Team:UNIPV-Pavia/Calendar/October/settimana1
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==October, 4th== | ==October, 4th== | ||
- | ON PCR run | + | ON PCR run and than gel run. |
[[Image:UNIPV10_04_10_10_I74_massive_PCR.jpg|thumb|200px|center|I74 massive PCR screening.]] | [[Image:UNIPV10_04_10_10_I74_massive_PCR.jpg|thumb|200px|center|I74 massive PCR screening.]] | ||
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*I77 | *I77 | ||
They were plated on LB+Amp agar plates and let grow ON at +37°C, 220 rpm. | They were plated on LB+Amp agar plates and let grow ON at +37°C, 220 rpm. | ||
+ | |||
+ | |||
+ | ---- | ||
+ | |||
+ | |||
+ | <font color='red' size='+2'>We are now moving all our parts to <partinfo>pSB1C3</partinfo> plasmid</font> | ||
<div align="right"><small>[[#indice|^top]]</small></div> | <div align="right"><small>[[#indice|^top]]</small></div> | ||
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---- | ---- | ||
- | + | <font color='red' size='+2'>We are now moving all our parts to <partinfo>pSB1C3</partinfo> plasmid</font> | |
<div align="right"><small>[[#indice|^top]]</small></div> | <div align="right"><small>[[#indice|^top]]</small></div> | ||
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---- | ---- | ||
- | Transformation of available ligations I75 and I77 (1ul) into ''E. coli'' TOP10. They were plated on LB+Amp agar plates and let grow ON at +37°C, 220 rpm. | + | Transformation of available ligations I75 and I77 (1ul) into ''E. coli'' TOP10, I79 into ''E. coli'' STBL3. They were plated on LB+Amp agar plates and let grow ON at +37°C, 220 rpm. |
---- | ---- | ||
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---- | ---- | ||
- | PCR | + | Colony PCR screening for I78 (eleven colonies were picked from LB+Cm agar plate and were inoculated into 5 ml LB+Cm34 and let grow ON for stock). |
PCR was performed this day but it would have been run the following one (too late this evening). | PCR was performed this day but it would have been run the following one (too late this evening). | ||
+ | |||
+ | ---- | ||
+ | <font color='red' size='+2'>We are now moving all our parts to <partinfo>pSB1C3</partinfo> plasmid</font> | ||
<div align="right"><small>[[#indice|^top]]</small></div> | <div align="right"><small>[[#indice|^top]]</small></div> | ||
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==October, 7th== | ==October, 7th== | ||
I78 screening gel run | I78 screening gel run | ||
- | [[Image:UNIPV10_07_10_10_PCR_I78.jpg|thumb|200px|center|Screening PCR for I78.]] | + | [[Image:UNIPV10_07_10_10_PCR_I78.jpg|thumb|200px|center|Screening PCR for I78 (we cat blank from this picture but it was very clear, trust me).]] |
We had extraband in all samples (similar result in I74 PCR: after digest we had a confirmation that it was right. Probably here it was the same problem: very similar repeated sequences give strange PCR; however we sent it sequencing). | We had extraband in all samples (similar result in I74 PCR: after digest we had a confirmation that it was right. Probably here it was the same problem: very similar repeated sequences give strange PCR; however we sent it sequencing). | ||
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[[Image:UNIPV10_07_10_10_PCR_I79.jpg|thumb|200px|center|Screening PCR for I79.]] | [[Image:UNIPV10_07_10_10_PCR_I79.jpg|thumb|200px|center|Screening PCR for I79.]] | ||
- | + | Same as the previous PCR. We took I79-2 that was inoculated into LB+Cm34 and let grow ON at +37°C, 220 rpm. | |
---- | ---- | ||
Transformation (1ul) of | Transformation (1ul) of | ||
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*I12_1C3 | *I12_1C3 | ||
*I76 | *I76 | ||
- | into ''E. coli'' DH5-alpha | + | into ''E. coli'' DH5-alpha. |
- | They were plated on LB+Cm34 agar plates and let grow ON at +37°C. | + | |
+ | They were plated on LB+Cm34 agar plates (except for I76 that was plated on LB+Amp agar plate) and let grow ON at +37°C. | ||
---- | ---- | ||
- | + | <font color='red' size='+2'>We are now moving all our parts to <partinfo>pSB1C3</partinfo> plasmid</font> | |
<div align="right"><small>[[#indice|^top]]</small></div> | <div align="right"><small>[[#indice|^top]]</small></div> | ||
==October, 8th== | ==October, 8th== | ||
+ | I76 agar plate showed two/three colonies. It was stored at +4°C; colonies would have been screened the following week. | ||
+ | |||
+ | ---- | ||
+ | |||
+ | Glycerol stock, miniprep and Nanodrop quantification of: | ||
+ | *I79-2: 95,3 ng/ul | ||
+ | |||
+ | This DNA (and that from I55 and I78 too) was sent to BMR Genomics for sequencing. | ||
+ | ---- | ||
+ | <font color='red' size='+2'>We are now moving all our parts to <partinfo>pSB1C3</partinfo> plasmid</font> | ||
+ | |||
<div align="right"><small>[[#indice|^top]]</small></div> | <div align="right"><small>[[#indice|^top]]</small></div> | ||
==October, 9th== | ==October, 9th== | ||
+ | |||
+ | <font color='red' size='+2'>We are now moving all our parts to <partinfo>pSB1C3</partinfo> plasmid</font> | ||
+ | ---- | ||
+ | |||
+ | A new part was cloned with these ones, named I80. It is the basic part to build self-inducible promoters and was obtained with the following ligation: | ||
+ | |||
+ | I80=I3(in <partinfo>pSB1C3</partinfo>) (S-P) + <partinfo>BBa_F2620</partinfo> (X-P) | ||
<div align="right"><small>[[#indice|^top]]</small></div> | <div align="right"><small>[[#indice|^top]]</small></div> | ||
+ | |||
+ | ==October, 10th== | ||
+ | Inoculum into 4 ml LB+Amp of: | ||
+ | *I75-1/2/3 | ||
+ | *I76-1/2 | ||
+ | *I77-1/2/3 | ||
+ | for E-P screening; | ||
+ | *I47 | ||
+ | *I48 | ||
+ | *I49 | ||
+ | for transfer into <partinfo>pSB1C3</partinfo>. | ||
+ | |||
+ | They were let grow at +37°C, 220 rpm. | ||
+ | |||
+ | ---- | ||
+ | Transformation of I80 ligation. It was plated on LB+Cm34 agar plate and let grow ON at +37°C. | ||
+ | |||
+ | ---- | ||
+ | <font color='red' size='+2'>We are now moving all our parts to <partinfo>pSB1C3</partinfo> plasmid</font> | ||
+ | |||
+ | <div align="right"><small>[[#indice|^top]]</small></div> | ||
+ | |||
<!-- table previous next week --> | <!-- table previous next week --> | ||
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<!-- fine table previous next week --> | <!-- fine table previous next week --> | ||
</td> | </td> | ||
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<td width="15%" align="right" valign="top"> | <td width="15%" align="right" valign="top"> |
Latest revision as of 16:38, 23 October 2010
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