Team:Hong Kong HKUST/notebook/mod2
From 2013.igem.org
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<a href='#' class='head'>Week 3</a> | <a href='#' class='head'>Week 3</a> | ||
- | <div class='content' align="left"> | + | <div class='content' align="left"> |
+ | <p> </p> | ||
+ | <p><strong>August 12 </strong><br /> | ||
+ | Wet lab <br /> | ||
+ | · Miniprep of pCMV+eGFP+ BBa_J176171, followed by digestion check and gel <br /> | ||
+ | · PCR for pCMV cloning from pEGFP-N1 using Vent polymerase, followed by gel check and PCR clean up <br /> | ||
+ | · Digestion check of BBa_J176171+FADR by Xba1, HindIII and Spe1 <br /> | ||
+ | · Ran gel for digestion check <br /> | ||
+ | · pEGFP-N1 digestion for GRP78, extraction pCMV using Ase1 and Xho1, followed by gel check and DNA purification <br /> | ||
+ | · Digestion of BBa_J176171 using single restriction site, Xba1, vector dephosphorylation and ligation with FADR followed by transformation <br /> | ||
+ | · Site direct mutagenesis for BBa_J04450-PSB1C3, followed by gel check before parental digestion with Dpn1 and transformation</p> | ||
+ | <p> </p> | ||
+ | <p><strong>August 13 </strong><br /> | ||
+ | Wet lab <br /> | ||
+ | · Primers phosphorylation for FABP1 Multi-site Mutagenesis using T4 PNK <br /> | ||
+ | · Primers phosphorylation for Site Direct Mutagenesis for BBa_J04450-PSB1C3 using T4 PNK <br /> | ||
+ | · Site Direct Mutagenesis for BBa_J04450-PSB1C3 using phosphorylated primers and non phosphorylated primers <br /> | ||
+ | · Overnight culture for Competent cells <br /> | ||
+ | · pDRIVE_hGRP78 arrival, transformation into <em>E. Coli</em> strain DH10b </p> | ||
+ | <p> </p> | ||
+ | <p><strong>August 14 </strong><br /> | ||
+ | Wet lab <br /> | ||
+ | · Nothing done due the typhoon</p> | ||
+ | <p> </p> | ||
+ | <p><strong>August 15 </strong><br /> | ||
+ | Wet lab <br /> | ||
+ | · pFadBA+pEGFP-N1 ligation, first vector dephosphorylation using Antarctic phosphatase followed by ligation by T4Ligase and transformation into <em>E. Coli</em> SURE strain. <br /> | ||
+ | · pCMV+eGFP+BBa_J176171 digestion check, followed by gel check <br /> | ||
+ | · Repeat GRP78+pEGFP-N1 ligation, followed by transformation into <em>E. Coli</em> DH10b strain. <br /> | ||
+ | · Digestion check for FADR+BBa_J176171 usign Xba1 and HindIII <br /> | ||
+ | · Inoculations of FADR+ BBa_J176171, pCMV+eGFP+ BBa_J176171, pFadBA+pEGFP-N1, pFadBA+eGFP+ BBa_J176171 followed by gel check</p> | ||
+ | <p> </p> | ||
+ | <p><strong>August 16 </strong><br /> | ||
+ | Wet lab <br /> | ||
+ | · Miniprep of FADR+ BBa_J176171, pCMV+eGFP+ BBa_J176171, pFadBA+pEGFP-N1, pFadBA+eGFP+ BBa_J176171 <br /> | ||
+ | · Restriction check for FADR+ BBa_J176171 and pFadBA+pEGFP-N1 followed by gel check <br /> | ||
+ | · Inoculations of FADR+ BBa_J176171, pFadBA+pEGFP-N1, pFadBA+eGFP+ BBa_J176171 <br /> | ||
+ | · DH105alpha <em>E. Coli</em> competent cells preparation</p> | ||
+ | <p> </p> | ||
</div> | </div> | ||
</div> | </div> | ||
<div> | <div> | ||
<a href='#' class='head'>Week 4</a> | <a href='#' class='head'>Week 4</a> | ||
- | <div class='content' align="left"> | + | <div class='content' align="left"> |
+ | <p> </p> | ||
+ | <p><strong>August 19 </strong><br /> | ||
+ | Wet lab <br /> | ||
+ | · Repeat GRP78+pEGFP-N1 ligation, followed by transformation into <em>E. Coli</em> DH10b strain. <br /> | ||
+ | · Miniprep of FADR+ BBa_J176171, pFadBA+pEGFP-N1, pFadBA+eGFP+ BBa_J176171 <br /> | ||
+ | · Restriction check for pFadBA+pEGFP-N1 followed by gel check <br /> | ||
+ | · Restriction check for FADR+ BBa_J176171 and pFadBA+pEGFP-N1 followed by gel check <br /> | ||
+ | · Streak colony with the right FADR+BBa_J176171 construct <br /> | ||
+ | · DH5alpha <em>E. Coli </em>competent cells preparation <br /> | ||
+ | · <br /> | ||
+ | </p> | ||
+ | <p><strong>August 20</strong><br /> | ||
+ | Wet lab <br /> | ||
+ | · Digestion check pFadBA+pEGFP-N1 with Pst1, Xba1. Followed by gel check <br /> | ||
+ | · Digestion check for damaged plates of GRP78+pEGFP-N1 using Xba1 <br /> | ||
+ | · Digestion check of pFadBA+eGFP+ BBa_J176171 using Age1HF, HindIII and Xba1 <br /> | ||
+ | · Site Direct Mutagenesis for illegal restriction sites for FABP1 <br /> | ||
+ | · Inoculate GRP78+pEGFP-N1, pCMV+eGFP+BBa_J176171 <br /> | ||
+ | · DH10b <em>E. Coli</em> competent cells preparation</p> | ||
+ | <p> </p> | ||
+ | <p><strong>August 21 </strong><br /> | ||
+ | Wet lab <br /> | ||
+ | · Miniprep GRP78+pEGFP-N1, followed by digestion check and gel check using Spe1 <br /> | ||
+ | · Miniprep pCMV+eGFP+BBa_J176171 followed by digestion check using Nde1 and Age1HF <br /> | ||
+ | · Digestion check of pFadBA+eGFP+BBa_J176171 using Nde1 , FADR+ BBa_J176171 using Age1 <br /> | ||
+ | · Site direct Mutagenesis for FABP1+eGFP+BBa_J176171 <br /> | ||
+ | · PCR for GRP78 promoter cloning from pDRIVE_hGRP78, followed by gel check PCR clean up, digestion using Ase1 and Xho1 and DNA purification</p> | ||
+ | <p> </p> | ||
+ | <p><strong>August 22 </strong><br /> | ||
+ | Wet lab <br /> | ||
+ | · DH10b <em>E. Coli</em> competent cells preparation <br /> | ||
+ | · Site direct Mutagenesis for FABP1+eGFP+BBa_J176171 with phosphorylated primers, followed by gel check before Dpn1 parental string digestion <br /> | ||
+ | · Ligation of GRP78 and pEGFP-N1, first vector dephophorylation and ligation with T4Ligase. Transformed into <em>E. Coli</em> DH10b strain <br /> | ||
+ | · Transformation of pBlueScript KS (+) in to SURE <em>E. Coli</em> <br /> | ||
+ | Dry lab <br /> | ||
+ | · Discuss about FABP1 construct vanishing under PCR conditions</p> | ||
+ | <p> </p> | ||
+ | <div> </div> | ||
+ | <p> </p> | ||
</div> | </div> | ||
</div> | </div> | ||
+ | <div> | ||
+ | <a href='#' class='head'>Week 5</a> | ||
+ | <div class='content' align="left"> | ||
+ | <p> </p> | ||
+ | <p><strong>August 26 </strong><br /> | ||
+ | Wet lab <br /> | ||
+ | · FABP1 assessment under PCR conditions <br /> | ||
+ | · BBa_J176171+eGFP assessment under PCR conditions <br /> | ||
+ | · BBa_J176171bassessment under PCR conditions <br /> | ||
+ | · Temperature gradient for FABP1+BBa_J176171+eGFP construct <br /> | ||
+ | · Inoculate pBlueScript KS (+)</p> | ||
+ | <p> </p> | ||
+ | <p><strong>August 27 </strong><br /> | ||
+ | Wet lab <br /> | ||
+ | · DH10b <em>E. Coli</em> competent cells preparation</p> | ||
+ | <p> </p> | ||
+ | <p><strong>August 28 </strong><br /> | ||
+ | Wet lab <br /> | ||
+ | · BBa_J176171bassessment under PCR conditions <br /> | ||
+ | · Temperature gradient for FABP1+BBa_J176171+eGFP construct <br /> | ||
+ | · PCR for FABP1 promoter cloning from gDNA <br /> | ||
+ | · GRP78 ligation to dephosphorylated pEGFP-N1, ligation done using T4 Ligase, transformed into <em>E.Coli</em> DH10b <br /> | ||
+ | · Miniprep pBlueScript KS (+) <br /> | ||
+ | · Digest pBlueScript KS (+) with Xba1 and BamH1HF <br /> | ||
+ | · Restreak BBa_J176171 and inoculate it</p> | ||
+ | <p> </p> | ||
+ | <p><strong>August 29 </strong><br /> | ||
+ | Wet lab <br /> | ||
+ | · Miniprep estreaked BBa_J176171 <br /> | ||
+ | · GRP78 ligation to dephosphorylated pEGFP-N1, ligation done using T4 Ligase, transformed into <em>E.Coli</em> DH10b <br /> | ||
+ | · Ligation of FABP1 in to pBlueScript KS (+) using T4 Ligase followed by transformation into DH10b <em>E. Coli</em> <br /> | ||
+ | · Transformation of BBa_J176171 into SURE <em>E. Coli</em></p> | ||
+ | <p> </p> | ||
+ | <p><strong>August 30 </strong><br /> | ||
+ | Wet lab <br /> | ||
+ | · Inoculate GRP78+pEGFP-N1 <br /> | ||
+ | · Inoculate FABP1+pBlueScript KS (+) <br /> | ||
+ | · Inoculate BBa_J176171 <br /> | ||
+ | · PCR conditions check for BBa_J176171 looking for heat degradation</p> | ||
+ | <p> </p> | ||
+ | <p><strong>August 31 </strong><br /> | ||
+ | Wet lab <br /> | ||
+ | · Miniprep of FABP1+pBlueScript KS (+), BBa_J176171 <br /> | ||
+ | · PCR conditions check for BBa_J176171 looking for heat degradation</p> | ||
+ | </div> | ||
+ | </div> | ||
+ | |||
</div><div id="satu" align="center"> <h1>September 2013</h1> | </div><div id="satu" align="center"> <h1>September 2013</h1> | ||
Revision as of 15:28, 19 September 2013
![](https://static.igem.org/mediawiki/igem.org/c/c7/BANNER1_%281%29.png)
June 2013
June 24
Wet lab
· Inoculation of pBlueScript KS(+) for training
· Autoclave basic materials
· Preparing LB
· LB-Ampicillin plates poured Dry lab
Protocols review
June 25
Wet lab
· Plasmid extraction of pBlueScript KS(+)
· LB-Chloramphenicol plates poured
Dry lab
· Primers design for FABP1, PPARa, GRP78
· Informal meeting
June 26
Wet lab
· Extraction of gDNA from HepG2 Cells for FABP1 and PPARa
· Transformation of pEGFP-N1 and BBa_K817002 (pFadBA)
June 27
Wet lab
· Inoculation of pEGFP-N1 and BBa_K817002 (pFadBA) for plasmid extraction
June 28
Wet lab
· Extraction of pEGFP-N1 and BBa_K817002 (pFadBA) plasmids by miniprep
· Restriction of pEGFP-N1 Restriction digestion by Ase1 and bamH1 for PPARa; Ase1 and Xho1 for GRP78, Xba1 and BamH1 for FABP1, Pst1 and Not1; followed by gel check, extraction and purification
· Restriction of c(pFadBA) by EcoR1 and Pst1
· Ran 0.8% gel for pEGFP-N1 and 2% gel for BBa_K817002 (pFadBA)
June 30
Dry lab
Experiment planning and protocols revision for next week work
July 2013
July 2
Wet lab
· Digestion of pEGFP-N1 by Ase1 and bamH1 for PPARa; , Xba1 and BamH1 for FABP1
· LB-Chloramphenicol plates (the previous ones were found contaminated)
· Inoculation of pEGFP-N1 for plasmid extraction
· Transformation of pFadBA due chloramphenicol plates contamination
July 3
· Extraction of pEGFP-N1 plasmids by miniprep
· PCR for PPARa promoter amplification
· Digestion of pEGFP-N1 by Ase1 and bamH1 for PPARa; , Xba1 and BamH1 for FABP1
July 4
Wet lab
· Inoculation of BBa_K817002 pFadBA
· PCR for PPARa and FABP1 promoter cloning from gDNA
· Ran gel for digestion of pEGFP-N1 by Ase1 and bamH1 for PPARa; Xba1 and BamH1 for FABP1; Ase1 and Xhol1 for GRP78
July 5
Wet lab
· Extraction of BBa_K817002 (pFadBA)
· Inoculation of pEGFP-N1
· PCR for PPARa and FABP1 promoter cloning from gDNA
· Gel check, 0.8% gel for previously gDNA extraction
· Ran gel for PCR check of PPARa and FABP1
· Poured new LB-Kanamycin plates
· Transformation of BBa_J176171
Dry lab
· Discussion about re-design constructions, possible change for BBa_J176171 as mammalian expression vector
· Primer redesign for PPARa and FABP1
July 8
Wet lab
· gDNA extraction from HepG2 cells
· Restriction of BBa_K817002 pFAdBA
· Gel check for gDNA extraction
· Inoculation of BBa_J176171, BBa_K817002 (pFadBA), pEGFP-N1 for plasmid extraction
· New primers for PPARa and FABP1 arrival
· Ran gel for BBa_K817002 pFadBA restriction check, gel extraction and purification
July 9
Wet lab
· Extraction of BBa_J176171, BBa_K817002 pFadBA and pEGFP-N1 by miniprep
· Restriction of pEGFP-N1 Restriction digestion by Ase1 and bamH1 for PPARa; Ase1 and Xho1 for GRP78, Xba1 and BamH1 for FABP1, Pst1 and Not1; followed by gel check, extraction and purification
· Restriction of BBa_J176171 for pFadBA Ase1 and BamH1; FABP1 by Xba1 and Not1
· Ran gel for pEGFP-N1 and BBa_J176171 restriction products
· PCR PPARa and FABP1 promoters cloning from gDNA
· BBa_J52034 (FADR) transformation
July 10
Wet lab
· Ran gel for PCR check of PPARa and FAPB1
· PCR for FABP1, PCR replication
· BBa_J176171 vector dephosphorylation by antartic phosphatase
· Ligation of BBa_K817002 and pFadBA and BBa_J176171
· BBa_J52034 (FADR) inoculation
· Digestion for BBa_K817002 pFadBA extraction
Gel check for BBa_K817002 pFadBA extraction
July 11
Wet lab
· Gel purification for BBa_K817002 pFadBA extraction
· Gel check for FABP1 PCR product
· PCR clean-up
· BBa_J52034 (FADR) miniprep
· BBa_J52034 restriction by Pst1 HF and Not1 HF
· PCR for PPARa
Dry lab
Re-design constructions, now using BBa_J176171 as mammalian expression vector for all related constructions
July 12
Wet lab
· Digestion of FABP1 PCR product
· Ran gel for PCR check of PPARa
· Digest pEGFP-n1 for BBa_J52034 FADR
· Ran gel for pEGFP-n1 for BBa_J52034 FADR followed by gel purification
· BBa_J176171 vector dephosphorylation by Antarctic phosphatase for FABP1 and FADR
Dry Lab
Primers design for pCMV cloning for FADR expression
July 15
Wet lab
· Ligation of FABP1 eGFP and BBa_J176171, using 3 pieces ligation
· Transformation of FABP1 eGFP and BBa_J176171 ligation
· FABP1+eGFP +BBa_J176171 ligation restriction check
July 16
Wet Lab
· Miniprep for full construct of FABP1 and pEGFP-N1
· FADR and pEGFP-N1 Backbone parts ligation
· Plasmids extraction for pCMV cloning for FADR
· BBa_K817002 pFadBA promoter extraction by EcoR1 and Pst1 HF
· BBa_J52034 restriction by EcoR1 and Pst1 HF
· Inoculations for full construct of FABP1 and pEGFP-N1
· Streak colonies containing the right construct for FABP1
July 17
Wet lab
· Plasmid extraction for FABP1+eGFP+BBa_J176171 by miniprep
· Repeat FadR and pFadBA constructs
· Digest pEGFP-n1 and BBa-J176171 for FADR
· Digestion for BBa_K817002 (pFadBA) extraction
· Gel check and gel extraction for BBa_J176171 for FADR and BBa_K817002 (pFadBA)
July 18
Wet lab
· Gel purification for all digested products
· FABP1 digestion check for whole construct prior transfection
· pFadBA vector de phosphorylation and ligation with eGFP and BBa_J176171
· Transformation of pFadBA+eGFP+BBa_J176171
July 19
Wet lab
· FABP1 preparation for transfection
· Ligation of pFadBA and BBa_J176171 followed by transformation
· PCR for PPARa cloning
Dry lab
· Design for characterization of the transfected cells with FABP1 construct
· Review for Multiple Sites Mutagenesis
· Ordered primers for pCMV cloning from pEGFP-N1
July 22
Wet lab
· FABP1 given for characterization and transfection
· Further colony screening for FABP1 construct, inoculations
· Inoculation of pFadBA and BBa_J176171
· Ran gel for PPARa PCR products
July 23
Wet lab
· Primers arrival for pCMV cloning
· PCR for pCMV cloning
· Digestion and gel for construction check for FABP1
· pFadBA gel extraction and purification, followed by vector dephosphorylation BBa_J176171 and ligation, then transformation
· Digestion of pEGFP-N1 for FADR, followed by gel check and extraction
July 24
Wet lab
· DNA purification from gel extraction for digested pEGFP-N1
· Multiple sites mutagenesis for illegal restriction sites for FABP1
· Ran gel for pCMV cloning from pEGFP-N1
· PCR clean up for pCMV cloning from pEGFP-N1
· PCR for PPARa with new primers using Taq polymerase
· Transformation of mutagenesis products
· Inoculation of pFadBA ligation colonies
July 25
Wet lab
· Ran gel check PPARa PCR cloning with new primers using Taq polymerase
· Minprep of pFadBA+eGFP+BBa_J176171 ligation colonies, followed by digestion check
July 26
Wet lab
· Multiple sites mutagenesis for illegal restriction sites for FABP1
· Ran gel before parental string digestion of mutagenesis products
· Digestion of pEGFP-N1 by Apa1 and Xba1 followed by gel check
· Plasmids preparation according to transfection requirements, construct and controls
July 30
Wet lab
· PPARa PCR cloning with new primers using Vent polymerase
· Restriction check for pEGFP-N1, using EcoR1, Xba1, Spe1 and Pst1
· BBa_J176171 vector de phosphorylation, followed by ligation with eGFP using T4 Ligase, then transformation into E. Coli strain DH10b
· PCR for PPARa with new primers using Vent polymerase
Dry lab
· Discussion and re assessment of constructs related to pEGFP-N1
July 31
· Ran gel check for PPARa PCR cloning with new primers using Vent polymerase
· PCR for pCMV cloning from pEGFP-N1, followed by gel check and PCR clean up
· PCR for PPARa with reference primers using Vent polymerase
· Ran gel check for PPARa PCR cloning with reference primers using Vent polymerase
August 2013
August 2
Wet lab
· Restriction check for EGFP+ BBa_J176171 using EcoR1 and Pst1HF
· Consensus Kozak sequence extraction from BBa_J176171 by EcoR1 and Xba1, followed by gel check and DNA purification
· PCR for PPARa, using temperature gradient and every available set of primers designed, using Vent polymerase
· Genomic DNA extraction from HepG2 cells, Phenol/Chloroform protocol
August 5
Wet lab
· Gel Check for PPARa PCR promoter cloning, using temperature gradient and every available set of primers designed.
· Digestion of BBa_J176171 using single restriction site, Xba1, vector dephosphorylation and ligation with FADR followed by transformation
· Ligation check of pFadBA+BBa_J176171+eGFP using Age1
· PCR for PPARa, using temperature gradient and every available set of primers designed, using Taq polymerase
· gDNA Gel check
Dry lab
· Primers design for BBa_J04450-PSB1C3 Xba1 restriction site removal by site direct mutagenesis
August 6
Wet lab
· Ran gel for PCR for PPARa, using temperature gradient and every available set of primers designed, using Taq polymerase
· Inoculation of FADR+BBa_J176171
August 7
Wet lab
· Digestion check of BBa_J176171+eGFP by Not1 and Pst1
· Digestion check of BBa_J176171+FADR by Xba1 and HindIII
· Ran gel for digestion check
· Inoculation of FADR+BBa_J176171, colony screening
August 8
Wet lab
· Miniprep for FADR+BBa_J176171, colony screening
· Digestion check of BBa_J176171+FADR by Xba1 and HindIII
· Ran gel for digestion check
· Inoculation of FADR+BBa_J176171, colony screening
· pCMV from cloned from pEGFP-N1adding restriction sites for ligation with eGFP and BBa_J176171, followed by transformation
August 9
Wet lab
· Primers arrival for BBa_J04450-PSB1C3 for site direct mutagenesis
· Digestion check of BBa_J176171+FADR Xba1 and HindIII, Xba1 and Spe1
· Ran gel for digestion check
· Site direct Mutagenesis for BBa_J04450-PSB1C3 removing Xba1 restriction site, followed by gel check before parental string digestion and transformation
· Inoculation of pCMV from cloned from pEGFP-N1adding restriction sites for ligation with eGFP and BBa_J176171
August 12
Wet lab
· Miniprep of pCMV+eGFP+ BBa_J176171, followed by digestion check and gel
· PCR for pCMV cloning from pEGFP-N1 using Vent polymerase, followed by gel check and PCR clean up
· Digestion check of BBa_J176171+FADR by Xba1, HindIII and Spe1
· Ran gel for digestion check
· pEGFP-N1 digestion for GRP78, extraction pCMV using Ase1 and Xho1, followed by gel check and DNA purification
· Digestion of BBa_J176171 using single restriction site, Xba1, vector dephosphorylation and ligation with FADR followed by transformation
· Site direct mutagenesis for BBa_J04450-PSB1C3, followed by gel check before parental digestion with Dpn1 and transformation
August 13
Wet lab
· Primers phosphorylation for FABP1 Multi-site Mutagenesis using T4 PNK
· Primers phosphorylation for Site Direct Mutagenesis for BBa_J04450-PSB1C3 using T4 PNK
· Site Direct Mutagenesis for BBa_J04450-PSB1C3 using phosphorylated primers and non phosphorylated primers
· Overnight culture for Competent cells
· pDRIVE_hGRP78 arrival, transformation into E. Coli strain DH10b
August 14
Wet lab
· Nothing done due the typhoon
August 15
Wet lab
· pFadBA+pEGFP-N1 ligation, first vector dephosphorylation using Antarctic phosphatase followed by ligation by T4Ligase and transformation into E. Coli SURE strain.
· pCMV+eGFP+BBa_J176171 digestion check, followed by gel check
· Repeat GRP78+pEGFP-N1 ligation, followed by transformation into E. Coli DH10b strain.
· Digestion check for FADR+BBa_J176171 usign Xba1 and HindIII
· Inoculations of FADR+ BBa_J176171, pCMV+eGFP+ BBa_J176171, pFadBA+pEGFP-N1, pFadBA+eGFP+ BBa_J176171 followed by gel check
August 16
Wet lab
· Miniprep of FADR+ BBa_J176171, pCMV+eGFP+ BBa_J176171, pFadBA+pEGFP-N1, pFadBA+eGFP+ BBa_J176171
· Restriction check for FADR+ BBa_J176171 and pFadBA+pEGFP-N1 followed by gel check
· Inoculations of FADR+ BBa_J176171, pFadBA+pEGFP-N1, pFadBA+eGFP+ BBa_J176171
· DH105alpha E. Coli competent cells preparation
August 19
Wet lab
· Repeat GRP78+pEGFP-N1 ligation, followed by transformation into E. Coli DH10b strain.
· Miniprep of FADR+ BBa_J176171, pFadBA+pEGFP-N1, pFadBA+eGFP+ BBa_J176171
· Restriction check for pFadBA+pEGFP-N1 followed by gel check
· Restriction check for FADR+ BBa_J176171 and pFadBA+pEGFP-N1 followed by gel check
· Streak colony with the right FADR+BBa_J176171 construct
· DH5alpha E. Coli competent cells preparation
·
August 20
Wet lab
· Digestion check pFadBA+pEGFP-N1 with Pst1, Xba1. Followed by gel check
· Digestion check for damaged plates of GRP78+pEGFP-N1 using Xba1
· Digestion check of pFadBA+eGFP+ BBa_J176171 using Age1HF, HindIII and Xba1
· Site Direct Mutagenesis for illegal restriction sites for FABP1
· Inoculate GRP78+pEGFP-N1, pCMV+eGFP+BBa_J176171
· DH10b E. Coli competent cells preparation
August 21
Wet lab
· Miniprep GRP78+pEGFP-N1, followed by digestion check and gel check using Spe1
· Miniprep pCMV+eGFP+BBa_J176171 followed by digestion check using Nde1 and Age1HF
· Digestion check of pFadBA+eGFP+BBa_J176171 using Nde1 , FADR+ BBa_J176171 using Age1
· Site direct Mutagenesis for FABP1+eGFP+BBa_J176171
· PCR for GRP78 promoter cloning from pDRIVE_hGRP78, followed by gel check PCR clean up, digestion using Ase1 and Xho1 and DNA purification
August 22
Wet lab
· DH10b E. Coli competent cells preparation
· Site direct Mutagenesis for FABP1+eGFP+BBa_J176171 with phosphorylated primers, followed by gel check before Dpn1 parental string digestion
· Ligation of GRP78 and pEGFP-N1, first vector dephophorylation and ligation with T4Ligase. Transformed into E. Coli DH10b strain
· Transformation of pBlueScript KS (+) in to SURE E. Coli
Dry lab
· Discuss about FABP1 construct vanishing under PCR conditions
August 26
Wet lab
· FABP1 assessment under PCR conditions
· BBa_J176171+eGFP assessment under PCR conditions
· BBa_J176171bassessment under PCR conditions
· Temperature gradient for FABP1+BBa_J176171+eGFP construct
· Inoculate pBlueScript KS (+)
August 27
Wet lab
· DH10b E. Coli competent cells preparation
August 28
Wet lab
· BBa_J176171bassessment under PCR conditions
· Temperature gradient for FABP1+BBa_J176171+eGFP construct
· PCR for FABP1 promoter cloning from gDNA
· GRP78 ligation to dephosphorylated pEGFP-N1, ligation done using T4 Ligase, transformed into E.Coli DH10b
· Miniprep pBlueScript KS (+)
· Digest pBlueScript KS (+) with Xba1 and BamH1HF
· Restreak BBa_J176171 and inoculate it
August 29
Wet lab
· Miniprep estreaked BBa_J176171
· GRP78 ligation to dephosphorylated pEGFP-N1, ligation done using T4 Ligase, transformed into E.Coli DH10b
· Ligation of FABP1 in to pBlueScript KS (+) using T4 Ligase followed by transformation into DH10b E. Coli
· Transformation of BBa_J176171 into SURE E. Coli
August 30
Wet lab
· Inoculate GRP78+pEGFP-N1
· Inoculate FABP1+pBlueScript KS (+)
· Inoculate BBa_J176171
· PCR conditions check for BBa_J176171 looking for heat degradation
August 31
Wet lab
· Miniprep of FABP1+pBlueScript KS (+), BBa_J176171
· PCR conditions check for BBa_J176171 looking for heat degradation