Team:Nevada/Notebook
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- | { | + | {{Nevada_css}} |
- | + | [[Image:UNR Notebook.png|border|left|950px]] | |
- | + | ||
- | + | ||
- | + | {{Nevada_topbar}} | |
+ | <div style="padding: 10px 10px 30px 10px;"> | ||
- | + | <p> </p> | |
- | + | <p> </p> | |
+ | <p style="text-align:left;"><span style="font-family:Arial;font-size:16pt;font-style:italic;font-weight:none;text-decoration:italic;color:#15317E;background-color:ffffff;">Team Nevada Notebook</span> | ||
+ | </p> | ||
+ | ---- | ||
+ | ==APRIL== | ||
+ | '''Week of April 11-17:''' | ||
- | + | * ''Christian'' | |
- | + | **Transformed pBIB into Top 10 Cells | |
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* ''Bryson, Michael, Senny, Tyler'' | * ''Bryson, Michael, Senny, Tyler'' | ||
Line 31: | Line 21: | ||
'''Week of April 18-24:''' | '''Week of April 18-24:''' | ||
- | * ''Bryson'' | + | * ''Bryson, Christian'' |
** EcoRI digest of pBIB | ** EcoRI digest of pBIB | ||
** Made Na acetate buffer | ** Made Na acetate buffer | ||
- | + | * ''Christian'' | |
+ | ** Ran gel of EcoR1 Digested pBIB | ||
+ | ==MAY== | ||
'''Week of April 25-May 1:''' | '''Week of April 25-May 1:''' | ||
* ''Bryson'' | * ''Bryson'' | ||
** Ran agarose gel of EcoRI digest | ** Ran agarose gel of EcoRI digest | ||
+ | |||
+ | * ''Matthew'' | ||
+ | ** Team collaborated on pBIB assignment. Too many chefs in the kitchen. | ||
+ | ** We decide to each tackle the pBIB problem in parallel | ||
'''Week of May 2-8:''' | '''Week of May 2-8:''' | ||
Line 47: | Line 43: | ||
** Spread for colonies | ** Spread for colonies | ||
** Did miniprep for pBIB liquid cultures | ** Did miniprep for pBIB liquid cultures | ||
+ | |||
+ | * ''Matthew'' | ||
+ | ** Miniprepped pBIB | ||
+ | ** Ran EcoRI digest and Klenow | ||
+ | ** Ethanol precipitated and ligated | ||
'''Week of May 9-15:''' | '''Week of May 9-15:''' | ||
+ | |||
+ | * ''Christian'' | ||
+ | ** EcoR1/Xba1 Digest of pBIB | ||
+ | ** Did Mini prep on 4 cultures | ||
* ''Bryson'' | * ''Bryson'' | ||
Line 59: | Line 64: | ||
** Did a miniprep and a Phenol:chloroform clean-up | ** Did a miniprep and a Phenol:chloroform clean-up | ||
** Ran 0.8% gel of the XbaI and EcoRI digest with the uncut pBIB | ** Ran 0.8% gel of the XbaI and EcoRI digest with the uncut pBIB | ||
+ | |||
+ | * ''Matthew'' | ||
+ | ** Ligated and transformed | ||
+ | ** Screened colonies, miniprepped, and digested, ran on gel | ||
+ | ** No candidates had EcoRI eliminated | ||
'''Week of May 16-22:''' | '''Week of May 16-22:''' | ||
+ | |||
+ | * ''Christian'' | ||
+ | ** Generated glycerol stock of pBIB transformed Top 10 cells | ||
+ | ** Inoculated 5 cultures of pBIB transformed Top 10 cells grown on Kan resistant plates | ||
+ | ** Ran samples on gel after digest with EcoR1 | ||
* ''Bryson'' | * ''Bryson'' | ||
Line 74: | Line 89: | ||
** Made 50mg/ml stock of KAN | ** Made 50mg/ml stock of KAN | ||
** Made 1X TAE buffer | ** Made 1X TAE buffer | ||
+ | |||
+ | * ''Matthew'' | ||
+ | ** Digested and tested more colonies, none worked | ||
+ | ** Started over with pBIB and Klenow | ||
+ | ** Ethanol precipitated and ligated | ||
+ | ** Transformed | ||
+ | ** Screened colonies, miniprepped, and digested, ran on gel | ||
+ | ** No candidates had EcoRI eliminated | ||
'''Week of May 23-29:''' | '''Week of May 23-29:''' | ||
+ | |||
+ | * ''Christian'' | ||
+ | ** Miniprep on pBIB transformed Top 10 cells using "low copy #" modification | ||
+ | ** Digested with EcoR1 and HindIII | ||
* ''Bryson'' | * ''Bryson'' | ||
Line 93: | Line 120: | ||
** Maxiprepped pBIB vector using QIAGEN QIAfilter Plasmid Maxi Kit | ** Maxiprepped pBIB vector using QIAGEN QIAfilter Plasmid Maxi Kit | ||
+ | * ''Matthew'' | ||
+ | ** Investigated alternative ways of eliminating EcoRI site. | ||
+ | ** Want to try hexameric linkers | ||
+ | |||
+ | ==JUNE== | ||
'''Week of May 30-June 5:''' | '''Week of May 30-June 5:''' | ||
+ | |||
+ | * ''Christian'' | ||
+ | ** Miniprep Top 10 Cells transformed with pBIB | ||
* ''Bryson'' | * ''Bryson'' | ||
Line 122: | Line 157: | ||
** Gel analyzed resultant ccdB PCR reaction with 1.2% agarose gel | ** Gel analyzed resultant ccdB PCR reaction with 1.2% agarose gel | ||
*** Reaction was unsuccessful | *** Reaction was unsuccessful | ||
+ | |||
+ | * ''Matthew'' | ||
+ | ** Miniprepped pBIB | ||
+ | ** Ran EcoRI digests | ||
+ | ** Ran ethanol precipitation | ||
+ | ** Ligated with several concentrations of hexameric linkers designed to destroy site | ||
+ | ** Ran transformation, no colonies | ||
+ | *** Believed procedures/conditions ran on ligation and transformation not ideal | ||
'''Week of June 6-12:''' | '''Week of June 6-12:''' | ||
+ | |||
+ | * ''Christian'' | ||
+ | ** Klenow reaction on EcoR1 digested pBIB | ||
+ | ** T4 ligation on Klenow products | ||
* ''Bryson'' | * ''Bryson'' | ||
Line 138: | Line 185: | ||
** Ran PCR for ccdB using HiFi DNA polymerase (Invitrogen) | ** Ran PCR for ccdB using HiFi DNA polymerase (Invitrogen) | ||
** Gel analyzed resultant ccdB PCR reaction with 1.2% agarose gel and successfully amplified ccdB gene | ** Gel analyzed resultant ccdB PCR reaction with 1.2% agarose gel and successfully amplified ccdB gene | ||
+ | |||
+ | https://static.igem.org/mediawiki/2010/7/76/PCR_ccdB_confirmation.png | ||
+ | |||
** Maxiprepped pBIB vector using QIAGEN QIAfilter Plasmid Maxi Kit | ** Maxiprepped pBIB vector using QIAGEN QIAfilter Plasmid Maxi Kit | ||
+ | |||
+ | * ''Matthew'' | ||
+ | ** Miniprepped pBIB | ||
+ | ** Ran Digestions and ethanol precipitation | ||
+ | ** Ligated with hexameric linkers | ||
+ | ** Transformed, had some colonies | ||
'''Week of June 13-19:''' | '''Week of June 13-19:''' | ||
+ | |||
+ | * ''Christian'' | ||
+ | ** EcoR1 digest of ligation product | ||
+ | ** Transformed Top 10 Cells with pBIB from ligation and plated | ||
+ | ** Inoculated 30 colonies | ||
+ | ** UNR mini prep on all 30 colonies | ||
+ | ** Digested Samples with HindIII and EcoR1 | ||
+ | ** QIAGEN mini prep on samples 11,12 &13 | ||
+ | ** Digested Samples with HindIII and EcoR1 | ||
* ''Bryson'' | * ''Bryson'' | ||
Line 162: | Line 227: | ||
** Single colony streaked four cell lines of ccdB gene in TOPO-clone: line 3, line 7, line 8, line 9 | ** Single colony streaked four cell lines of ccdB gene in TOPO-clone: line 3, line 7, line 8, line 9 | ||
** Ordered primers for Left Border Repeat of pBIB: pBIB-LB-F and pBIB-LB-R for sequencing of pBIB vector | ** Ordered primers for Left Border Repeat of pBIB: pBIB-LB-F and pBIB-LB-R for sequencing of pBIB vector | ||
+ | |||
+ | * ''Matthew'' | ||
+ | ** Miniprepped candidates and digested them | ||
+ | ** Ran on gel, some had strange bands, I want to retest | ||
+ | ** Colonies appear to not have eliminated EcoRI | ||
'''Week of June 20-26:''' | '''Week of June 20-26:''' | ||
+ | |||
+ | * ''Christian'' | ||
+ | ** Ran gel of Sample 11 | ||
* ''Bryson'' | * ''Bryson'' | ||
Line 184: | Line 257: | ||
** Primer Design of RD29A | ** Primer Design of RD29A | ||
+ | * ''Matthew'' | ||
+ | ** Attempted to test more candidates from hexameric ligation, no candidates had eliminated EcoRI | ||
+ | ** Team reevaluated its standing, given a month of failed attempts to modify pBIB | ||
+ | ** We are each assigned new tasks. I will be put in charge of making EYFP and mCherry with plant Kozak | ||
+ | ** I design primers to extract parts from iGEM vectors with Kozak sequences | ||
+ | |||
+ | ==JULY== | ||
'''Week of June 27-July 3:''' | '''Week of June 27-July 3:''' | ||
Line 193: | Line 273: | ||
** Made chlorophenocol resistant agar plates | ** Made chlorophenocol resistant agar plates | ||
** Agarose gel analyzed PCR products | ** Agarose gel analyzed PCR products | ||
+ | |||
+ | * ''Matthew'' | ||
+ | ** Transformed colonies with iGEM parts, miniprepped. | ||
+ | ** Attempted PCR on EYFP, Failed. Reevaluated protocol. | ||
'''Week of July 4-10:''' | '''Week of July 4-10:''' | ||
Line 202: | Line 286: | ||
* ''Elaine'' | * ''Elaine'' | ||
- | ** | + | ** Transformed ccdB into NEB, OmniMax, and DEB cells |
** Made LB/KAN plates | ** Made LB/KAN plates | ||
- | ** Took picture of ccdB Sensitivity Experiment 1 | + | ** Took picture of ccdB Sensitivity Experiment 1 Results |
** GFP Primer Design | ** GFP Primer Design | ||
Line 211: | Line 295: | ||
* ''Elaine'' | * ''Elaine'' | ||
** Made LB/Amp plates | ** Made LB/Amp plates | ||
+ | |||
+ | * ''Randy and Vadim'' | ||
+ | ** TOPOcloned pBIB fragment | ||
+ | ** Attempted to ligate ccdB into iGEM vector pSB1C3 | ||
+ | ** Single colony streaked ccdB transformation | ||
+ | ** Made Chloramphenicol broth | ||
+ | ** Performed PCR on pBIB cell lines | ||
+ | ** Digested ccdB in iGEM vector pSB1C3 with PstI and EcoRI | ||
+ | ** Miniprepped ccdB colonies | ||
+ | ** Gel analyzed pBIB PCR product | ||
+ | ** Transformed pSB1C3+RFP vector onto Chloramphenicol resistant plates | ||
+ | ** Made 50x TAE buffer | ||
+ | ** Miniprepped pSB1C3+RFP vector | ||
+ | |||
+ | * ''Matthew'' | ||
+ | ** Processed Miniprepped iGEM colonies for mCherry and EYFP | ||
+ | ** Set up PCR for mCherry, EYFP, and NOS | ||
'''Week of July 18-24:''' | '''Week of July 18-24:''' | ||
Line 217: | Line 318: | ||
** PCR of GFP | ** PCR of GFP | ||
** Ran agarose gel analysis of GFP PCR product | ** Ran agarose gel analysis of GFP PCR product | ||
+ | |||
+ | * ''Randy and Vadim'' | ||
+ | ** Amplified pBIB fragment using PCR | ||
+ | ** Gel analyzed pBIB PCR product | ||
+ | ** Attempted ligation of ccdB into iGEM vector pSB1C3 | ||
+ | ** Transformed ligation into NEB cells | ||
+ | ** Selected supposed colonies with ccdB+pSB1C3 | ||
+ | |||
+ | * ''Matthew'' | ||
+ | ** Analyzed PCR fragments on gels for mCherry, EYFP, and NOS | ||
+ | [[Image: Polasko_eyfpcherry_pcrreal.jpg|300px|thumb|left]] | ||
+ | <p> </p> | ||
+ | <p> </p> | ||
+ | <p> </p> | ||
+ | PCR results: worked for eyfp and mcherry with bands around 700bp. | ||
+ | <p>From Left: Lane 1 - Lamda Hind III Mlc. Marker.</p> | ||
+ | <p>Lane 2 - Uncut iGem vector</p> | ||
+ | <p>Lane 3 - EYFP</p> | ||
+ | <p>Lane 4 - EYFP</p> | ||
+ | <p>Lane 5 - EYFP</p> | ||
+ | <p>Lane 6 - mCherry</p> | ||
+ | <p>Lane 7 - mCherry</p> | ||
+ | <p>Lane 8 - mCherry</p> | ||
+ | <p>Lane 9 - 100bp ladder</p><p> </p> | ||
+ | <p> </p> | ||
+ | <p> </p> | ||
+ | <p> </p> | ||
+ | ** NOS PCR did not appear to work. | ||
+ | ** Performed transformation protocol with TOPO vector | ||
+ | ** Performed screening on Kan and miniprepped | ||
'''Week of July 25-31:''' | '''Week of July 25-31:''' | ||
+ | * ''Christian'' | ||
+ | ** Transformed Top 10 cells with pBIB and pMA (containing rd29A) | ||
+ | |||
+ | * ''Elaine'' | ||
+ | ** GFP Transformation | ||
+ | ** Cell Culture of GFP | ||
+ | ** Miniprep of GFP | ||
+ | ** EcoR 1 & Pst 1 Digest of GFP | ||
+ | ** Ran 1.2% agarose gel analysis of the GFP digest | ||
+ | <p>[[Image:GFP from iGEM (E0040) paint.jpg|500px]]</p> | ||
+ | * The "GFP E0040" gel analysis was successful for the expected bands of GFP showed at ~720 bp when digested with EcoR 1 & Pst 1 (labeled Cut #1, Cut #2, Cut#3, Cut#4). | ||
+ | ** PCR of GFP | ||
+ | |||
+ | * ''Randy and Vadim'' | ||
+ | ** Miniprepped ccdB+pSB1C3 colonies | ||
+ | ** Digested minipreps with EcoRI and PstI | ||
+ | ** Performed colony PCR on pSB1C3 colonies | ||
+ | |||
+ | * ''Matthew'' | ||
+ | ** Ran Digests and gels for candidates of mCherry, EYFP, and NOS in TOPO | ||
+ | ** 1 possible candidate each for mChery, EYFP, and NOS. | ||
+ | *** Nos bands did not show but sent one for sequencing anyway | ||
+ | |||
+ | ==AUGUST== | ||
'''Week of August 1-7:''' | '''Week of August 1-7:''' | ||
+ | |||
+ | * ''Christian'' | ||
+ | ** Designed and ordered primers for wt Arabidopsis isolation of DREB1C promoter region | ||
+ | ** Mini prep on pBIB and pMA inoculations | ||
+ | |||
+ | * ''Elaine'' | ||
+ | ** Ran 1.2% Agarose Gel analysis of GFP PCR product | ||
+ | <p>[[Image:GFP PCR product.jpg|500px]]</p> | ||
+ | * The "GFP PCR" gel analysis was successful for the expected bands of GFP + Primers showed at ~ 804bp for all PCR products (labeled 1 ng, 5ng, 10ng, & ~826ng) | ||
+ | ** Topocloned GFP PCR product | ||
+ | ** Cell Culture of GFP Topocloned colonies | ||
+ | ** Streaked colony plate | ||
+ | ** Miniprep of GFP Topocloned colonies | ||
+ | ** EcoR I digestion of GFP Topocloned | ||
+ | ** Ligation Test: GFP original vector digested with EcoR I | ||
+ | |||
+ | * ''Samantha and Christian'' | ||
+ | ** pMA and pBIB liquid cultures and mini preps | ||
+ | |||
+ | * ''Bryson'' | ||
+ | ** Designed and ordered primers for the 35S promoter | ||
+ | ** Made spectymycin plates | ||
+ | ** Transformed DB3.1 cells with pK7FWG2 | ||
+ | ** Liquid cultures and minipreps to isolate pK7FWG2 | ||
+ | |||
+ | * ''Randy and Vadim'' | ||
+ | ** Grew ccdB 8-2 on Kan. resistant plates | ||
+ | ** Gel analyzed colony PCR product from July 29 | ||
+ | ** Made additional LB broth | ||
+ | ** Gel analyzed ccdB+pSB1C3 ligation using EcoRI and Pst | ||
+ | *** Ligation was unsuccessful | ||
+ | ** Performed PCR cleanup on ccdB | ||
'''Week of August 8-14:''' | '''Week of August 8-14:''' | ||
+ | |||
+ | * ''Elaine'' | ||
+ | ** Ran 1.2% Agarose Gel analysis of GFP Topocloned EcoR I digest | ||
+ | <p>[[Image:GFP in Topo Vector 001.jpg|500px]]</p> | ||
+ | * The "GFP in Topo Vector" gel analysis was successful for the EcoR1 digested (cut samples labeled C1, C2, C3, C4, C5, & C6) samples shows bands at ~804bp (GFP + primers) and the Topo bands at ~ 3,519bp. | ||
+ | ** Ligation Test: Ligated EcoR I digest GFP original vector | ||
+ | ** Ligation Test: Transformed Ligation and EcoR I digest of GFP into NEB cells | ||
+ | ** Cell culture and streaked colonies of RFP in PSB1C3 vector | ||
+ | ** Miniprepped RFP in PSB1C3 vector | ||
+ | ** Digested both RFP in PSB1C3 vector & GFP Topo Vector together with EcoRI and PstI | ||
+ | ** Ethanol Precipitation of Digested RFP & GFP in PSB1C3 & Topo Vectors | ||
+ | ** Ligated the RFP & GFP in either PSB1C3 & Topo Vectors | ||
+ | ** Transformed RFP & GFP in either PSB1C3 & Topo Vectors by growing in NEB Cells in KAN & Chloramphenicol plates | ||
+ | |||
+ | * ''Samantha and Christian'' | ||
+ | ** Triple digest of pMA and pBIB with Hind III, Mfe I, and Eco RI | ||
+ | ** Ligation of triple digest products | ||
+ | |||
+ | * ''Bryson'' | ||
+ | ** PCR of pK7FWG2 | ||
+ | |||
+ | * ''Randy and Vadim'' | ||
+ | ** Made and aliquoted ligase buffer, ATP, and DTT for use for ligation | ||
+ | ** Ligated ccdB+pSB1C3, did not use EtOH precipitation | ||
+ | ** Miniprepped ccdB+pSB1C3 ligation | ||
+ | ** Digested and gel analyzed ligation using EcoRI and Pst | ||
+ | *** Ligation was unsuccessful | ||
+ | ** Ligated ccdB+pSB1C3 using EtOH precipitation | ||
'''Week of August 15-21:''' | '''Week of August 15-21:''' | ||
+ | |||
+ | * ''Elaine'' | ||
+ | ** Selected 20 colonies for cell culture and streaked into KAN & Chloramphenicol plates | ||
+ | ** Miniprepped 11 cell cultures that didn't grow in KAN plates which means it has to be GFP in PSB1C3 vectors | ||
+ | ** Digested GFP in PSB1C3 vectors with EcoR1 & PstI | ||
+ | ** Ran 1.2% Agarose Gels analysis of GFP in PSB1C3 vectors digested with EcoR1 & PstI | ||
+ | <p>[[Image:GFP in pSB1C3 iGEM Vector.jpg|500px]]</p> | ||
+ | * The "GFP in pSB1C3 iGEM Vector" gel analysis was successful for it showed at colony #17 (Digested/Cut sample labeled C17) the GFP (720) + primers [which includes the KpnI (GGT ACC = 6bp), Kozak sequence (AAA AAA AAA ACA = 12bp), & Translationsal Stop codon (TAATAA = 6bp)] band is at ~804bp and the pSB1C3 bands at ~2,072bp. | ||
+ | |||
+ | * ''Bryson'' | ||
+ | ** 1.2% gel to confirm presence of amplicon | ||
+ | ** Topocloning of amplicon and transformation of Topo vector into DB3.1 cells | ||
+ | |||
+ | *''Randy and Vadim'' | ||
+ | ** Miniprepped ligation from Aug. 13 | ||
+ | ** Digested and analyzed ccdB+pSB1C3 ligation using EcoRI and Pst | ||
+ | *** Ligation was unsuccessful | ||
+ | ** Ligated ccdB+pSB1C3 using EtOH precipitation | ||
+ | ** Made Chlor. resistant plates | ||
+ | ** Autoclaved labware | ||
'''Week of August 22-28:''' | '''Week of August 22-28:''' | ||
+ | |||
+ | * ''Christian'' | ||
+ | ** Ran PCR on genomic <i>Arabidopsis thaliana</i> DNA using custom primers | ||
+ | ** Ran gel of PCR product, no bands corresponding to DREB1C | ||
+ | |||
+ | * ''Elaine'' | ||
+ | ** Sequenced colony #11 & #17 of GFP in the PSB1C3 vectors (submitted 4: 11F, 11R, 17F, 17R) | ||
+ | ** Made chloramphenicol plates and cell cultures from colony #17 & streaked more of colony #17 | ||
+ | ** Miniprepped 8 cell cultures and nanodrop | ||
+ | ** Ran 1.2% Agarose Gel to check for DNA (GFP in PSB1C3 vector) | ||
+ | |||
+ | * ''Bryson'' | ||
+ | ** Isolated and streaked 6 colonies | ||
+ | ** Liquid cultures and minipreps of samples | ||
+ | ** Digest of samples with EcoRI and PstI to confirm presence of insert | ||
+ | |||
+ | * ''Randy and Vadim'' | ||
+ | ** Miniprepped colonies from ligation from Aug. 20 | ||
+ | ** Digested and gel-analyzed ccdB+pSB1C3 ligation | ||
+ | *** Ligation was unsuccessful | ||
+ | ** Ligated ccdB+pSB1C3 using EtOH precipitation | ||
+ | ** Made Chlor. resistant plates | ||
+ | |||
+ | * ''Richard and Nick'' | ||
+ | **Designed BioBrick-compatible primers to amplify CD2+-Promoter ''AtMRP3'' from ''A. thaliana'' genomic DNA | ||
+ | |||
+ | ==SEPTEMBER== | ||
+ | '''Week of August 29-September 4:''' | ||
+ | * ''Elaine'' | ||
+ | ** Ran 1.2% Agarose Gel to check for DNA (GFP in PSB1C3 vector) | ||
+ | ** Analysis of sequence of GFP (PSB1C3) | ||
+ | ** Sequencing analysis of colony #11 & #17 | ||
+ | |||
+ | * ''Bryson'' | ||
+ | ** Grew 20 mL liquid cultures of pSB1C3 and Topo vector to prepare for ligation | ||
+ | ** Miniprepped cultures and eluted in 300 microliters | ||
+ | ** 50 microliter digests done | ||
+ | *** 20 microliters were run on 1.0% agarose gel to confirm complete digestion of both plasmids | ||
+ | *** Digested plasmids were added in a roughly 1:1 ratio and ligated in a 40 microliter ligation reaction | ||
+ | |||
+ | * ''Randy and Vadim'' | ||
+ | ** Digested and gel-analyzed ccdB+pSB1C3 ligation from Aug. 27 | ||
+ | *** Ligation was unsuccessful | ||
+ | ** Performed PCR on ccdB | ||
+ | ** Ligated ccdB+pSB1C3 using Phenol:Chloroform cleanup techniques and EtOH precipitation | ||
+ | |||
+ | * ''Matthew'' | ||
+ | ** Sequence results from first attempt at mCherry,EYFP, and NOS failed. NOS abandoned. | ||
+ | ** Started over with new colonies, miniprepped, digested, ethanol precipitated, and ligated for Topo | ||
+ | ** Screened colonies on Kan and Amp, selected several to miniprep | ||
+ | ** Digested and ran on gels, identified several more candidates for sequencing for mCherry and EYFP | ||
+ | |||
+ | '''Week of September 5-11:''' | ||
+ | * ''Elaine'' | ||
+ | ** Sequenced 4 tubes of #17 of GFP in PSB1C3 | ||
+ | ** Digested rd29A with Hind III & MfeI-HF (for Chris' Project) | ||
+ | |||
+ | * ''Bryson'' | ||
+ | ** Transformation of ligation reaction | ||
+ | ** Plated on chloramphenicol | ||
+ | ** Selected four white colonies and single-colony streaked them | ||
+ | ** 4 mL liquid cultures of colonies | ||
+ | ** Miniprepped samples and eluted in 50 microliters | ||
+ | ** 20 microliter digests with EcoRI and PstI done to ensure insert was present in pSB1C3 | ||
+ | |||
+ | * ''Randy and Vadim'' | ||
+ | ** Transformed ccdB+pSB1C3 ligation from Sept. 3 into DB3 cells | ||
+ | *** Transformation unsuccessful | ||
+ | ** Made Chlor. resistant plates | ||
+ | ** Made new 3M NaOH stock | ||
+ | |||
+ | * ''Matthew'' | ||
+ | ** Miniprepped candidates for mCherry and EYFP in Topo vector | ||
+ | ** Ran digests and gels on topo candidates and submitted them for sequencing | ||
+ | ** Sequencing Results came back positive for mCherry and EYFP in Topo | ||
+ | *** mCherry showed a point mutation but it should not have an effect on translation | ||
+ | |||
+ | * ''Richard and Nick'' | ||
+ | ** Re-amplified CD2+ promoter from A. thaliana genomic DNA with ExTaq polymerase; several unspecific bands were seen on the gel; could be due to high sequence homology in AtMRP family | ||
+ | **Ran PCR product on a long gel and performed a gel extraction to isolate fragments that could be the CD2+ promoter | ||
+ | **Performed diagnostic digest of fragment extracted; fragment did not yield predicted digestion patterm; designed new primers | ||
+ | |||
+ | '''Week of September 12-18:''' | ||
+ | |||
+ | * ''Christian'' | ||
+ | ** PCR of DREB1C with custom primers using extaq instead of platinum taq using <i>Arabidopsis thaliana</i> columbian | ||
+ | ** Ran gel of PCR product | ||
+ | <p>[[Image: DREB1C_gel_1.jpg]]</p> | ||
+ | * Bands showed at ~500 bp for all samples | ||
+ | ** Sample 2 selected for Topo cloning | ||
+ | |||
+ | * ''Elaine'' | ||
+ | ** rd29A(pMA) with RFP(PSB1C3) EcoR1 & Pst I Digest | ||
+ | ** Ethanol Precipitation of digested synthetic RD29A + RFP(pMA) with RFP(PSB1C3) | ||
+ | ** Ligation of digested synthetic RD29A + RFP(pMA) with RFP(PSB1C3) | ||
+ | ** Transformation of ligated synthetic RD29A + RFP(pMA) with RFP(PSB1C3) | ||
+ | |||
+ | * ''Randy and Vadim'' | ||
+ | ** Miniprepped ccdB with Mfe site in TOPO vector | ||
+ | ** Miniprepped RFP in pSB1C3 | ||
+ | ** Digested and gel analyzed ccdB with Mfe samples using EcoRI and Pst | ||
+ | ** Digested ccdB in TOPO vector and RFP in pSB1C3 using EcoRI and Pst | ||
+ | ** Gel purified ccdB and pSB1C3 fragments from digested samples | ||
+ | |||
+ | * Samantha | ||
+ | ** Gel extraction of RD29A | ||
+ | |||
+ | * ''Matthew'' | ||
+ | ** Miniprepped, digested, and ran on gels candidates for mCherry and EYFP with Kozak | ||
+ | ** Several candidates possible for sequencing for EYFP and 3 candidates for mCherry | ||
+ | [[Image: Polasko_EYFPigem.jpg|300px|thumb|left]] | ||
+ | <p> </p> | ||
+ | <p> </p> | ||
+ | EYFP Results - although it's hard to gel w/o mlc. marker. The bands are the right size around 700bp and iGEM pSB1c3 backbone at 2kb | ||
+ | <p>From Left: Lane 1 - 100 bp ladder. Did not show</p> | ||
+ | <p>Lane 2 - Uncut EYFP candidate 1</p> | ||
+ | <p>Lane 3 - EYFP candidate 1</p> | ||
+ | <p>Lane 4 - Uncut EYFP candidate 2</p> | ||
+ | <p>Lane 5 - EYFP candidate 2</p> | ||
+ | <p>Lane 6 - Uncut EYFP candidate 3</p> | ||
+ | <p>Lane 7 - EYFP candidate 3</p> | ||
+ | <p>Lane 8 - Uncut EYFP candidate 4</p> | ||
+ | <p>Lane 9 - EYFP candidate 4</p> | ||
+ | <p> </p> | ||
+ | <p> </p> | ||
+ | <p> </p> | ||
+ | <p> </p> | ||
+ | [[Image: Polasko_mCherryigem.jpg|300px|thumb|left]] | ||
+ | <p> </p> | ||
+ | <p> </p> | ||
+ | <p> </p> | ||
+ | mCherry Results - although it's hard to gel w/o mlc. marker. The band in Lane 5 the right size around 700bp with the iGEM pSB1C3 backbone at 2kb | ||
+ | <p>From Left: Lane 1 - 100 bp ladder. Did not show</p> | ||
+ | <p>Lane 2 - Uncut mCherry candidate 1</p> | ||
+ | <p>Lane 3 - mCherry candidate 1</p> | ||
+ | <p>Lane 4 - Uncut mCherry candidate 2</p> | ||
+ | <p>Lane 5 - mCherry candidate 2</p> | ||
+ | <p>Lane 6 - Uncut mCherry candidate 3</p> | ||
+ | <p>Lane 7 - mCherry candidate 3</p> | ||
+ | <p>Lane 8 - Uncut mCherry candidate 4</p> | ||
+ | <p>Lane 9 - mCherry candidate 4</p> | ||
+ | <p> </p> | ||
+ | <p> </p> | ||
+ | <p> </p> | ||
+ | <p> </p> | ||
+ | |||
+ | '''Week of September 19-25:''' | ||
+ | * ''Elaine'' | ||
+ | ** 09/17/10 Submitted GFP with Kozak sequence (PSB1C3) into registry | ||
+ | ** 09/20/10 Mailed GFP with Kozak sequence (PSB1C3) to MIT. | ||
+ | ** Streaked single colonies [rd29A + RFP (PSB1C3)] and did Cell cultures | ||
+ | ** Miniprepped [rd29A + RFP (PSB1C3)]and digested with EcoR I and Pst I | ||
+ | ** Ran uncut and digested [RD29A + RFP (PSB1C3)] into 1.2 Agarose Gel | ||
+ | <p>[[Image:Rd29A promoter + RFP in pSB1C3 iGEM Vector.jpg|500px]]</p> | ||
+ | * The "rd29A promoter + RFP in pSB1C3 iGEM Vector" gel analysis was successful for it showed the rd29A + RFP bands at ~1,529 bp and the pSB1C3 bands at ~2,072bp. (Digested/Cut samples with EcoR1 and Pst 1 = labeled C1-2, C1-7, C1-9). | ||
+ | ** Submitted [rd29A + RFP (PSB1C3)] for sequencing | ||
+ | |||
+ | * ''Randy and Vadim'' | ||
+ | ** Concentrated gel purification sample from Sept. 16 | ||
+ | ** Ligated ccdB gene into pSB1C3 vector | ||
+ | ** Transformed ccdB+pSB1C3 ligation into DB3 cells | ||
+ | ** Miniprepped ccdB+pSB1C3 ligation | ||
+ | |||
+ | * Samantha | ||
+ | ** PCR RD29A from pMA plasmid | ||
+ | ** Confirm PCR reaction via agarose gel | ||
+ | |||
+ | * ''Matthew'' | ||
+ | ** Miniprepped and submitted candidates for sequencing for mCherry and EYFP with Kozak | ||
+ | ** Sequences came back positive for EYFP and mCherry | ||
+ | *** Point mutation in the mCherry but shouldn't affect the translation | ||
+ | |||
+ | ==OCTOBER== | ||
+ | '''Week of September 26-October 2:''' | ||
+ | |||
+ | * ''Christian'' | ||
+ | ** Topocloned DREB1C PCR product and spread on plates using Kan/Amp counter selection | ||
+ | ** 5 colonies selected and inoculated overnight at 37C | ||
+ | |||
+ | * ''Elaine'' | ||
+ | ** Miniprepped some more [RD29A + RFP (PSB1C3)] samples for submission | ||
+ | |||
+ | * ''Randy and Vadim'' | ||
+ | ** Digested and gel-analyzed ccdB-pSB1C3 ligation with EcoRI and Pst | ||
+ | *** Digest yielded successful ligation | ||
+ | https://static.igem.org/mediawiki/2010/b/bf/CcdB%2BpSB1C3_gel.png | ||
+ | ** Made Kan and Amp resistant plates | ||
+ | ** Made additional LB broth | ||
+ | ** Autoclaved labware and equipment | ||
+ | ** Miniprepped ligations from Sept. 23 | ||
+ | ** Submitted ligation for sequencing at the Nevada Genomics Center | ||
+ | ** Made glycerol stock of ligations from Sept. 23 | ||
+ | ** Transformed ligations from Sept. 23 into NEB cells | ||
+ | *** Plates yielded no growth-ccdB ligation successful | ||
+ | |||
+ | * Samantha | ||
+ | ** Gel purification of RD29A PCR product | ||
+ | |||
+ | * ''Matthew'' | ||
+ | ** Submitted Kozak-mCherry and Kozak-EYFP to iGEM | ||
+ | ** Cultured and miniprepped some of Elaine's GFP iGEM vector | ||
+ | ** Miniprepped, digested, ethanol precipitated, and began ligation on GFP iGEM with 35S in Topo | ||
+ | |||
+ | '''Week of October 3-9:''' | ||
+ | |||
+ | * ''Christian'' | ||
+ | ** Mini prep of 5 (DREB1C_1, DREB1C_2 etc) DREB1C Topo construct colonies | ||
+ | ** Digested results with EcoR1 and Pst1 | ||
+ | ** Ran products on 0.8% agarose gel | ||
+ | <p>[[Image: DREB1C_gel_2.jpg]]</p> | ||
+ | * Expected bands show at ~550 bp | ||
+ | ** Sent samples for sequencing analysis | ||
+ | ** Digested DREB1C_2 and RFP_pSB1C3 with EcoR1 and Pst1 | ||
+ | ** EtOH ppt of completed digest | ||
+ | ** T4 ligation (using custom buffer) | ||
+ | ** Digested Topocloned DREB1C_2 with EcoR1 and Spe1 | ||
+ | ** Digested YFP_pSB1C3 with EcoR1 and Xba1 | ||
+ | ** EtOH ppt of DREB1C/YFP digest products | ||
+ | ** T4 ligation (using custom buffer) | ||
+ | ** Transformed DREB1C/YFP ligation product into TOP 10 Cells and streaked using Kan/Chlor counterselection | ||
+ | |||
+ | * ''Elaine'' | ||
+ | ** Analyzed rd29A PCR product ran on an Agarose Gel by Samantha Lee. | ||
+ | <p>[[Image:Rd29A PCR product - Samantha Lee.jpg|500px]]</p> | ||
+ | * The "rd29A PCR product" gel analysis was successful for the rd29A PCR products of both #1 & #2 showed bands of the rd29A at ~836bp. | ||
+ | ** Topocloned Samantha Lee's PCR product #1 of rd29A | ||
+ | ** Streaked single colonies of rd29A (Topo Vector) | ||
+ | ** Cell cultured single colonies of rd29A (Topo Vector) | ||
+ | ** Minipreped rd29A (Topo Vector) and digested with EcoR 1 and Pst 1. | ||
+ | |||
+ | * ''Matthew'' | ||
+ | ** Completed ligation and began transformation for 35S-GFP candidates | ||
+ | ** Screened 35S-GFP candidates on chloramphenicol and kanamycin | ||
+ | ** Cultured,miniprepped,digested, and ran on gel 20 candidates | ||
+ | *** One candidate possible for sequencing | ||
+ | [[Image: Polasko_35sgfp.jpg|300px|thumb|left]] | ||
+ | <p> </p> | ||
+ | 35S-GFP Composite Results - With careful inspection of my gels, I believed Lane 3 was a good candidate. I was looking for 2 bands, the composite at about 1.8kb and the pSB1C3 backbone at 2kb. Although, the image is not clean, I believed I saw a second band emerging in between the molecular markers which were 2kb and 1.6kb, making that emerging band at 1.8kb. Sequencing would prove me right | ||
+ | <p>From Left: Lane 1 - 1 kb ladder.</p> | ||
+ | <p>Lane 2 - Uncut 35S-GFP candidate 1</p> | ||
+ | <p>Lane 3 - 35S-GFP candidate 1</p> | ||
+ | <p>Lane 4 - Uncut 35S-GFP candidate 2</p> | ||
+ | <p>Lane 5 - 35S-GFP candidate 2</p> | ||
+ | <p>Lane 6 - Uncut 35S-GFP candidate 3</p> | ||
+ | <p>Lane 7 - 35S-GFP candidate 3</p> | ||
+ | <p>Lane 8 - Uncut 35S-GFP candidate 4</p> | ||
+ | <p>Lane 9 - 35S-GFP candidate 4</p> | ||
+ | <p>Lane 10 - 35S-GFP candidate 5</p> | ||
+ | <p> </p> | ||
+ | <p> </p> | ||
+ | ** Submitted for sequencing 1 35S-GFP candidate | ||
+ | |||
+ | '''Week of October 10-16:''' | ||
+ | |||
+ | |||
+ | * ''Elaine'' | ||
+ | ** Ran rd29A (Topo Vector) gel. | ||
+ | <p>[[Image: Rd29A in TOPO Vector.jpg|500px]]</p> | ||
+ | * The "rd29A in Topo Vector" gel analysis was successful for it showed the rd29A bands at ~836 bp and the Topo bands at ~3,519 bp. (Digested/Cut samples with EcoR1 and Pst 1 = labeled C5, C6, C7, & C8). | ||
+ | ** Digested rd29A (Topo Vector) and RFP (pSB1C3)with EcoR1 and Pst 1. | ||
+ | ** Ethanol Precipitation of the rd29A (Topo Vector) and RFP (pSB1C3). | ||
+ | ** Ligation of the rd29A (Topo Vector) and RFP (pSB1C3). | ||
+ | ** Transformation of the rd29A (Topo Vector) and RFP (pSB1C3) to transform to what we want: rd29A (psB1C3 Vector). | ||
+ | |||
+ | |||
+ | * ''Christian'' | ||
+ | ** Transformed ligation product into Top 10 cells using Chloramphenicol and Kan selection | ||
+ | ** 5 colonies selected and inoculated overnight at 37C | ||
+ | ** Miniprep 5 cultures and digested with EcoR1 and Pst1 | ||
+ | ** Ran digests on 0.8% agarose gel | ||
+ | <p>[[Image: DREB1C_gel_3.jpg]]</p> | ||
+ | * Expected bands appeared at ~500 bp for sample 3 and sample 5 | ||
+ | ** Samples DREB1C_2.3 and DREB1C_2.5 selected and sent for sequencing | ||
+ | ** Sequencing data for DREB1C_2.3 had 0 mismatches and was selected | ||
+ | |||
+ | * ''Matthew'' | ||
+ | ** Sequencing results came back positive for 35S-GFP | ||
+ | ** Miniprepped 35S-GFP and made glycerol stock | ||
+ | |||
+ | * ''Richard and Nick'' | ||
+ | ** Amplified CD2+ promoter from A. thaliana genomic DNA with ExTaq polymerase; several unspecific bands were seen again on the gel; performed gel extraction on fragments of interest | ||
+ | |||
+ | |||
+ | |||
+ | |||
+ | '''Week of October 17-23:''' | ||
+ | |||
+ | * ''Elaine'' | ||
+ | ** 30 Cell cultures of rd29A (pSB1C3) | ||
+ | ** Minipreped 30 cell cultures expected to have the rd29A (pSB1C3). Concentrations were too low and therefore only 4 colonies were digested. | ||
+ | ** Digested 4 colonies (labeled as seen on the gel below: #1, #3, #13, #15) suspected to have the rd29A in the iGEM(pSB1C3) Vector | ||
+ | ** These 4 colonies were ran on a 1.2% Agarose gel for analysis - "rd29A in iGEM (pSB1C3) Vector" | ||
+ | <p>[[Image:Rd29A in pSB1C3 - Epic Failure.jpg|500px]]</p> | ||
+ | * The "rd29A in pSB1C3 iGEM Vector" gel analysis was NOT successful for the expected bands of the rd29A at ~836bp didn't show up on the digested (cut with EcoR1 & Pst 1) samples labeled C1, C3, C13, & C15. | ||
+ | * Due to the 30 single colonies that was unsuccessful in having the rd29A in pSB1C3 iGEM Vector, I proceeded to test 45 single colonies by using the colony PCR Technique and made sure I streaked the 45 single colonies on LB-Chloramphenicol plates. | ||
+ | ** Ran 45 Colony PCR samples expected to have the rd29A in the iGEM(pSB1C3) Vector on 1.2% Agarose gels | ||
+ | <p>[[Image:Colony PCR -21 - rd29A in pSB1C3 Vector.jpg|500px]]</p> | ||
+ | * The "Colony PCR # 21 of rd29A in pSB1C3 iGEM Vector" gel analysis was successful for 1 (colony PCR #21) out of 45 colonies showed an rd29A band at ~836bp.(Band is shown in the Lane labeled #21). | ||
+ | ** Minipreped 4 samples of the Colony PCR #21 (labeled 21-1, 21-2, 21-3, 21-4) and streaked them on LB-Chloramphenicol plate. | ||
+ | ** Saved glycerol stocks for 21-3 & 21-4 of the rd29A in pSB1C3 & placed in -80C freezer. | ||
+ | ** Sequenced Colony PCR #21 at the Nevada Genomics Center. | ||
+ | ** Minipreped 1 sample of the 1-9 rd29A + RFP in pSB1C3. | ||
+ | ** Saved 2 glycerol stocks for the 1-9 rd29A + RFP in pSB1C3. | ||
+ | |||
+ | * ''Christian'' | ||
+ | ** Sequencing of DREB1C_3 in pSB1C3 had 0 mismatches and was submitted as part BBaK414007 | ||
+ | ** 24 colonies selected from DREB1C/YFP transformation and run in colony PCR using custom DREB1C primers | ||
+ | ** Products of PCR reaction run on a 0.8% agarose gel | ||
+ | [[Image: DREB1C_gel_4.jpg]] | ||
+ | * Band at ~500 bp for colony 24 | ||
+ | ** Colony 24 was the only positive result | ||
+ | ** Colony 24 DREB1C/YFP construct was sent for sequencing | ||
+ | |||
+ | * ''Matthew'' | ||
+ | ** Submitted 35S-GFP to iGEM | ||
+ | |||
+ | * ''Richard and Nick'' | ||
+ | ** Performed diagnostic digests on fragments that could potentially be Cd2+ promoter; no fragments yielded positive digestion patter...back to the drawing board | ||
+ | |||
+ | |||
+ | '''Week of October 24-30:''' | ||
+ | |||
+ | |||
+ | * ''Elaine'' | ||
+ | ** Added rd29A (pSB1C3) into the registry | ||
+ | ** Submitted rd29A (pSB1C3) through the mail. | ||
+ | |||
+ | |||
+ | <p> </p> | ||
+ | <p> </p> | ||
+ | ---- | ||
+ | |||
+ | {| style="color:#FFFFFF;background-color:#FFFFFF;" cellpadding="3" cellspacing="1" border="1" bordercolor="#008000" width="100%" align="center" | ||
+ | !align="center"|[[Image:Nevada_CABNR.jpg|200px]] | ||
+ | !align="center"|[[Image:NV_INBRE_Logo.jpg|200px]] | ||
+ | !align="center"|[[Image:UNR_ASUN_logo.jpg]] | ||
+ | !align="center"|[[Image:Promega_logo.jpg]] | ||
+ | !align="center"|[[Image:Invitrogen_logo.jpeg]] | ||
+ | !align="center"|[[Image:Sda logo small.jpg]] | ||
+ | |} |
Latest revision as of 21:20, 27 October 2010
Team Nevada Notebook
Contents |
APRIL
Week of April 11-17:
- Christian
- Transformed pBIB into Top 10 Cells
- Bryson, Michael, Senny, Tyler
- Made tobacco cell (NT-1) media in Dr. Shintani's lab
Week of April 18-24:
- Bryson, Christian
- EcoRI digest of pBIB
- Made Na acetate buffer
- Christian
- Ran gel of EcoR1 Digested pBIB
MAY
Week of April 25-May 1:
- Bryson
- Ran agarose gel of EcoRI digest
- Matthew
- Team collaborated on pBIB assignment. Too many chefs in the kitchen.
- We decide to each tackle the pBIB problem in parallel
Week of May 2-8:
- Elaine
- Ran 0.8% agarose gel of EcoRI digest
- Made LB/KAN plates
- Spread for colonies
- Did miniprep for pBIB liquid cultures
- Matthew
- Miniprepped pBIB
- Ran EcoRI digest and Klenow
- Ethanol precipitated and ligated
Week of May 9-15:
- Christian
- EcoR1/Xba1 Digest of pBIB
- Did Mini prep on 4 cultures
- Bryson
- Ran 0.8% agarose gel of pBIB post-phenol:chloroform cleanup.
- Did minipreps on additional pBIB liquid cultures.
- Elaine
- Did XbaI and EcoRI digest of pBIB
- Ran 2 0.8% gels of each digest
- Did a miniprep and a Phenol:chloroform clean-up
- Ran 0.8% gel of the XbaI and EcoRI digest with the uncut pBIB
- Matthew
- Ligated and transformed
- Screened colonies, miniprepped, and digested, ran on gel
- No candidates had EcoRI eliminated
Week of May 16-22:
- Christian
- Generated glycerol stock of pBIB transformed Top 10 cells
- Inoculated 5 cultures of pBIB transformed Top 10 cells grown on Kan resistant plates
- Ran samples on gel after digest with EcoR1
- Bryson
- Klenow reactions of EcoRI digests
- Phenol:chloroform cleanup of pBIB prior to ligation
- Blunt-end ligation of klenowed pBIB
- Randy Pares and Vidim Gladwell
- Designed primers pBIB-RB-F, pBIB-RB-R, NOS 3'-Foward Nos3' reverse for sequencing the pBIB plant plasmid.
- Elaine
- Made LB/KAN plates
- Made 50mg/ml stock of KAN
- Made 1X TAE buffer
- Matthew
- Digested and tested more colonies, none worked
- Started over with pBIB and Klenow
- Ethanol precipitated and ligated
- Transformed
- Screened colonies, miniprepped, and digested, ran on gel
- No candidates had EcoRI eliminated
Week of May 23-29:
- Christian
- Miniprep on pBIB transformed Top 10 cells using "low copy #" modification
- Digested with EcoR1 and HindIII
- Bryson
- Incubated 50 mL liquid culture of E. coli with pBIB (samples 3).
- Miniprepped sample 3, using modified protocol for large/low-copy plasmids.
- EcoRI digest of uncut sample 3
- Prepared 5 mM dNTP stock
- Elaine
- Incubated 50 mL liquid culture of E. coli with pBIB (sample 4 & sample 5)
- Qiaprep miniprep of sample 4 & sample 5 according to manufacturer's modified protocol for large/low-copy plasmids
- Nanodrop of DNA recovery of miniprepped sample 4 & sample 5
- Randy and Vadim
- Sent pBIB vector to Nevada Genomics Center for sequencing with primers designed during the week of May 16-22
- Designed forward and reverse minimal ccdB primers for PCR and sequencing of ccdB gene
- Maxiprepped pBIB vector using QIAGEN QIAfilter Plasmid Maxi Kit
- Matthew
- Investigated alternative ways of eliminating EcoRI site.
- Want to try hexameric linkers
JUNE
Week of May 30-June 5:
- Christian
- Miniprep Top 10 Cells transformed with pBIB
- Bryson
- HinD3 digest of uncut sample 3
- Ran 0.8% gels of samples 1-5 to verify complete digestion by EcoRI
- Pooled uncut samples 3, 4 and 5 (pBIB-pool)
- Recieved 5 µg of pBIB from Randy and Vadim's maxi-prep (pBIB-maxi)
- EcoRI digest of pBIB-pool and pBIB-maxi
- Ran 0.8% agarose gel of EcoRI digests
- Klenow reactions of pBIB-pool and pBIB-maxi
- Made glycerol stocks of pBIB samples 1-5
- Elaine
- EcoRI digest of uncut pBIB sample 4 and 5
- HinD3 digest of uncut sample 4 & sample 5 as a positive control
- Ran 0.8% gels of samples 1-5 to see if EcoRI digest was successful
- Ethanol precipitation of the EcoRI digests of sample 4 & sample 5
- Nanodrop resulted to a low DNA content
- Worked with Bryson for the EcoRI digest of the 5µg of pBIB maxi-prep
- Ran 0.8% agarose gel of the pBIB maxi-prep EcoRI digest
- Modified all protocols of the Binary vector
- Randy and Vadim
- Calculated amount of reagent needed for Deep Vent DNA polymerase reaction (New England Biolabs)
- Programmed thermal cycler for PCR of ccdB gene
- Ran PCR for ccdB
- Prepared LB/KAN Broth
- Gel analyzed resultant ccdB PCR reaction with 1.2% agarose gel
- Reaction was unsuccessful
- Matthew
- Miniprepped pBIB
- Ran EcoRI digests
- Ran ethanol precipitation
- Ligated with several concentrations of hexameric linkers designed to destroy site
- Ran transformation, no colonies
- Believed procedures/conditions ran on ligation and transformation not ideal
Week of June 6-12:
- Christian
- Klenow reaction on EcoR1 digested pBIB
- T4 ligation on Klenow products
- Bryson
- Ligation reactions for pBIB-pool and pBIB-maxi
- Digested pBIB-pool and pBIB-maxi again with EcoRI to linearize any unmodified pBIB
- Transformed Top-10 Cells with modified pBIB (designated pBIB#)
- Obtained two colonies after overnight incubation
- Line-streaked the two colonies (pBIB# 1 and pBIB# 2) on an LB-Kan plate
- Randy and Vadim
- Uploaded pBI101, pBIN19, pBIB-KAN, and ccdB gene to Vector NTI
- Ordered second set of pBIB primers: pBIB-RB-F2, pBIB-RB-F3, pBIB-RB-R2, and pBIB-RB-R3 for sequencing of pBIB
- Modified thermal cycler conditions for PCR of ccdB gene
- Ran PCR for ccdB using HiFi DNA polymerase (Invitrogen)
- Gel analyzed resultant ccdB PCR reaction with 1.2% agarose gel and successfully amplified ccdB gene
- Maxiprepped pBIB vector using QIAGEN QIAfilter Plasmid Maxi Kit
- Matthew
- Miniprepped pBIB
- Ran Digestions and ethanol precipitation
- Ligated with hexameric linkers
- Transformed, had some colonies
Week of June 13-19:
- Christian
- EcoR1 digest of ligation product
- Transformed Top 10 Cells with pBIB from ligation and plated
- Inoculated 30 colonies
- UNR mini prep on all 30 colonies
- Digested Samples with HindIII and EcoR1
- QIAGEN mini prep on samples 11,12 &13
- Digested Samples with HindIII and EcoR1
- Bryson
- Prepared liquid cultures of pBIB# 1 and pBIB# 2
- Miniprepped liquid cultures of pBIB#
- EcoRI and HinDIII digests of pBIB#
- Ran agarose gel of pBIB cut and uncut, pBIB# uncut, pBIB# cut with EcoRI and pBIB# cut with HinDIII to confirm the absence of EcoRI site in pBIB#
- Single-colony streaked pBIB# 2 on a fresh LB-Kan plate
- Elaine
- Worked with Chris to incubate 30 liquid cell cultures
- Ran 0.8% gels of all 30 samples
- Randy and Vadim
- Topocloned ccdB gene into TOPO PCR Blunt II vector
- Determined concentration of pBIB maxipreps using PicoGreen analysis
- Single-colony isolated nine colonies of TOPO-cloned ccdB gene
- Miniprepped cultures of ccdB gene in TOPO-clone
- Digested minipreps using EcoRI
- Ran 1% gel for digested minipreps
- Single colony streaked four cell lines of ccdB gene in TOPO-clone: line 3, line 7, line 8, line 9
- Ordered primers for Left Border Repeat of pBIB: pBIB-LB-F and pBIB-LB-R for sequencing of pBIB vector
- Matthew
- Miniprepped candidates and digested them
- Ran on gel, some had strange bands, I want to retest
- Colonies appear to not have eliminated EcoRI
Week of June 20-26:
- Christian
- Ran gel of Sample 11
- Bryson
- Selected 3 colonies from pBIB# 2 (2-1, 2-2, 2-3) and streaked on a fresh LB-Kan plate
- Started 20 mL liquid cultures of 2-1, 2-2, and 2-3
- Miniprepped samples
- EcoRI and XbaI digests of samples to confirm that the EcoRI was gone and 2-1, 2-2, 2-3 arose from the same colony
- 0.8% agarose gel of digests
- Randy and Vadim
- Miniprepped isolated cultures of ccdB gene using QIAGEN QIAprep Spin Miniprep Kit
- Nanodropped minipreps
- Digested minipreps using EcoRI
- Ran 1% gel for digested minipreps
- Sent cell lines 7-2 and 8-2 for sequencing to Nevada Genomics Center with ccdB M13 Forward and Reverse primers added
- Analyzed ccdB samples using Vector NTI (Invitrogen)
- Sent cell lines 7-2, 8-2, and 9-1 for sequencing/resequencing to Nevada Genomics Center with ccdB M13 Forward and Reverse primers added
- Elaine
- Primer Design of RD29A
- Matthew
- Attempted to test more candidates from hexameric ligation, no candidates had eliminated EcoRI
- Team reevaluated its standing, given a month of failed attempts to modify pBIB
- We are each assigned new tasks. I will be put in charge of making EYFP and mCherry with plant Kozak
- I design primers to extract parts from iGEM vectors with Kozak sequences
JULY
Week of June 27-July 3:
- Randy and Vadim
- Prepared ccdB for MaxiPrep using QIAGEN QIAfilter Plasmid Maxi Kit
- Prepared thermal cycler protocol for pBIB vector
- Performed multiple PCR on pBIB vector
- Transformed ccdB into NEB cells unsuccessfully
- Made chlorophenocol resistant agar plates
- Agarose gel analyzed PCR products
- Matthew
- Transformed colonies with iGEM parts, miniprepped.
- Attempted PCR on EYFP, Failed. Reevaluated protocol.
Week of July 4-10:
- Randy and Vadim
- Agarose gel analyzed PCR products
- Transformed ccdB into NEB, OmniMax, and DEB cells
- Made Kanamycin resistant LB plates
- Elaine
- Transformed ccdB into NEB, OmniMax, and DEB cells
- Made LB/KAN plates
- Took picture of ccdB Sensitivity Experiment 1 Results
- GFP Primer Design
Week of July 11-17:
- Elaine
- Made LB/Amp plates
- Randy and Vadim
- TOPOcloned pBIB fragment
- Attempted to ligate ccdB into iGEM vector pSB1C3
- Single colony streaked ccdB transformation
- Made Chloramphenicol broth
- Performed PCR on pBIB cell lines
- Digested ccdB in iGEM vector pSB1C3 with PstI and EcoRI
- Miniprepped ccdB colonies
- Gel analyzed pBIB PCR product
- Transformed pSB1C3+RFP vector onto Chloramphenicol resistant plates
- Made 50x TAE buffer
- Miniprepped pSB1C3+RFP vector
- Matthew
- Processed Miniprepped iGEM colonies for mCherry and EYFP
- Set up PCR for mCherry, EYFP, and NOS
Week of July 18-24:
- Elaine
- PCR of GFP
- Ran agarose gel analysis of GFP PCR product
- Randy and Vadim
- Amplified pBIB fragment using PCR
- Gel analyzed pBIB PCR product
- Attempted ligation of ccdB into iGEM vector pSB1C3
- Transformed ligation into NEB cells
- Selected supposed colonies with ccdB+pSB1C3
- Matthew
- Analyzed PCR fragments on gels for mCherry, EYFP, and NOS
PCR results: worked for eyfp and mcherry with bands around 700bp.
From Left: Lane 1 - Lamda Hind III Mlc. Marker.
Lane 2 - Uncut iGem vector
Lane 3 - EYFP
Lane 4 - EYFP
Lane 5 - EYFP
Lane 6 - mCherry
Lane 7 - mCherry
Lane 8 - mCherry
Lane 9 - 100bp ladder
- NOS PCR did not appear to work.
- Performed transformation protocol with TOPO vector
- Performed screening on Kan and miniprepped
Week of July 25-31:
- Christian
- Transformed Top 10 cells with pBIB and pMA (containing rd29A)
- Elaine
- GFP Transformation
- Cell Culture of GFP
- Miniprep of GFP
- EcoR 1 & Pst 1 Digest of GFP
- Ran 1.2% agarose gel analysis of the GFP digest
- The "GFP E0040" gel analysis was successful for the expected bands of GFP showed at ~720 bp when digested with EcoR 1 & Pst 1 (labeled Cut #1, Cut #2, Cut#3, Cut#4).
- PCR of GFP
- Randy and Vadim
- Miniprepped ccdB+pSB1C3 colonies
- Digested minipreps with EcoRI and PstI
- Performed colony PCR on pSB1C3 colonies
- Matthew
- Ran Digests and gels for candidates of mCherry, EYFP, and NOS in TOPO
- 1 possible candidate each for mChery, EYFP, and NOS.
- Nos bands did not show but sent one for sequencing anyway
AUGUST
Week of August 1-7:
- Christian
- Designed and ordered primers for wt Arabidopsis isolation of DREB1C promoter region
- Mini prep on pBIB and pMA inoculations
- Elaine
- Ran 1.2% Agarose Gel analysis of GFP PCR product
- The "GFP PCR" gel analysis was successful for the expected bands of GFP + Primers showed at ~ 804bp for all PCR products (labeled 1 ng, 5ng, 10ng, & ~826ng)
- Topocloned GFP PCR product
- Cell Culture of GFP Topocloned colonies
- Streaked colony plate
- Miniprep of GFP Topocloned colonies
- EcoR I digestion of GFP Topocloned
- Ligation Test: GFP original vector digested with EcoR I
- Samantha and Christian
- pMA and pBIB liquid cultures and mini preps
- Bryson
- Designed and ordered primers for the 35S promoter
- Made spectymycin plates
- Transformed DB3.1 cells with pK7FWG2
- Liquid cultures and minipreps to isolate pK7FWG2
- Randy and Vadim
- Grew ccdB 8-2 on Kan. resistant plates
- Gel analyzed colony PCR product from July 29
- Made additional LB broth
- Gel analyzed ccdB+pSB1C3 ligation using EcoRI and Pst
- Ligation was unsuccessful
- Performed PCR cleanup on ccdB
Week of August 8-14:
- Elaine
- Ran 1.2% Agarose Gel analysis of GFP Topocloned EcoR I digest
- The "GFP in Topo Vector" gel analysis was successful for the EcoR1 digested (cut samples labeled C1, C2, C3, C4, C5, & C6) samples shows bands at ~804bp (GFP + primers) and the Topo bands at ~ 3,519bp.
- Ligation Test: Ligated EcoR I digest GFP original vector
- Ligation Test: Transformed Ligation and EcoR I digest of GFP into NEB cells
- Cell culture and streaked colonies of RFP in PSB1C3 vector
- Miniprepped RFP in PSB1C3 vector
- Digested both RFP in PSB1C3 vector & GFP Topo Vector together with EcoRI and PstI
- Ethanol Precipitation of Digested RFP & GFP in PSB1C3 & Topo Vectors
- Ligated the RFP & GFP in either PSB1C3 & Topo Vectors
- Transformed RFP & GFP in either PSB1C3 & Topo Vectors by growing in NEB Cells in KAN & Chloramphenicol plates
- Samantha and Christian
- Triple digest of pMA and pBIB with Hind III, Mfe I, and Eco RI
- Ligation of triple digest products
- Bryson
- PCR of pK7FWG2
- Randy and Vadim
- Made and aliquoted ligase buffer, ATP, and DTT for use for ligation
- Ligated ccdB+pSB1C3, did not use EtOH precipitation
- Miniprepped ccdB+pSB1C3 ligation
- Digested and gel analyzed ligation using EcoRI and Pst
- Ligation was unsuccessful
- Ligated ccdB+pSB1C3 using EtOH precipitation
Week of August 15-21:
- Elaine
- Selected 20 colonies for cell culture and streaked into KAN & Chloramphenicol plates
- Miniprepped 11 cell cultures that didn't grow in KAN plates which means it has to be GFP in PSB1C3 vectors
- Digested GFP in PSB1C3 vectors with EcoR1 & PstI
- Ran 1.2% Agarose Gels analysis of GFP in PSB1C3 vectors digested with EcoR1 & PstI
- The "GFP in pSB1C3 iGEM Vector" gel analysis was successful for it showed at colony #17 (Digested/Cut sample labeled C17) the GFP (720) + primers [which includes the KpnI (GGT ACC = 6bp), Kozak sequence (AAA AAA AAA ACA = 12bp), & Translationsal Stop codon (TAATAA = 6bp)] band is at ~804bp and the pSB1C3 bands at ~2,072bp.
- Bryson
- 1.2% gel to confirm presence of amplicon
- Topocloning of amplicon and transformation of Topo vector into DB3.1 cells
- Randy and Vadim
- Miniprepped ligation from Aug. 13
- Digested and analyzed ccdB+pSB1C3 ligation using EcoRI and Pst
- Ligation was unsuccessful
- Ligated ccdB+pSB1C3 using EtOH precipitation
- Made Chlor. resistant plates
- Autoclaved labware
Week of August 22-28:
- Christian
- Ran PCR on genomic Arabidopsis thaliana DNA using custom primers
- Ran gel of PCR product, no bands corresponding to DREB1C
- Elaine
- Sequenced colony #11 & #17 of GFP in the PSB1C3 vectors (submitted 4: 11F, 11R, 17F, 17R)
- Made chloramphenicol plates and cell cultures from colony #17 & streaked more of colony #17
- Miniprepped 8 cell cultures and nanodrop
- Ran 1.2% Agarose Gel to check for DNA (GFP in PSB1C3 vector)
- Bryson
- Isolated and streaked 6 colonies
- Liquid cultures and minipreps of samples
- Digest of samples with EcoRI and PstI to confirm presence of insert
- Randy and Vadim
- Miniprepped colonies from ligation from Aug. 20
- Digested and gel-analyzed ccdB+pSB1C3 ligation
- Ligation was unsuccessful
- Ligated ccdB+pSB1C3 using EtOH precipitation
- Made Chlor. resistant plates
- Richard and Nick
- Designed BioBrick-compatible primers to amplify CD2+-Promoter AtMRP3 from A. thaliana genomic DNA
SEPTEMBER
Week of August 29-September 4:
- Elaine
- Ran 1.2% Agarose Gel to check for DNA (GFP in PSB1C3 vector)
- Analysis of sequence of GFP (PSB1C3)
- Sequencing analysis of colony #11 & #17
- Bryson
- Grew 20 mL liquid cultures of pSB1C3 and Topo vector to prepare for ligation
- Miniprepped cultures and eluted in 300 microliters
- 50 microliter digests done
- 20 microliters were run on 1.0% agarose gel to confirm complete digestion of both plasmids
- Digested plasmids were added in a roughly 1:1 ratio and ligated in a 40 microliter ligation reaction
- Randy and Vadim
- Digested and gel-analyzed ccdB+pSB1C3 ligation from Aug. 27
- Ligation was unsuccessful
- Performed PCR on ccdB
- Ligated ccdB+pSB1C3 using Phenol:Chloroform cleanup techniques and EtOH precipitation
- Digested and gel-analyzed ccdB+pSB1C3 ligation from Aug. 27
- Matthew
- Sequence results from first attempt at mCherry,EYFP, and NOS failed. NOS abandoned.
- Started over with new colonies, miniprepped, digested, ethanol precipitated, and ligated for Topo
- Screened colonies on Kan and Amp, selected several to miniprep
- Digested and ran on gels, identified several more candidates for sequencing for mCherry and EYFP
Week of September 5-11:
- Elaine
- Sequenced 4 tubes of #17 of GFP in PSB1C3
- Digested rd29A with Hind III & MfeI-HF (for Chris' Project)
- Bryson
- Transformation of ligation reaction
- Plated on chloramphenicol
- Selected four white colonies and single-colony streaked them
- 4 mL liquid cultures of colonies
- Miniprepped samples and eluted in 50 microliters
- 20 microliter digests with EcoRI and PstI done to ensure insert was present in pSB1C3
- Randy and Vadim
- Transformed ccdB+pSB1C3 ligation from Sept. 3 into DB3 cells
- Transformation unsuccessful
- Made Chlor. resistant plates
- Made new 3M NaOH stock
- Transformed ccdB+pSB1C3 ligation from Sept. 3 into DB3 cells
- Matthew
- Miniprepped candidates for mCherry and EYFP in Topo vector
- Ran digests and gels on topo candidates and submitted them for sequencing
- Sequencing Results came back positive for mCherry and EYFP in Topo
- mCherry showed a point mutation but it should not have an effect on translation
- Richard and Nick
- Re-amplified CD2+ promoter from A. thaliana genomic DNA with ExTaq polymerase; several unspecific bands were seen on the gel; could be due to high sequence homology in AtMRP family
- Ran PCR product on a long gel and performed a gel extraction to isolate fragments that could be the CD2+ promoter
- Performed diagnostic digest of fragment extracted; fragment did not yield predicted digestion patterm; designed new primers
Week of September 12-18:
- Christian
- PCR of DREB1C with custom primers using extaq instead of platinum taq using Arabidopsis thaliana columbian
- Ran gel of PCR product
- Bands showed at ~500 bp for all samples
- Sample 2 selected for Topo cloning
- Elaine
- rd29A(pMA) with RFP(PSB1C3) EcoR1 & Pst I Digest
- Ethanol Precipitation of digested synthetic RD29A + RFP(pMA) with RFP(PSB1C3)
- Ligation of digested synthetic RD29A + RFP(pMA) with RFP(PSB1C3)
- Transformation of ligated synthetic RD29A + RFP(pMA) with RFP(PSB1C3)
- Randy and Vadim
- Miniprepped ccdB with Mfe site in TOPO vector
- Miniprepped RFP in pSB1C3
- Digested and gel analyzed ccdB with Mfe samples using EcoRI and Pst
- Digested ccdB in TOPO vector and RFP in pSB1C3 using EcoRI and Pst
- Gel purified ccdB and pSB1C3 fragments from digested samples
- Samantha
- Gel extraction of RD29A
- Matthew
- Miniprepped, digested, and ran on gels candidates for mCherry and EYFP with Kozak
- Several candidates possible for sequencing for EYFP and 3 candidates for mCherry
EYFP Results - although it's hard to gel w/o mlc. marker. The bands are the right size around 700bp and iGEM pSB1c3 backbone at 2kb
From Left: Lane 1 - 100 bp ladder. Did not show
Lane 2 - Uncut EYFP candidate 1
Lane 3 - EYFP candidate 1
Lane 4 - Uncut EYFP candidate 2
Lane 5 - EYFP candidate 2
Lane 6 - Uncut EYFP candidate 3
Lane 7 - EYFP candidate 3
Lane 8 - Uncut EYFP candidate 4
Lane 9 - EYFP candidate 4
mCherry Results - although it's hard to gel w/o mlc. marker. The band in Lane 5 the right size around 700bp with the iGEM pSB1C3 backbone at 2kb
From Left: Lane 1 - 100 bp ladder. Did not show
Lane 2 - Uncut mCherry candidate 1
Lane 3 - mCherry candidate 1
Lane 4 - Uncut mCherry candidate 2
Lane 5 - mCherry candidate 2
Lane 6 - Uncut mCherry candidate 3
Lane 7 - mCherry candidate 3
Lane 8 - Uncut mCherry candidate 4
Lane 9 - mCherry candidate 4
Week of September 19-25:
- Elaine
- 09/17/10 Submitted GFP with Kozak sequence (PSB1C3) into registry
- 09/20/10 Mailed GFP with Kozak sequence (PSB1C3) to MIT.
- Streaked single colonies [rd29A + RFP (PSB1C3)] and did Cell cultures
- Miniprepped [rd29A + RFP (PSB1C3)]and digested with EcoR I and Pst I
- Ran uncut and digested [RD29A + RFP (PSB1C3)] into 1.2 Agarose Gel
- The "rd29A promoter + RFP in pSB1C3 iGEM Vector" gel analysis was successful for it showed the rd29A + RFP bands at ~1,529 bp and the pSB1C3 bands at ~2,072bp. (Digested/Cut samples with EcoR1 and Pst 1 = labeled C1-2, C1-7, C1-9).
- Submitted [rd29A + RFP (PSB1C3)] for sequencing
- Randy and Vadim
- Concentrated gel purification sample from Sept. 16
- Ligated ccdB gene into pSB1C3 vector
- Transformed ccdB+pSB1C3 ligation into DB3 cells
- Miniprepped ccdB+pSB1C3 ligation
- Samantha
- PCR RD29A from pMA plasmid
- Confirm PCR reaction via agarose gel
- Matthew
- Miniprepped and submitted candidates for sequencing for mCherry and EYFP with Kozak
- Sequences came back positive for EYFP and mCherry
- Point mutation in the mCherry but shouldn't affect the translation
OCTOBER
Week of September 26-October 2:
- Christian
- Topocloned DREB1C PCR product and spread on plates using Kan/Amp counter selection
- 5 colonies selected and inoculated overnight at 37C
- Elaine
- Miniprepped some more [RD29A + RFP (PSB1C3)] samples for submission
- Randy and Vadim
- Digested and gel-analyzed ccdB-pSB1C3 ligation with EcoRI and Pst
- Digest yielded successful ligation
- Digested and gel-analyzed ccdB-pSB1C3 ligation with EcoRI and Pst
- Made Kan and Amp resistant plates
- Made additional LB broth
- Autoclaved labware and equipment
- Miniprepped ligations from Sept. 23
- Submitted ligation for sequencing at the Nevada Genomics Center
- Made glycerol stock of ligations from Sept. 23
- Transformed ligations from Sept. 23 into NEB cells
- Plates yielded no growth-ccdB ligation successful
- Samantha
- Gel purification of RD29A PCR product
- Matthew
- Submitted Kozak-mCherry and Kozak-EYFP to iGEM
- Cultured and miniprepped some of Elaine's GFP iGEM vector
- Miniprepped, digested, ethanol precipitated, and began ligation on GFP iGEM with 35S in Topo
Week of October 3-9:
- Christian
- Mini prep of 5 (DREB1C_1, DREB1C_2 etc) DREB1C Topo construct colonies
- Digested results with EcoR1 and Pst1
- Ran products on 0.8% agarose gel
- Expected bands show at ~550 bp
- Sent samples for sequencing analysis
- Digested DREB1C_2 and RFP_pSB1C3 with EcoR1 and Pst1
- EtOH ppt of completed digest
- T4 ligation (using custom buffer)
- Digested Topocloned DREB1C_2 with EcoR1 and Spe1
- Digested YFP_pSB1C3 with EcoR1 and Xba1
- EtOH ppt of DREB1C/YFP digest products
- T4 ligation (using custom buffer)
- Transformed DREB1C/YFP ligation product into TOP 10 Cells and streaked using Kan/Chlor counterselection
- Elaine
- Analyzed rd29A PCR product ran on an Agarose Gel by Samantha Lee.
- The "rd29A PCR product" gel analysis was successful for the rd29A PCR products of both #1 & #2 showed bands of the rd29A at ~836bp.
- Topocloned Samantha Lee's PCR product #1 of rd29A
- Streaked single colonies of rd29A (Topo Vector)
- Cell cultured single colonies of rd29A (Topo Vector)
- Minipreped rd29A (Topo Vector) and digested with EcoR 1 and Pst 1.
- Matthew
- Completed ligation and began transformation for 35S-GFP candidates
- Screened 35S-GFP candidates on chloramphenicol and kanamycin
- Cultured,miniprepped,digested, and ran on gel 20 candidates
- One candidate possible for sequencing
35S-GFP Composite Results - With careful inspection of my gels, I believed Lane 3 was a good candidate. I was looking for 2 bands, the composite at about 1.8kb and the pSB1C3 backbone at 2kb. Although, the image is not clean, I believed I saw a second band emerging in between the molecular markers which were 2kb and 1.6kb, making that emerging band at 1.8kb. Sequencing would prove me right
From Left: Lane 1 - 1 kb ladder.
Lane 2 - Uncut 35S-GFP candidate 1
Lane 3 - 35S-GFP candidate 1
Lane 4 - Uncut 35S-GFP candidate 2
Lane 5 - 35S-GFP candidate 2
Lane 6 - Uncut 35S-GFP candidate 3
Lane 7 - 35S-GFP candidate 3
Lane 8 - Uncut 35S-GFP candidate 4
Lane 9 - 35S-GFP candidate 4
Lane 10 - 35S-GFP candidate 5
- Submitted for sequencing 1 35S-GFP candidate
Week of October 10-16:
- Elaine
- Ran rd29A (Topo Vector) gel.
- The "rd29A in Topo Vector" gel analysis was successful for it showed the rd29A bands at ~836 bp and the Topo bands at ~3,519 bp. (Digested/Cut samples with EcoR1 and Pst 1 = labeled C5, C6, C7, & C8).
- Digested rd29A (Topo Vector) and RFP (pSB1C3)with EcoR1 and Pst 1.
- Ethanol Precipitation of the rd29A (Topo Vector) and RFP (pSB1C3).
- Ligation of the rd29A (Topo Vector) and RFP (pSB1C3).
- Transformation of the rd29A (Topo Vector) and RFP (pSB1C3) to transform to what we want: rd29A (psB1C3 Vector).
- Christian
- Transformed ligation product into Top 10 cells using Chloramphenicol and Kan selection
- 5 colonies selected and inoculated overnight at 37C
- Miniprep 5 cultures and digested with EcoR1 and Pst1
- Ran digests on 0.8% agarose gel
- Expected bands appeared at ~500 bp for sample 3 and sample 5
- Samples DREB1C_2.3 and DREB1C_2.5 selected and sent for sequencing
- Sequencing data for DREB1C_2.3 had 0 mismatches and was selected
- Matthew
- Sequencing results came back positive for 35S-GFP
- Miniprepped 35S-GFP and made glycerol stock
- Richard and Nick
- Amplified CD2+ promoter from A. thaliana genomic DNA with ExTaq polymerase; several unspecific bands were seen again on the gel; performed gel extraction on fragments of interest
Week of October 17-23:
- Elaine
- 30 Cell cultures of rd29A (pSB1C3)
- Minipreped 30 cell cultures expected to have the rd29A (pSB1C3). Concentrations were too low and therefore only 4 colonies were digested.
- Digested 4 colonies (labeled as seen on the gel below: #1, #3, #13, #15) suspected to have the rd29A in the iGEM(pSB1C3) Vector
- These 4 colonies were ran on a 1.2% Agarose gel for analysis - "rd29A in iGEM (pSB1C3) Vector"
- The "rd29A in pSB1C3 iGEM Vector" gel analysis was NOT successful for the expected bands of the rd29A at ~836bp didn't show up on the digested (cut with EcoR1 & Pst 1) samples labeled C1, C3, C13, & C15.
- Due to the 30 single colonies that was unsuccessful in having the rd29A in pSB1C3 iGEM Vector, I proceeded to test 45 single colonies by using the colony PCR Technique and made sure I streaked the 45 single colonies on LB-Chloramphenicol plates.
- Ran 45 Colony PCR samples expected to have the rd29A in the iGEM(pSB1C3) Vector on 1.2% Agarose gels
- The "Colony PCR # 21 of rd29A in pSB1C3 iGEM Vector" gel analysis was successful for 1 (colony PCR #21) out of 45 colonies showed an rd29A band at ~836bp.(Band is shown in the Lane labeled #21).
- Minipreped 4 samples of the Colony PCR #21 (labeled 21-1, 21-2, 21-3, 21-4) and streaked them on LB-Chloramphenicol plate.
- Saved glycerol stocks for 21-3 & 21-4 of the rd29A in pSB1C3 & placed in -80C freezer.
- Sequenced Colony PCR #21 at the Nevada Genomics Center.
- Minipreped 1 sample of the 1-9 rd29A + RFP in pSB1C3.
- Saved 2 glycerol stocks for the 1-9 rd29A + RFP in pSB1C3.
- Christian
- Sequencing of DREB1C_3 in pSB1C3 had 0 mismatches and was submitted as part BBaK414007
- 24 colonies selected from DREB1C/YFP transformation and run in colony PCR using custom DREB1C primers
- Products of PCR reaction run on a 0.8% agarose gel
- Band at ~500 bp for colony 24
- Colony 24 was the only positive result
- Colony 24 DREB1C/YFP construct was sent for sequencing
- Matthew
- Submitted 35S-GFP to iGEM
- Richard and Nick
- Performed diagnostic digests on fragments that could potentially be Cd2+ promoter; no fragments yielded positive digestion patter...back to the drawing board
Week of October 24-30:
- Elaine
- Added rd29A (pSB1C3) into the registry
- Submitted rd29A (pSB1C3) through the mail.
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