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Questions related from Priyanka Singh
I am facing many technical issues while working with them. Anyone who has worked with them can drop me an email on [email protected]
18 August 2025 2,053 0 View
I have recently started working on quantifying the virulence factor of Pseudomonas aeruginosa. In winters when there was a reducing environment, I was getting a greenish tint in my bacteria. Now...
01 April 2025 744 0 View
Most of the methods in the paper are given for bacterial culture for quantifying QS-associated virulence factors like pyocyanin. What methods can be employed for biofilm setup in microtitre and...
28 March 2025 1,463 1 View
If a particular bacteria's biofilm mature at 48 hr and we are trying to study its disruption using particular treatment . We give the treatment at biofilm maturation i.e 48 hr. And then quantify...
27 March 2025 1,520 3 View
For qualitative analysis of gram-negative bacterial biofilm. What is the ideal stain that we can go with? I have tried CV, it gives good images but not good compared to gram-positive ones. It gets...
13 December 2024 8,374 6 View
As in my previous question i was concernes about the change observed in my culture. it was turning into green color and was slightly watery in nature and usually it is fade yellow and more mucoid...
26 November 2024 3,431 0 View
?whenever winters arrive my bacterial culture turns into green color. i have searched and came to know that p.aeruginosa forms pyocyanin pigment that is green colored. does it will affaect my...
25 November 2024 5,568 2 View
If we are quantifying bacterial biofilm in microtiter plate, we are using heat treatment for fixing step, we have sets of expt. one we have to do today other we have to do tomorrow, does today...
04 October 2024 1,057 0 View
when we grow biofilm in test tube, the pipette often do not reach near the content. so we have to decane it directly or use a smaller test tube.
18 July 2024 3,882 0 View
