Figure 1. Agarose Gel electrophoreses (1 %) showing PCR amplification of the ChrT gene: Lane 1, DNA marker; lane 4, PCR amplification of the ChrT gene fragment; a 305bp fragment obtained by PCR amplification with the Scfmn1F and Scfmn1R primers, lane2 and 3, PCR amplification of the complete DNA; the 400bp and 650bp ChrT gene obtained by PCR amplification with the ScfmnF and ScfmnR primers

From

Genetic Characterization of Pseudomonas stutzeri Strain M15-10-3, the Highly Efficient Cr Accumulator Isolated from Leather Tanning Industrial Wastewater

Alawiah Mohammad Alhebshi, Ebtesam El-Bestawy

Journal of Applied & Environmental Microbiology. 2018, 6(3), 67-72 doi:10.12691/jaem-6-3-2