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Questions related from Mohan Amarasiri
I want to construct the whole genome sequence of a bacterium isolated in our lab using the order/move contigs option of MAUVE. I used the reference genome and the program provided me two...
28 June 2016 4,343 1 View
I want to isolate some antigen positive bacteria from an environmental sample and planning to use FACS for the process. As positive and negative controls I have used bacteria which confirmed to be...
22 October 2015 2,656 22 View
I am using molecular probes red bacterial stain in flow cytometry. Can anybody explain how the dead bacterial cells can have higher fluorescence intensity?
10 July 2015 2,275 4 View
I want to detect the presence of bacteria and antigens from the same sample using two fluorescent stains with flow cytometry. How can I double stain the sample for that purpose?
22 April 2015 8,291 6 View
I have extracted some median value and percentile data from publications and I would like to convert them to mean and confidence interval data for a comparison. What are the simple statistical...
20 January 2015 8,879 6 View
I want to store some feces samples for bacteria isolation. I am planning to store them in -800C. Will it be ok? How long can I store that way without destroying the bacteria?
08 December 2014 1,655 4 View
I want to measure polysaccharide concentrations and the size. Can I use western blotting for that purpose?
07 December 2014 8,423 2 View
I am treating bacterial cells with periodate for degrading the glycoproteins. Will it effect the viablility of cells?
29 November 2014 2,478 2 View
I want to do virus concentration measurements and I am planning to store my samples in the -80 C freezer. How long can I keep them without degradation of the bacteria and viruses?
15 January 2014 6,869 0 View
A typical Lipopolysaccharide concentration inside a MBR is required for an experimental design. Are there any typical values which can be assigned for the initial design?
09 January 2014 6,960 1 View