Team:Duke/Notebook

PCR of Z4EV from pMN10

• new oligos SpeI-Z4EV5p and NcoI-spc-Z4EV3p (diluted to 100uM)
• 4 tubes with 0, 0.3, 0.6, 1 uL template
• iGEM 3-step protocol with 65C anneal, 20 sec extend
• Note: did not dilute template beforehand (do this in future)

Results (04/08/2014): Lanes 2 and 3 produced band at ~0.7-0.8 kb (agarose gel)

• Expected band size 715 bp
• Control (no template) showed no band, lane 4 produced faint band
• Lanes 3 and 4 showed strong band at ~5-6 kb (template expected 5.1 kb)

Next steps:

• Run on gel to confirm (4/8)
• digest PCR product and dCas9/Mxi1 with SpeI/NcoI to ligate (4/8)

Agarose Gel with Z4EV PCR products

• PCR from 04/07/2014 of Z4EV from pMN10
• Results (04/08/2014): Lanes 2 and 3 produced band at ~0.7-0.8 kb (agarose gel)
• Expected band size 715 bp
• Control (no template) showed no band, lane 4 produced faint band
• Lanes 3 and 4 showed strong band at ~5-6 kb (template expected 5.1 kb)

PCR cleanup of Z4EV PCR products

• PCR from 04/07/2014 of Z4EV from pMN10
• Used only lanes 2 and 3 (successful from gel)
• Concentration 32.4 ng/uL in 50 uL

Restriction Digest of Z4EV PCR product and TDH3-dCas9-Mxi1

• Both with SpeI-HF and NcoI-HF in Cutsmart
• PCR from 04/07/2014 of Z4EV from pMN10 -- 50 uL (entire product) in 65 uL reaction
• dCas9 plasmid construct from CC 190ng/uL -- 20 uL in 65 uL reaction

PCR cleanup of Z4EV PCR digest product

• 04/08 digest of 04/07 PCR
• Results: Final concentration negligible, no DNA

Next steps:

• Z4EV PCR again from pMN10
• Digest of PCR in SpeI/NcoI
• Gel extraction of digested TDH3-dCas9-MxiI

PCR of Z4EV from pMN10

• Repeat of PCR from 4/7/14
• Oligos SpeI-ZeEV5p and NcoI-Spc-Z4EV3p
• Diluted pMN10 template to 1 ng/uL before use
• 8 tubes: 0, 0.3, 0.5, 0.5, 0.7, 0.7, 1.0, 1.0 uL template in 50 uL reaction
• iGEM 3-step protocol with 65C anneal, 20 sec extend
• Results (see 4/11): expected bands present, but concentrations too low

Gel Extraction of backbone (-TDH3) from TDH3-dCas9-Mxi1 digest

• Digest performed 4/8 with SpeI/NcoI
• Expected band sizes: 10.5 kb (backbone, desired piece), 637 bp (TDH3, removed piece)
• Obtained consistent band sizes, used 400 mg gel in extraction <
• Gel picture:
• Results: obtained 20 uL product at 55 ng/uL (froze for later use)

Next steps:

• Run gel of PCR
• Clean up PCR

Agarose gel to analyze PCR of Z4EV from pMN10

• PCR from 4/10
• Expected band size: 715 bp
• Showed band at expected size in all seven non-control lanes
• Intensities appear low, increase in higher lanes (higher template conc.)
• Gel picture:

PCR cleanup of Z4EV from 4/10 PCR

• final concentration from 7 tubes: 25.8 ng/uL in 30 uL
• Need to improve

Next Steps:

• Redo PCR of Z4EV. Things to try:
• Use previous cleanup as a template
• use 1 uL enzyme instead of 0.5
• slightly longer extension time
• higher template concentration
• PCR cleanup: Things to try:
• Run PB buffer flow-through back through filter during step 7
• let PE buffer sit in column (covered) while ethanol evaporates
• let elution buffer sit on DNA for 2-3 minutes before spin