7 Questions 6 Answers 0 Followers
Questions related from Bahare Khoshkholgh
Hello I am searching for a suitable 16srRNA primer for identifying bacteria in the genus of pseudomonas. I have found many sequences and I dont know which is the best. Can anyone help me what...
06 June 2023 5,900 4 View
I want to know the stationary phase PGPR pseudomonas such as fluorescence pseudomonas. can anyone help me what is the OD of those bacteria in stationary phase?
05 May 2023 9,500 3 View
Hi, Recently, I have done PCR with 16S primer for identifying my bacteria. I have run my control negative with my primers and without DNA. Unfortunately, I saw a band the same size as my pcr...
02 March 2023 6,459 5 View
I want to preserve my bacteria in -80 degree. Whould anyone help me say that What is the best medium to preserve bacteria in the long term? I know lots of medium for saving those, but I want to...
08 October 2022 5,807 3 View
Recently, I bought a King B media culture for detection of flueorscence Pseudomonads, but it's made of acid casein, gelatine peptine, potassium phosphate and Mgso4, instead of proteose peptone and...
09 September 2022 8,385 0 View
Is there any way to return the fluerscence properties of the Pseudomonas bacterial strains? Because this fluerscence properties are quickly distroyed under -80 degree, when they have stocked...
05 September 2022 7,679 4 View
I stored my bacteria in -80 degrees, but bacteria have got weak and didn't grow. why did it happen like that? Is it possible that bacteria have destroyed? what is the best method for the storage...
22 June 2022 3,254 1 View
