Difference between revisions of "Part:BBa I763032:Experience"

Latest revision as of 18:18, 26 October 2007

We first cloned the part inside a high copy number plasmid (pSB1AK3). When we checked part lenght with a gel electrophoresis that was ok. Anyway, when we checked for fluorescence we observed that just some bacteria were fluorescent. We grew bacteria in M9 + lactose + IPTG (2 mM),but always we saw that not all of them were fluorescent.

So, we tried tried the same cloning in a low copy number plasmid (pSB4A3), thinking that it could better with a lower amount of cI repressor, but we obtained the same result.

As expected, we observed that bacteria transformed with BBa I763032 are no fluorescent in LB medium untill they reached the growth stationary phase. When all the glucose was depleted bacteria were fluorescent due to lack in catabolite repression.

Applications of BBa_I763032

User Reviews

UNIQ4d1be108158dfb70-partinfo-00000000-QINU UNIQ4d1be108158dfb70-partinfo-00000001-QINU

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 __NOTOC__
-This experience page is provided so that any user may enter their experience using this part.<BR>Please enter
-how you used this part and how it worked out.
+We first cloned the part inside a high copy number plasmid (pSB1AK3). When we checked part lenght with a gel electrophoresis that was ok. Anyway, when we checked for fluorescence we observed that just some bacteria were fluorescent. We grew bacteria in M9 + lactose + IPTG (2 mM),but always we saw that not all of them were fluorescent.
+So, we tried tried the same cloning in a low copy number plasmid (pSB4A3), thinking that it could better with a lower amount of cI repressor, but we obtained the same result.
+As expected, we observed that bacteria transformed with BBa I763032 are no fluorescent in LB medium untill they reached the growth stationary phase. When all the glucose was depleted bacteria were fluorescent due to lack in catabolite repression.
 ===Applications of BBa_I763032===