G.tigrina Hox gene DthoxC insertion into prokaryote E.coli / (by UNIamCloning)/2011/10/27 - Revision history

Courtney Calhoun: /* New Ampicillin Plates of GFP and ATF1 DNA */

2011-10-27T23:02:07Z

New Ampicillin Plates of GFP and ATF1 DNA

←Older revision		Revision as of 23:02, 27 October 2011
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	==New Ampicillin Plates of GFP and ATF1 DNA==		==New Ampicillin Plates of GFP and ATF1 DNA==
-	* Today in lab we made more plates using the rest of our samples. We used three samples of ATF1 from 2009, three samples of GFP from 2009, two samples each of ATF1 and GFP from 2010, and two samples each of these parts from 2011. Also, a negative control (water and competent cells) was used totaling fifteen ampicillin plates used. It was decided not to make a positive control, a negative control on a non-ampicillin plate, or a sample of competent cells only on a non-ampicillin plate because we already knew from our last trial of control plates that they are still living post-transformation. Each plate was loaded with 200µl of sample and when this process was completed we put all the plates into an oven overnight. Hopefully we will see some growth tomorrow!	+	* Today in lab we made more plates using the rest of our samples. We used three samples of ATF1 from 2009, three samples of GFP from 2009, two samples each of ATF1 and GFP from 2010, and two samples each of these parts from 2011. Also, a negative control (water and competent cells) was used (to make sure the ampicillin plates are working properly) totaling fifteen ampicillin plates used. It was decided not to make a positive control, a negative control on a non-ampicillin plate, or a sample of competent cells only on a non-ampicillin plate because we already knew from our last trial of control plates that they are still living post-transformation. Each plate was loaded with 200µl of sample and when this process was completed we put all the plates into an oven overnight. Hopefully we will see some growth tomorrow!

Courtney Calhoun: /* Entry title */

2011-10-27T22:57:36Z

Entry title

←Older revision		Revision as of 22:57, 27 October 2011
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-	==~~Entry title~~==	+	==New Ampicillin Plates of GFP and ATF1 DNA==
	* Today in lab we made more plates using the rest of our samples. We used three samples of ATF1 from 2009, three samples of GFP from 2009, two samples each of ATF1 and GFP from 2010, and two samples each of these parts from 2011. Also, a negative control (water and competent cells) was used totaling fifteen ampicillin plates used. It was decided not to make a positive control, a negative control on a non-ampicillin plate, or a sample of competent cells only on a non-ampicillin plate because we already knew from our last trial of control plates that they are still living post-transformation. Each plate was loaded with 200µl of sample and when this process was completed we put all the plates into an oven overnight. Hopefully we will see some growth tomorrow!		* Today in lab we made more plates using the rest of our samples. We used three samples of ATF1 from 2009, three samples of GFP from 2009, two samples each of ATF1 and GFP from 2010, and two samples each of these parts from 2011. Also, a negative control (water and competent cells) was used totaling fifteen ampicillin plates used. It was decided not to make a positive control, a negative control on a non-ampicillin plate, or a sample of competent cells only on a non-ampicillin plate because we already knew from our last trial of control plates that they are still living post-transformation. Each plate was loaded with 200µl of sample and when this process was completed we put all the plates into an oven overnight. Hopefully we will see some growth tomorrow!

Courtney Calhoun: /* Entry title */

2011-10-27T22:56:23Z

Entry title

←Older revision		Revision as of 22:56, 27 October 2011
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	==Entry title==		==Entry title==
-	* Today in lab we made more plates using the rest of our samples. We used three samples of ATF1 from 2009, three samples of GFP from 2009, two samples each of ATF1 and GFP from 2010, and two samples each of these parts from 2011. Also, a negative control (water and competent cells) was used totaling fifteen ampicillin plates used. Each plate was loaded with 200µl of sample and when this process was ~~complete~~ we put all the plates into an oven overnight. Hopefully we will see some growth tomorrow!	+	* Today in lab we made more plates using the rest of our samples. We used three samples of ATF1 from 2009, three samples of GFP from 2009, two samples each of ATF1 and GFP from 2010, and two samples each of these parts from 2011. Also, a negative control (water and competent cells) was used totaling fifteen ampicillin plates used. It was decided not to make a positive control, a negative control on a non-ampicillin plate, or a sample of competent cells only on a non-ampicillin plate because we already knew from our last trial of control plates that they are still living post-transformation. Each plate was loaded with 200µl of sample and when this process was completed we put all the plates into an oven overnight. Hopefully we will see some growth tomorrow!

Courtney Calhoun: /* Entry title */

2011-10-27T22:53:17Z

Entry title

←Older revision		Revision as of 22:53, 27 October 2011
Line 7:		Line 7:
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	==Entry title==		==Entry title==
-	* ~~Insert content here~~...	+	* Today in lab we made more plates using the rest of our samples. We used three samples of ATF1 from 2009, three samples of GFP from 2009, two samples each of ATF1 and GFP from 2010, and two samples each of these parts from 2011. Also, a negative control (water and competent cells) was used totaling fifteen ampicillin plates used. Each plate was loaded with 200µl of sample and when this process was complete we put all the plates into an oven overnight. Hopefully we will see some growth tomorrow!

Courtney Calhoun: Autocreate 2011/10/27 Entry for G.tigrina_Hox_gene_DthoxC_insertion_into_prokaryote_E.coli_/_(by_UNIamCloning)

2011-10-27T22:45:31Z

Autocreate 2011/10/27 Entry for G.tigrina_Hox_gene_DthoxC_insertion_into_prokaryote_E.coli_/_(by_UNIamCloning)

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