User:Perry/Summer 2007

6/25/07

Received hisGFP_F_BB and GFP_R_BB primers, reconstituted at 100uM and diluted to 10uM, prepared PCRs with 45ul Supermix, 2ul hisGFP_F_BB (10uM), 2ul GFP_R_BB (10uM), 1ul pEGFP (1:1000 of 500ng/ul). Incubated 95dC 10min, (95dC 30s, 55dC 30s, 72dC 60s)x30, 72dC 10min, 4dC hold.

Previously performed 25ul digests using 21.25ul miniprep, 0.25ul BSA(100x), 0.5ul enzyme 1, 0.5ul enzyme 2, 2.5ul Buffer 2. Incubated 37dC 12h, 80dC 20min, 4dC hold.

• R0052 XbaI/PstI
• J04500 SpeI/PstI
• J04450 XbaI/PstI
• R0011-J06702 XbaI/PstI
• PDZ1 in Topo, XbaI/PstI
• PDZ2 in Topo, XbaI/PstI
• PDZ1+2 in Topo XbaI/PstI

Tried Clonewell. Gave up.

No bands for GFPmek PCR. Prepared 2 more PCRs with 10 cycles annealing at 45dC, and 20 cycles annealing at 55dC.

Reconstituted <bbpart>BBa_I3263</bbpart>, <bbpart>BBa_I3273</bbpart>, <bbpart>BBa_F1610</bbpart> in 15ul water, and transformed 1ul in 20ul Top10 cells. We will try to use these in a quorum sensing project.

6/26/07

Previously induced JLO66, -PDZ1, 2, 1+2, JLO159, -PDZ1, 2, 1+2...overnight, 1:40 dilution, 3h growth, add 1mM IPTG, 2h growth. Took out 100ul, spin down, resuspend in 100ul PBS.

Ran SDS-PAGE gel, 4ul of resuspended cells, 16ul water, 5ul sample buffer (5X). 150V for about 90min. Transferred to nitrocellulose with semi-dry blotting (20V for 30min). Stained with Ponceau, and saw very, very light bands. Left in blocking buffer overnight, rocker, 4dC.

Lane 1: SeeBlue2 ladder

Lanes 2-5: JLO66, -PDZ1, PDZ2, PDZ1+2 induced

Lanes 6-9: JLO159, -PDZ1, PDZ2, PDZ1+2 induced

Lanes 10-12: JLO159-PDZ1, PDZ2, PDZ1+2 not induced

Previously prepared 4.5ml liquid cultures of R0052, J04500, J04450, R0011-J06702, PDZ1, PDZ2, PDZ1+2. Did minipreps.

Prepared 25ul digests with 20.25ul DNA, 2.5ul Buffer 2, 1ul Enzyme 1, 1ul Enzyme 2, 0.25ul BSA.

• R0052 SpeI/PstI
• R0052 XbaI/PstI
• J04500 SpeI/PstI
• J04450 XbaI/PstI
• R0011-J06702 XbaI/PstI
• PDZ1 in Topo, XbaI/PstI
• PDZ2 in Topo, XbaI/PstI
• PDZ1+2 in Topo XbaI/PstI

Added 3ul Antarctic Phosphatase Buffer and 2ul Antarctic Phosphatase to R0052 SpeI/PstI, R0052 XbaI/PstI, J04500 SpeI/PstI.

Ran 1% 100ml agarose gel, 130V for 45min.

Lane 1: 1kb+

Lane 2-3: GFPmek PCR

Lane 4-6: PDZ1, 2, 1+2 XbaI/PstI

Lane 7: J04450 XbaI/PstI

Lane 8: R0011-J06702 XbaI/PstI

Lane 9: R0052 XbaI/PstI

Lane 10: R0052 SpeI/PstI

Lane 11: J04500 SpeI/PstI

Smears probably result from huge amounts of DNA in the digest. Cut out ~300bp insert bands from PDZ1 and PDZ2, 600bp insert band from PDZ1+2, ~1kb insert bands from J04450 and R0011-J06702, large vector bands from R0052 SpeI/PstI and XbaI/PstI, J04500 SpeI/PstI.

I NEED TO MAKE THIS GFPmek PCR WORK!!!

6/27/07

Incubated membrane with 5ml TBST (TBS + 0.1% Tween) + 5ml blocking buffer + 20ul anti-PDZ serum (1:500), 2h on shaker at room temp. Then washed 3x15min with TBST. Then incubated membrane with anti-mouse, anti-rabbit mix (1:15000) from Alain, 45min on shaker at room temp. Washed 2x10min TBST, 2x10min TBS, rinse with distilled water. Result? Crap. I didn't see any strong bands, maybe two very weak bands if I look hard enough.

Performed High Speed midiprep of BioBricks I13263, I13273, F1610. Sent off for sequencing with VF2 and VR primers.

A couple of days ago, I did a ligation of R0011-J06702 and J04450 (XbaI/PstI) into pSB2K3 vector (R0052 XbaI/PstI). I got a bunch of colonies that were red. Today, I did 5 streak/colony PCRs of each.