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{

ds = '<div id="dairy-text"><h1>Sunday 2013-06-23</h1> Name of participants: Hampus E, Alexander W <h2>Ongoing constructs:</h2> L. reuteri: 4. 100-23-noplasmid L. plantarum: 5. 256-rifR-pAMβ1 E. coli: 23.pCrcSB1C3-Crt-B 24.pSB1C3-Crt-I 25. pSB1C3-CrtY <h2>Todays work</h2> Glycerol stock preparation: Lb4. reuteri 100-23 no plasmid Lb5. plantarum 256 rifR-Pamβ1 23.pCrcSB1C3-Crc-B 24.pSB1C3-Crc-I Restreak: 25. pSB1C3- crtY Plasmidpreparation 23.pCrcSB1C3-Crc-B 24.pSB1C3-Crc-I <h2>Result</h2> O/N: 25.pSB1C3-crtY: One of the overnights did not grow </div>'

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+

else if(id == 'd2013622')

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{

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ds = '<div id="dairy-text"><h1>Saturday 2013-06-22<h1> Name of participants: Nafisa B, Mikael S, Marcus H <h2>Ongoing constructs:</h2> L. reuteri: 1. CF48-pLR581 2. 1063-pLUL631 3. DSM 20016-pVs2 4. 100-23-noplasmid 6. DSM 20016-pLUL63TsA8 7. DSM 20016-pGFP 8. 100-23-pGT232 12. DSM 20016-noplasmid 14. DSM 20016-pLUL631(B?) L. plantarum: 5. 256-rifR-pAMβ1 10. 256-noplasmid 11. 36E-noplasmid E. faecalis: 9. JH2-2 pAMβ1 E. coli: 1. pSB1C3-red 2. pSB3C5-red 6. pSB1K3-red 14. pET13b-zifz:4cl-PBSII:STS 16. pSB1C3-TAL_m 17. pSB1C3-4Cl_m 18. pSB1C3-CHS_m <h2>Todays work</h2> Glycerol stock preparation: 1. pSB1C3-red 2. pSB3C5-red 6. pSB1K3-red Lb6. reuteri DSM 20016-pLUL63TsA8 Lb7. reuteri DSM 20016-pGFP Lb8. reuteri 100-23-pGT232 Lb9. faecalis JH2-2- pAMβ1 Lb10. plantarum 256-noplasmid Lb11. plantarum 36E-noplasmid Lb12. reuteri DSM 20016-noplasmid Lb14. reuteri DSM 20016-pLUL631 (B?) O/N: Lb4. reuteri100-23-noplasmid Lb5. plantarum 256-rifR-pAMβ1 Plasmid preparation: 1. pSB1C3-red 2. pSB3C5-red 6. pSB1K3-red Lb14. DSM 20016-pLUL631 (B?) Lb6. DSM 20016-pLUL63TsA8 Lb7. DSM 20016-pGFP <h2>Results</h2> Plasmid preparation: L. reuteri: Lb14.1 (strain 14, clone 1) DSM 20016-pLUL631 (B?): 10.0 ng/μl Lb14.2 DSM 20016-pLUL631 (B?): 13.6 ng/μl Lb14.3 DSM 20016-pLUL631 (B?): 14.7 ng/μl Lb14.4 DSM 20016-pLUL631 (B?): 28,4 ng/μl Lb6.1 DSM 20016-pLUL63TsA8: 18.7 ng/μl Lb6.2 DSM 20016-pLUL63TsA8: 14.4 ng/μl Lb6.3 DSM 20016-pLUL63TsA8: 12.5 ng/μl Lb6.4 DSM 20016-pLUL63TsA8: 27.7 ng/μl Lb7.2 DSM 20016-pGFP: 29.9 ng/μl Lb7.3 DSM 20016-pGFP: 16.9 ng/μl Lb7.4 DSM 20016-pGFP: 10.9 ng/μl</div>'

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}

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else if(id == 'd2013621')

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{

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ds = '<div id="dairy-text"><h1>Friday 2013-06-21</h1> Name of participants: Stephanie H, Alona N, Anton B, Mikael S, Nafisa B, Anders E, Marcus H, Ken B-A, <h2>Ongoing constructs:</h2> L. reuteri: 1. CF48-pLR581 2. 1063-pLUL631 3. DSM 20016-pVs2 4. 100-23-noplasmid 6. DSM 20016-pLUL63TsA8 7. DSM 20016-pGFP 8. 100-23-pGT232 12. DSM 20016-noplasmid 14. DSM 20016-pLUL631(B?) L. plantarum: 5. 256-rifR-pAMβ1 10. 256-noplasmid 11. 36E-noplasmid E. faecalis: 9. JH2-2 pAMβ1 E. coli: 1. pSB1C3-red 2. pSB3C5-red 6. pSB1K3-red 14. pET13b-zifz:4cl-PBSII:STS 16. pSB1C3-TAL_m 17. pSB1C3-4Cl_m 18. pSB1C3-CHS_m 22. pSB1C3-B0032-BFP <h2>Todays work</h2> Plasmid preparation*: Lb1. reuteri CF48-pLR581 Lb3. reuteri DSM 20016-pVs2 *to get more useable material and to look for different result from clones grown in a lock and a CO2-cupboard. O/N: 1. pSB1C3-red 2. pSB3C5-red 6. pSB1K3-red Lb6. reuteri DSM 20016-pLUL63TsA8 Lb7. reuteri DSM 20016-pGFP Lb14. reuteri DSM 20016-pLUL631(B?) Lb12. reuteri DSM 20016-noplasmid Lb8. reuteri 100-23-pGT232 Lb10. plantarum 256-noplasmid Lb11. plantarum 36E-noplasmid Lb9. faecalis JH2-2 pAMβ1 *- *from the plate without erythromycin. Plasmid preparation: 16. pSB1C3-TAL_m 17. pSB1C3-4Cl_m 18. pSB1C3-CHS_m 22. pSB1C3-B0032-BFP <h2>Results</h2> Previous day: Re-streak: Lb4. reuteri 100-23-noplasmid: No growth. → Grow on non-antibiotic plates Today: Plasmid preparation: Lb1.2 (strain 1, clone 2) reuteri CF48-pLR 581: Non-usable concentration * Lb1.4 reuteri CF48-pLR 581: 161.8 ng/µl * Lb3.8 reuteri DSM 20016 pVS2: 148.5 ng/µl * Lb3.10 reuteri DSM 20016 pVS2: Non-usable concentration * *there is seemingly no correlation between growth in lock vs. CO2-cupboard and plasmid concentration. This seems strange though. Cupboard is not supposed to create an anaerobic environment → do not use cupboard <h2>Other experiments</h2> SET buffer preparation: Lysis buffer preparation: </div>'

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else if(id == 'd201373')

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   {
 	ds = '<div id="dairy-text"><h1>Sunday 2013-06-23</h1><br><b>Name of participants: </b>Hampus E, Alexander W<br><br><h2>Ongoing constructs:</h2><br><b>L. reuteri: </b><br>4. 100-23-noplasmid<br><br><b>L. plantarum:</b><br>5. 256-rifR-pAMβ1<br><br><b>E. coli: </b><br>23.pCrcSB1C3-Crt-B<br>24.pSB1C3-Crt-I<br>25. pSB1C3-CrtY<br><br><h2>Todays work</h2><br><b>Glycerol stock preparation:</b><br>Lb4. reuteri 100-23 no plasmid<br>Lb5. plantarum 256 rifR-Pamβ1<br>23.pCrcSB1C3-Crc-B<br>24.pSB1C3-Crc-I<br><br><b>Restreak:</b><br>25. pSB1C3- crtY<br> <br><b>Plasmidpreparation </b><br>23.pCrcSB1C3-Crc-B<br>24.pSB1C3-Crc-I<br><br><h2>Result</h2><br><b>O/N:</b><br>25.pSB1C3-crtY: One of the overnights did not grow<br></div>'
+ }
+ else if(id == 'd2013622')
+ {
+	ds = '<div id="dairy-text"><h1>Saturday 2013-06-22<h1><br><b>Name of participants: </b>Nafisa B, Mikael S, Marcus H<br><br><h2>Ongoing constructs:</h2><br><b>L. reuteri: </b><br>1. CF48-pLR581<br>2. 1063-pLUL631<br>3. DSM 20016-pVs2<br>4. 100-23-noplasmid<br>6. DSM 20016-pLUL63TsA8<br>7. DSM 20016-pGFP<br>8. 100-23-pGT232<br>12. DSM 20016-noplasmid<br>14. DSM 20016-pLUL631(B?)<br><br><b>L. plantarum:</b><br>5. 256-rifR-pAMβ1<br>10. 256-noplasmid<br>11. 36E-noplasmid<br><br><b>E. faecalis:</b><br>9. JH2-2 pAMβ1<br><br><b>E. coli:</b><br>1. pSB1C3-red<br>2. pSB3C5-red<br>6. pSB1K3-red<br>14. pET13b-zifz:4cl-PBSII:STS<br>16. pSB1C3-TAL_m<br>17. pSB1C3-4Cl_m<br>18. pSB1C3-CHS_m<br><br><h2>Todays work</h2><br><b>Glycerol stock preparation: </b><br>1. pSB1C3-red<br>2. pSB3C5-red<br>6. pSB1K3-red <br>Lb6. reuteri DSM 20016-pLUL63TsA8<br>Lb7. reuteri DSM 20016-pGFP<br>Lb8. reuteri 100-23-pGT232<br>Lb9. faecalis  JH2-2- pAMβ1<br>Lb10. plantarum 256-noplasmid<br>Lb11. plantarum 36E-noplasmid<br>Lb12. reuteri DSM 20016-noplasmid<br>Lb14. reuteri DSM 20016-pLUL631 (B?)<br><br><b>O/N: </b><br>Lb4. reuteri100-23-noplasmid<br>Lb5. plantarum 256-rifR-pAMβ1<br><br><b>Plasmid preparation:</b><br>1. pSB1C3-red<br>2. pSB3C5-red<br>6. pSB1K3-red <br>Lb14. DSM 20016-pLUL631 (B?)<br>Lb6. DSM 20016-pLUL63TsA8<br>Lb7. DSM 20016-pGFP<br><br><h2>Results</h2><br><b>Plasmid preparation:</b><br><b>L. reuteri:</b><br>Lb14.1 (strain 14, clone 1) DSM 20016-pLUL631 (B?): 10.0 ng/μl<br>Lb14.2 DSM 20016-pLUL631 (B?): 13.6 ng/μl<br>Lb14.3 DSM 20016-pLUL631 (B?): 14.7 ng/μl<br>Lb14.4 DSM 20016-pLUL631 (B?): 28,4 ng/μl<br>Lb6.1 DSM 20016-pLUL63TsA8: 18.7 ng/μl<br>Lb6.2 DSM 20016-pLUL63TsA8: 14.4 ng/μl<br>Lb6.3 DSM 20016-pLUL63TsA8: 12.5 ng/μl<br>Lb6.4 DSM 20016-pLUL63TsA8: 27.7 ng/μl<br>Lb7.2 DSM 20016-pGFP: 29.9 ng/μl<br>Lb7.3 DSM 20016-pGFP: 16.9 ng/μl<br>Lb7.4 DSM 20016-pGFP: 10.9 ng/μl</div>'
+ }
+   else if(id == 'd2013621')
+ {
+	ds = '<div id="dairy-text"><h1>Friday 2013-06-21</h1><br><b>Name of participants: </b>Stephanie H, Alona N, Anton B, Mikael S, Nafisa B, Anders E, Marcus H, Ken B-A, <br><br><h2>Ongoing constructs:</h2><br><b>L. reuteri: </b><br>1. CF48-pLR581<br>2. 1063-pLUL631<br>3. DSM 20016-pVs2<br>4. 100-23-noplasmid<br>6. DSM 20016-pLUL63TsA8<br>7. DSM 20016-pGFP<br>8. 100-23-pGT232<br>12. DSM 20016-noplasmid<br>14. DSM 20016-pLUL631(B?)<br><br><b>L. plantarum:</b><br>5. 256-rifR-pAMβ1<br>10. 256-noplasmid<br>11. 36E-noplasmid<br><br><b>E. faecalis:</b><br>9. JH2-2 pAMβ1<br><br><b>E. coli:</b><br>1. pSB1C3-red<br>2. pSB3C5-red<br>6. pSB1K3-red<br>14. pET13b-zifz:4cl-PBSII:STS<br>16. pSB1C3-TAL_m<br>17. pSB1C3-4Cl_m<br>18. pSB1C3-CHS_m<br>22. pSB1C3-B0032-BFP<br><br><h2>Todays work</h2><br><b>Plasmid preparation*: </b><br>Lb1. reuteri CF48-pLR581<br>Lb3. reuteri DSM 20016-pVs2 <br><i>*to get more useable material and to look for different result from clones grown in a lock and a CO2-cupboard.</i><br><br><b>O/N: </b><br>1. pSB1C3-red<br>2. pSB3C5-red<br>6. pSB1K3-red<br>Lb6. reuteri DSM 20016-pLUL63TsA8<br>Lb7. reuteri DSM 20016-pGFP<br>Lb14. reuteri DSM 20016-pLUL631(B?)<br>Lb12. reuteri DSM 20016-noplasmid<br>Lb8. reuteri 100-23-pGT232<br>Lb10. plantarum 256-noplasmid<br>Lb11. plantarum 36E-noplasmid<br>Lb9. faecalis JH2-2 pAMβ1 *-<br><i>*from the plate without erythromycin. </i><br><br><b>Plasmid preparation:</b><br>16. pSB1C3-TAL_m<br>17. pSB1C3-4Cl_m<br>18. pSB1C3-CHS_m<br>22. pSB1C3-B0032-BFP<br><br><h2>Results</h2><br><b>Previous day:</b><br><b>Re-streak: </b><br>Lb4. reuteri 100-23-noplasmid: No growth. → Grow on non-antibiotic plates  <br><br><b>Today:</b><br><b>Plasmid preparation:</b><br>Lb1.2 (strain 1, clone 2) reuteri CF48-pLR 581: Non-usable concentration *<br>Lb1.4 reuteri CF48-pLR 581: 161.8 ng/µl *<br>Lb3.8 reuteri DSM 20016 pVS2: 148.5 ng/µl *<br>Lb3.10 reuteri DSM 20016 pVS2: Non-usable concentration *<br><i>*there is seemingly no correlation between growth in lock vs. CO2-cupboard and plasmid concentration. This seems strange though. Cupboard is not supposed to create an anaerobic environment → do not use cupboard</i><br><br><h2>Other experiments</h2><br><b>SET buffer preparation: </b><br><b>Lysis buffer preparation: </b></div>'
   }
   else if(id == 'd201373')

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