Glasgow/Wetlab/Week7

From 2007.igem.org

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| pCR4 ||XylR & Pr || [https://2007.igem.org/Glasgow/Wetlab/Orders Pr_Prefix_1] & [https://2007.igem.org/Glasgow/Wetlab/Orders XylR_Suffix_1]
| pCR4 ||XylR & Pr || [https://2007.igem.org/Glasgow/Wetlab/Orders Pr_Prefix_1] & [https://2007.igem.org/Glasgow/Wetlab/Orders XylR_Suffix_1]
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Overnight cultures were seeded from colonies that gave successful PCR results in order to miniprep the plasmids tomorrow.
Overnight cultures were seeded from colonies that gave successful PCR results in order to miniprep the plasmids tomorrow.
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| pSB1AC3 (3/20G) || DntR || [https://2007.igem.org/Glasgow/Wetlab/Orders DntR_Prefix_1] & [https://2007.igem.org/Glasgow/Wetlab/Orders DntR_Suffix_2]
| pSB1AC3 (3/20G) || DntR || [https://2007.igem.org/Glasgow/Wetlab/Orders DntR_Prefix_1] & [https://2007.igem.org/Glasgow/Wetlab/Orders DntR_Suffix_2]
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Overnight cultures were seeded from colonies that gave successful PCR results in order to miniprep the plasmids tomorrow.
Overnight cultures were seeded from colonies that gave successful PCR results in order to miniprep the plasmids tomorrow.
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[[User:Mojs|Maia]] took the following BioBricks from the kit plates and transformed into ''E. coli'' TOP10 cells:
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[[User:Mojs|Maia]] took the following BioBricks from the kit plates and transformed (see [[Glasgow/Wetlab/Protocols#Protocol 2: Transforming BioBricks|Protocol 2]]) into ''E. coli'' TOP10 cells:
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|[http://partsregistry.org/Part:BBa_E0432 Bba_E0432] || EYFP + RBS + terminator + LVA tag || ''E. coli''  TOP10 || pSB1A2 || 4/11C
|[http://partsregistry.org/Part:BBa_E0432 Bba_E0432] || EYFP + RBS + terminator + LVA tag || ''E. coli''  TOP10 || pSB1A2 || 4/11C
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=== Tuesday 14th August 2007 ===
=== Tuesday 14th August 2007 ===

Revision as of 20:16, 15 August 2007

Back To Main Page | Back To Wetlab Log


Contents

Week 7

Monday 13th August 2007

  1. Lynsey did colony PCR (see Protocol 9) on the following E. coli TOP10 transformants to check that their plasmids carry our expected inserts:

    Plasmid Expected Insert Primers
    pCR4 Pu Pu_Prefix_After & Pu_Suffix_After
    pCR4 Pu Pu_Prefix_Emma & Pu_Suffix_Emma
    pCR4 Pr Pr_Prefix_1 & Pr_Suffix_1
    pCR4 XylR XylR_Prefix_1 & XylR_Suffix_1
    pCR4 XylR & Pr Pr_Prefix_1 & XylR_Suffix_1


    Overnight cultures were seeded from colonies that gave successful PCR results in order to miniprep the plasmids tomorrow.

  2. Maija did colony PCR (see Protocol 9) on the following E. coli DB3.1 transformants to check that their plasmids carry our expected inserts:

    Plasmid Expected Insert Primers
    pSB3K5 (4/6B) (*m*) B1 17 (*m*)_for_1 & BBs_Methyl_2
    pSB1AC3 (3/20G) (*m*) B1 17 (*m*)_for_1 & BBs_Methyl_2
    pSB3K5 (4/6B) (*m*) C5 24 (*m*)_for_1 & (*m*)_rev_1
    pSB1AC3 (3/20G) (*m*) (*m*)_for_1 & (*m*)_rev_1
    pSB3K5 (4/6B) DntR DntR_Prefix_1 & DntR_Suffix_2
    pSB1AC3 (3/20G) DntR DntR_Prefix_1 & DntR_Suffix_2


    Overnight cultures were seeded from colonies that gave successful PCR results in order to miniprep the plasmids tomorrow.

  3. Maia took the following BioBricks from the kit plates and transformed (see Protocol 2) into E. coli TOP10 cells:

    BioBrick Part Function Chassis Plasmid Kit Plate Location (Plate/Well)
    Bba_B0014 Double terminator E. coli TOP10 pSB1AK3 1/1G
    Bba_B0015 Double terminator E. coli TOP10 pSB1AK3 1/1I
    " " " " 3/3O
    Bba_J61100 RBS E. coli TOP10 pSB1A2 4/12N
    Bba_J61101 RBS E. coli TOP10 pSB1A2 4/12J
    Bba_J61102 RBS E. coli TOP10 pSB1A2 4/12L
    Bba_J61103 RBS E. coli TOP10 pSB1A2 4/12P
    Bba_E0430 EYFP + RBS + terminator E. coli TOP10 pSB1A2 1/11A
    Bba_E0422 ECFP + RBS + terminator + LVA tag E. coli TOP10 pSB1AK3 1/11G
    Bba_E0432 EYFP + RBS + terminator + LVA tag E. coli TOP10 pSB1A2 4/11C


    Tuesday 14th August 2007

    Wednesday 15th August 2007

    Thursday 16th August 2007

    === Friday 17th August 2007 ===