M15 transformation problem? - (Sep/18/2005 )
Hello!!!
  I am trying to transform M15 with my construct , which contains my PCR product in PQE30 vector.I conformed presence of my insert by RE. But facing problem in M15 tansformation step.I used PQE30 only as control to check whether my insert is toxic to the bacteria.I do not find any colony there. M15 competent cells grow well in absence of any  antibiotic or in  presence of Kanamycin 25 microgm/ml  concentration. 
  Now i am confident , my insert is not toxic atleast. Either M15 failed to takeup plasmid due to its lost competent factor  or the antibiotic which I used  in plate were  in higher side. Can anyone suggest me how to deal with M15 expression host? Please let me know abt  Incubation time , which media do u use after heat shock ............
     Thanks in advance.
Saikat  Chakraborty
Mie University , Japan
Use electroporation. It is much less sensitive to difference in competency between strains.
Daniel
DNA sequencing
