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Fig
ure
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
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