Technique / Molecular Biology / Bacterial plasmid bacterial phages vectors
Transformation efficiency
Transformation efficiency
If you are getting low transformation efficiency with chemically competent cells:
There were impurities in the DNA. Remove phenol, protein, detergents, and ethanol, by ethanol precipitation or GlassMAX DNA Isolation Systems. There was excess DNA. Use no more that 1-10 µg of DNA in <5 pl volume/100 pl of cells. (Shanta Dube, Life Technologies, Inc.)
Last update 28-Jun-2002, Rating of 2 votes.
Post your message in Bacterial plasmid bacterial phages vectors forum
Write your comment
|
By amna shah
on 06-Jan-2006
the transformation efficiency is suspiciously TOO HIGH... what could have gone wrong?? |
|
By srinivas reddy
on 21-Jun-2005
iam srinivas a post graduate in bioinformatics(annamalai university,tamilnadu) now iam in searchof job in bioinformatics,so let me vacancies in hyderabad |
|
By rafia.razzaque
on 28-Jun-2002
the ligation reaction is not working |
Please Login or Register to Post
Related resource
PlasMapper Version 1.0 plasmid maps
E. Coli Plasmid Vectors: Methods and Applications (Methods in Molecular Biology)

E.Coli strain database (searchable)

Lambda protocol

E.coli recombinant protein proteolysis

need help for the transformation

Best vector for expressing recombinant antibody fragments?

Protocol for making competent E coli

Promotions