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Questions related from Miriam Khider
Dear, I am working with a slow growing bacteria. I need to harvest 10 ml at the low OD and approximately 5ml at high OD for RNA isolation and transcriptomics. I saw that most people use RNA...
29 March 2017 581 7 View
I am doing this for the first time and I need a quick check wether i have understood the method correctly. My plasmid has a CAM gene which is going to be deleted and replaced with KAN. 1. Primer...
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I am following some electroporation protocols found in the literature. Using Genepulser X cell from BioRad and cuvettes 0.2 cm (2mm) The V (voltage) in the instrument is from 160V to 2500V How to...
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Can Colony PCR be applied to genomic DNA, or only for ligation (vector/insert) screening?
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For transcriptional fusion do you clone the promoter of interest upstream of the reporter gene which is promoterless to study the promoter strength? And in translational fusion do you clone the...
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I need to use 1 ul of 3-10 ng of my pcr product to sequence by BigDye 3.1 protocol. How can i measure the concentration of my pcr product out of the gel ladder/standard?
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I need help with overlapping PCR, I have 4 primers A, B, C and D where B and C have complementary bases. 1. first PCR run with Phusion Polymerase from Thermo F-530S to generate PCR product AB and...
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