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Chaudhuri P, Singh VP, Sharma B. PCR amplification of ribosomal DNA spacer regions of Salmonella enteritidis isolates. Indian Journal of Experimental Biology. 1997 Jun; 35(6): 668-9
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https://imsear.searo.who.int/handle/123456789/63336
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Indian Journal of Experimental Biology