“In-house” production of DNA size marker from a vaccinal Bacillus anthracis strain
Abstract
Background and Objectives: DNA molecular weight marker is widely used in molecular biology experiments incurring considerable costs on low-budget settings.
Materials and Methods: Here a PCR-supported procedure is described that uses 10 primer pairs targeting chromosomal DNA from the harmless vaccinal Bacillus anthracis Sterne 34F2 strain as template. A single PCR protocol is used to reproduce all the 10 fragments of a 100 bp DNA size marker.
Results and Conclusion: The unpurified amalgam of 10 PCR products can be directly loaded to agarose gels. This work was intended to develop a reasonably cost-effective DNA ladder that is useful for researchers in laboratories with limited funding.
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Issue | Vol 7 No 1 (2015) | |
Section | Original Article(s) | |
Keywords | ||
DNA size marker PCR sequencing Bacillus anthracis Sterne 34F2 |
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