Team:TU Darmstadt/Labjournal/Transport
From 2012.igem.org
(Difference between revisions)
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* First [https://2012.igem.org/Team:TU_Darmstadt/Protocols/Colony_PCR colony PCR] of ''Comamonas testosteroni'' for isolation of the following genes: [http://partsregistry.org/wiki/index.php?title=Part:BBa_K808004 tctA 505aa] (1), [http://partsregistry.org/wiki/index.php?title=Part:BBa_K808005 tctB 197aa] (2), [http://partsregistry.org/wiki/index.php?title=Part:BBa_K808002 tctA_503aa] (3), [http://partsregistry.org/wiki/index.php?title=Part:BBa_K808003 tctB 162aa] (4), [http://partsregistry.org/wiki/index.php?title=Part:BBa_K808001 tphC 322aa] (5), 50µl reaction mixture each; analysis of [http://en.wikipedia.org/wiki/Polymerase_chain_reaction PCR] products by [https://2012.igem.org/Team:TU_Darmstadt/Protocols/Agarose_gel_electrohporesis agarose gel electrohporesis] | * First [https://2012.igem.org/Team:TU_Darmstadt/Protocols/Colony_PCR colony PCR] of ''Comamonas testosteroni'' for isolation of the following genes: [http://partsregistry.org/wiki/index.php?title=Part:BBa_K808004 tctA 505aa] (1), [http://partsregistry.org/wiki/index.php?title=Part:BBa_K808005 tctB 197aa] (2), [http://partsregistry.org/wiki/index.php?title=Part:BBa_K808002 tctA_503aa] (3), [http://partsregistry.org/wiki/index.php?title=Part:BBa_K808003 tctB 162aa] (4), [http://partsregistry.org/wiki/index.php?title=Part:BBa_K808001 tphC 322aa] (5), 50µl reaction mixture each; analysis of [http://en.wikipedia.org/wiki/Polymerase_chain_reaction PCR] products by [https://2012.igem.org/Team:TU_Darmstadt/Protocols/Agarose_gel_electrohporesis agarose gel electrohporesis] | ||
:https://static.igem.org/mediawiki/2012/1/15/W1_1_kolo_pcr.png | :https://static.igem.org/mediawiki/2012/1/15/W1_1_kolo_pcr.png | ||
+ | * PCR product purification using the Promega-Kit | ||
+ | * Nanodrop measurements of the purified PCR products: | ||
+ | :(1) : 19.5 ng/µl 260/280=1.58 | ||
+ | :(2) : 61.9 ng/µl 260/280=1.75 | ||
+ | :(3) : 75.1 ng/µl 260/280=1.75 | ||
+ | :(4) : 93.3 ng/µl 260/280=1.85 | ||
+ | :(5) : 91.3 ng/µl 260/280=1.58 | ||
+ | * [ https://2012.igem.org/Team:TU_Darmstadt/Protocols/Restriction_digest Digestion] of PCR products by the restriction enzymes SpeI and EcoRI, heat inactivation after digestion | ||
+ | * Analysis of restriction digest by [https://2012.igem.org/Team:TU_Darmstadt/Protocols/Agarose_gel_electrohporesis Agarose gel electrohporesis] | ||
+ | :https://static.igem.org/mediawiki/2012/1/15/w1_2_restriktionsverdau_s8.png | ||
+ | * Purification of the bands gained form gel electrophoresis (Promega-Kit) | ||
+ | * Nanodrop measurements of the purified products: | ||
+ | :(1) : 8.3 ng/µl 260/280=1.94 | ||
+ | :(2) : 8.9 ng/µl 260/280=1.80 | ||
+ | :(3) : 13.0 ng/µl 260/280=1.57 | ||
+ | :(4) : 1.5 ng/µl 260/280=3.08 | ||
+ | :(5) : 3.7 ng/µl 260/280=2.26 | ||
+ | |||
+ | ===week 2 (28.05.-01.06.12)=== | ||
+ | * Purified products from 1. week were [https://2012.igem.org/Team:TU_Darmstadt/Protocols/DNA_Ligation ligated] into pSB1A2 and subsequently [https://2012.igem.org/Team:TU_Darmstadt/Protocols/Bacterial_transformation transformed] into DH5α (in spite of low concentration) |
Revision as of 21:04, 8 September 2012
Transport
Week 1 (21.-25.05.12)
- First colony PCR of Comamonas testosteroni for isolation of the following genes: [http://partsregistry.org/wiki/index.php?title=Part:BBa_K808004 tctA 505aa] (1), [http://partsregistry.org/wiki/index.php?title=Part:BBa_K808005 tctB 197aa] (2), [http://partsregistry.org/wiki/index.php?title=Part:BBa_K808002 tctA_503aa] (3), [http://partsregistry.org/wiki/index.php?title=Part:BBa_K808003 tctB 162aa] (4), [http://partsregistry.org/wiki/index.php?title=Part:BBa_K808001 tphC 322aa] (5), 50µl reaction mixture each; analysis of [http://en.wikipedia.org/wiki/Polymerase_chain_reaction PCR] products by agarose gel electrohporesis
- PCR product purification using the Promega-Kit
- Nanodrop measurements of the purified PCR products:
- (1) : 19.5 ng/µl 260/280=1.58
- (2) : 61.9 ng/µl 260/280=1.75
- (3) : 75.1 ng/µl 260/280=1.75
- (4) : 93.3 ng/µl 260/280=1.85
- (5) : 91.3 ng/µl 260/280=1.58
- [ https://2012.igem.org/Team:TU_Darmstadt/Protocols/Restriction_digest Digestion] of PCR products by the restriction enzymes SpeI and EcoRI, heat inactivation after digestion
- Analysis of restriction digest by Agarose gel electrohporesis
- Purification of the bands gained form gel electrophoresis (Promega-Kit)
- Nanodrop measurements of the purified products:
- (1) : 8.3 ng/µl 260/280=1.94
- (2) : 8.9 ng/µl 260/280=1.80
- (3) : 13.0 ng/µl 260/280=1.57
- (4) : 1.5 ng/µl 260/280=3.08
- (5) : 3.7 ng/µl 260/280=2.26
week 2 (28.05.-01.06.12)
- Purified products from 1. week were ligated into pSB1A2 and subsequently transformed into DH5α (in spite of low concentration)