Original Article

“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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IssueVol 7 No 1 (2015) QRcode
SectionOriginal Article(s)
Keywords
DNA size marker PCR sequencing Bacillus anthracis Sterne 34F2

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Creative Commons License This work is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License.
How to Cite
1.
Sekhavati M, Tadayon K, Ghaderi R, Banihashemi R, Jabbari AR, Shokri G, Karimnasab N. “In-house” production of DNA size marker from a vaccinal Bacillus anthracis strain. Iran J Microbiol. 2015;7(1):45-49.