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Team:UC-Merced/Notebook
From 2012.igem.org
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2) 1KD FO1 FO2 FO3 100kb AD1 AD2 AD 1kD | 2) 1KD FO1 FO2 FO3 100kb AD1 AD2 AD 1kD | ||
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[[File:pcrmx1.png]] | [[File:pcrmx1.png]] | ||
[[File:pcrmx2.png]] | [[File:pcrmx2.png]] | ||
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Nanodrop results | Nanodrop results | ||
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[[File:1001ND.png]] | [[File:1001ND.png]] | ||
-DNA Digestion of AD and FO | -DNA Digestion of AD and FO | ||
Combine in two tubes: | Combine in two tubes: | ||
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[[File:rd1001.png]] | [[File:rd1001.png]] | ||
Revision as of 02:35, 4 October 2012
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September 19, 2012:DNA Extraction |
Data: 215 Cells/5 Squares = 43 cells/square x = 43*100*4*10^(-3) x = 43 cells/square (43/.004 mm^3) 1000100 = 1.075*10^9 cells/mL (2.5*10^(7)) cells / (1.075*10^9 cells) = .023mL of bacteria Then start the extraction using the mini-prep kit (insert link to mini prep kit protocol ) Turn on the thermomixer when the buffers are being added -Temp at 56 degree C for 10 minutes -Takes around 5 minutes to heat up Use filter tips since we’re working with DNA As a funny mess up, we ended up throwing away the glass slip for the hemocytometer!!! |
September 26, 2012:Glycerol stocks + Agar+ Nanodrop |
Nanodrop -add small drop of DiH2O 3 times -dab with kim wipe do not wipe -dab both top and bottom bend -log onto ND1000 program and select nucleic acid -add DIH2O with micropipette and close top 2x - add 1 micro liter of DNA to nanodrop, close and measure -save and print Results: 24.1 nanogram/microliter 260/280 = 1.82 260/230 = .49 Remember to clean machine with DI H2O after use! 1 M CaCl2 Protocol -calculate morality of 1M CaCl2 Mass = M*Vol*MW Mass = 14.702 grams per 100 mL of H2O Add 60 L H2O to beaker Add 14.702g CaCl2 to beaker and stir Add back to column and fill up to 100mL Use 150 mL filter until PIPES protocol Weight out 2.307 g of pipes solid Required solution must be at 7pH so add NaOH and measure pH using pH stripes or indicator Once at 7 pH add dH2O until 100mL Use 150 mL filter unit |
September 27, 2012:Antibiotic plates |
Calculations (Note: Dilution formula was used) Chloramphenicol: (6mg/mL)x=(.025mg/mL)(250mL) x = 1mL Kanamycin: (25 mg/mL)x = (0.05 mg/mL)(250mL) x = .5mL Streptomycin: (20mg/mL)x = (0.02 mg/mL)(250mL) x = .25 mL Antibiotic Plates (Con’t): Data 1. Chloramphencial: Recommended = 25microgram/mL, stock = 6 mg/mL 2. Kanamycin: Recommended = 50 microgram/mL, stock = 25 mg/mL 3. Strephtomycin: Recommended = 20 microgram/mL, stock = 20 mg/mL Note: Color coded the plates: Chloramphenciol (Green) Kanamycin (Orange) Strep/Chloram (Green Black) Bacterial Incubation with Antibiotics E coli W – no antibiotics FMJ 39- strepromycin (25microgram/mL) JW 228- Kanamycin (25 microgram/mL) Bba_K27300- 1000x Amp To make 1000x Amp (25mg/mL)V = (25microgram/mL)(5mL) V = 5 microliter Incubate bacteria in 5mL of LB with antibiotics Glycerol stocks of bacteria Note: Remember to use Aseptic Technique! -Mix 700 micro liter log phase culture with 300 microliter 50 % glycerol -Vortex -Store into cryotube -place in -80 degree C for storage Nanodrop for HTCC 2181 -Same procedure as the one above Results: -260/280: 1.78 -260/230: .17 -2 ng/microliter 260/280: 1.98 260/230: .13 1.4 ng/microliter 260/280: 2.53 260/230: .13 2.9 ng/microliter TAE buffer 1 x for electrophoresis Calculations C1V1 = C2V2 50V1 = (1x)(1000mL) V1 = 20mL of 50x Primer Stocks [100 micromolar primered stocks] -AD BB Pfx Add 633 microliter DH20 -AD GSA Bt Add 1213 micro lite rDH2O -FO GSA Tp Add 1314 microliter DH2O FO BB Sfx Add 615 microliter DH2O Diluted to 10 micromolar working volumes Incubated FMJ39 and JW 1228 for competent because not sure which strain will be used |
September 28, 2012:PCR & Solution prep |
CaCl 2 solution
Need 176 mL = 180 mL so V2 = 180 mL V1 = C2V2/C1 =(60mM x 180mL)/(1000mM) = 10.8mL (1M) CaCl2 =(15%*180mL)/ (50%) = 54 mL glycerol 50% = (10mM x 180mL)/(100mM) = 18 mL/82.8mL PIPES (100mM) =97.2mL/180mL DH2O? Calculations were done with 200 mL a. 12 mL CaCl2 C1 = .03M Vtot = 200mL b. 60 mL glycerol C1 = .5M c. 20 mL PIPES C1 = .1M Must be filter sterilized afterwards! PCR protocol 1. PCR ratios for 2.5x a. H2O 47.6microliter b. MgCl2 1.9 microliter c. 10x buffer 6.3 microliter d. DNTP 1.3 microliter e. Forward Primer 1.3 microliter f. Reverse Primer 1.3 microliter g. DNA template 1 microliter h. Taq Pol .5 microliter 2. Three different MgCl2 concentrations a. 1.5 mM 47.6microliter H2O b. 2.0 mM 47.0 microliter H2O c. 2.5 mM 46.4 microliter H2O Gel Agarose -Refer to Roche FAQ LabDNA agarose 1) Measured 75 g of agar 2) Ad 50 mL 1xTAE Buffer 3) Pour plate into gel box and let it sit Gel Electrophoresis 1 Load 5 micro liter loading dye into each sample 2. Prepare/plan your well load out 1kB FOl FOl5 FO2 100BP FO25 FO3 FO35 1kb ladder 1kb ADl AD15 AD2 100bp AD25 AD3 AD35 1kD ladder -Prepare samples -Add buffer to gel and remove combs -lod wells with 10 micro liter of sample and 10 microliter ladder -Run at 60*8D Remove gel/stop running Take image 2) 1KD FO1 FO2 FO3 100kb AD1 AD2 AD 1kD
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September 29, 2012:PCR Gel Agarose Images |
PCR Gel Agarose Images GE Healthcare: GFx PCR DNA: Gel Band Purification -Able to get DNA out of gel FO: ADH Eluted with 30 microliter of nuclease free H2O Introduction of plasmid DNA into cells CaCl2 competency cells -we prepared competent cells today note: step 2 of inoculation to OD540 of 0.375 takes 3.5 hours (estimate) -placed in -70 degree Celsius freezer
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October 1, 2012:Gibson Ligation |
Transformation using CaCl2 Trial 2 11:40am Inoculated another 400mL of LB+Strephomyocin with 4 mL of FMJ39 Placed in shaker at 37 degrees Celsius with 250 RPM 1 @ 590nm wavelength (nanodrop)
@ 590nm Gibson Ligation: Performed Gibson Ligation using Protocol w/kit Amount of DNA used: ADH: 1.4microliter FO: 1.5 micro liter
Gibson fraction gel Ran Gel using results of Gibson ligation step -Excised marked band and extracted using gel extraction kit -namedropped extracted eluted DNA 14.3 ng/ul, 37.7, 61.1 <-- 3 trial Average 45ng/ul Setup PCR on Gibson Ligated Parts -leave overnight in PCR machine Standard Parts Assembly -Set PCR for AD and FO using standard part primers and protocol supplied by Marcos Garcia-Ojeda -Run and purify on gel Gel Order (1kb) 1st piece FO1 FO2 Ladder AD1 AD2 2nd piece FO1 FO2 AD1 AD2 -Collect DNA from gel Nanodrop results
-DNA Digestion of AD and FO Combine in two tubes:
FO: 20uL AD: 50uL Total DNA taken for restriction enzyme FO: (10uL)(34.3ng/uL) = 343 ng AD: (10uL)(20.16ng/ul) = 201.6 ng Ligation Step: 34.3ug/20.7uL = 10ng/x X = 207uL/34.3 FO = 0.603 uL 201.6ug/20.7uL = 17g/x AD = 1.745 uL a. RxN Volumes
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October 2, 2012:Transformation |
Gel for Gibson-Ligated AD-FO DNA Gel Well Order 1kB Ladder Gel G2 (gene) blank (control) Excised marked band and extracted using Gel Purification Kit This band should contain the AD FO gene w/Eco R1 and Pstl site Nanodrop results- 2.7 ng/uL -PCR for more Gibson Assembly product done by Israel G1 is DNA G2 is H2O Used 1 uL of DNA from 10/1 @45ng/uL Transformation -Briefly centrifuged the ligation tubes -place the tubes on ice -thaw the competent cells on ice -add about 50 uL of cells into 4 tubes -one for FO -one for AD -one for straight plasmid -one for negative control -Add 5 uL of ligation rxn into corresponding vial -Tap to mix -Incubate tubes on ice for 30 minutes -Incubate tubes @ 47 degrees for 30s -place tubes back on ice -Incubate the tubes @ 37 degree Celsius, 300 rpm for 1 hr -Spread 20-200uL on plates over night -The on remain cells can be stored @ 4 degree Celsius
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