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Team:Technion/22 September 2012
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-I ran the PCR products on gel and got several positive results and several negative ones. I got enough positive <br> | -I ran the PCR products on gel and got several positive results and several negative ones. I got enough positive <br> | ||
results for every polymerase type. The required band was 2919 bp. <br> | results for every polymerase type. The required band was 2919 bp. <br> | ||
| + | <gallery perrow="4" widths=150px heights=150px style="color: black; border: 5px ridge #A7A3BF; font: 13px david; background: azure"> | ||
| + | Image:22.9_prefix+RS+polymerase+suffix_test_gel_up-view.jpg | ||
| + | </gallery> | ||
| + | -I have desided to continue to restriction with the following products: K1F-2, N4-1,N4-2, T7-1, T7-2, T3-3, T3-4.<br> | ||
| + | -I cleaned the selected products and got a very high concetration (244-954 ng/ul).<br> | ||
| + | -I cut the selected products with EcoRI and PstI restriction enzymes.<br> | ||
| + | -I cleaned the products and got lower concentration (22-108 ng/ul).<br> | ||
| + | -I ligated the different products to Psb1c3 plasmid that had been cut previewsly with EcoRI and PstI and afterwards <br> went to SIP reaction by Rachel. I didn't have left enough plasmid for the negative control.<br> | ||
| + | -I transformed the lygated Psb1c3 and RS+poly to Top10 E.coli strain.<br> | ||
| + | -I went to sleep. | ||
Revision as of 15:18, 26 September 2012
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Ilya
- Wiki, wiki, wiki...
Inbal
Asaf
-I have made glycerol stocks of all my starters (the selected clones from my long RS+polymerases transformed bacteria).
-I minipreped the starters and got very high concentrations.
-I did a PCR reaction for all the minipreped parts to add prefix and suffix to just the RS+different polymerase
(I have cut the rest of puc19 remeains from the insert).The PCR progrem was for Tm of 56,56.7,57.7 C
-I ran the PCR products on gel and got several positive results and several negative ones. I got enough positive
results for every polymerase type. The required band was 2919 bp.
 |
-I have desided to continue to restriction with the following products: K1F-2, N4-1,N4-2, T7-1, T7-2, T3-3, T3-4.
-I cleaned the selected products and got a very high concetration (244-954 ng/ul).
-I cut the selected products with EcoRI and PstI restriction enzymes.
-I cleaned the products and got lower concentration (22-108 ng/ul).
-I ligated the different products to Psb1c3 plasmid that had been cut previewsly with EcoRI and PstI and afterwards
went to SIP reaction by Rachel. I didn't have left enough plasmid for the negative control.
-I transformed the lygated Psb1c3 and RS+poly to Top10 E.coli strain.
-I went to sleep.
Hila
- Colony PCR for positive clones from the transformation.
Unfortunately no positive clones yet to be found…
- Gel purification for all fragments with 100bp fragments overlap.
