SBB11Ntbk-NikitPatel

Constructing Basic Parts

Nikit Patel 11:30, 15 February 2011 (EST)

• Create 100uM stock of oligos: P_sbp_inR and SS50r
  
• Followed Cloning by PCR Protocol:
  

- Used construction files below to setup PCR

- Did first part of SOEing for P_sbp basic part

- Thermocycler Program: 2K55

Construction of P_sbp BglBrick basic part sbb1124
PCR ss50f/P_sbp_inR on MG1655	(247 bp, gp = A)
PCR P_sbp_inF/ss50r on MG1655	(492 bp, gp = B)
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PCR ss50f/ss50r on A+B	                (710 bp, EcoRI/BamHI)
Sub into pBjh1601KC-Bca1144 		(EcoRI/BamHI, 3131+910, L)
Product is pBjh1601KC-sbb1124           {P_sbp}
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P_sbp_inR	Reverse removal of EcoRI site in P_sbp	
CAATAAATTGCAGAAGTCATGTAGGCCTG		
P_sbp_inF	Forward removal of EcoRI site in P_sbp	
CAGGCCTACATGACTTCTGCAATTTATTG		
ss50f	sbp
aaaccGAATTCatgAGATCTgcggtcgttgtgtaggtatccag
ss50r	sbp
tttggGGATCCcaacatcagcttcaataccgttg

Part sbb1104                            {P_fadL}
PCR ss29f/ss29r on MG1655 gen.          (611bp, EcoRI/BamHI)
Sub into pBjh1601KC-Bca1144#5           (EcoRI/BamHI, 3131+910, L)
Product is pBjh1601KC-sbb1104           {P_fadL}
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ss29fForward Cloning of P_fadL     aaaccGAATTCatgAGATCTgctttttcagtcagcgccgccag
ss29rReverse Cloning of P_fadL     tttggGGATCCgataagtgccactgcgactgcgagagc

Nikit Patel 12:35, 17 February 2011 (EST)

• P_sbp Products A and B

- Ran preparative gel

- Lanes 2 and 3 from gel confirmed sizes around 250 and 500 bp respectively

- Bands were cut

- Performed Zymo Gel Purification on both A + B

- Setup and run PCR for SOEing using Zymo Gel Purified DNA as template. (Used 2K55 mode for thermocycler)

• P_fadL Products

- Ran analytical gel (prepped 2uL DNA + 5uL Dye)

- Band in lane 2 from gel confirmed size around 600 bp

- Perform Regular Zymo Cleanup

Nikit Patel 18:17, 18 February 2011 (EST)

• P_sbp SOEing PCR products

- Ran analytical gel

- Lane 2 from gel confirmed size around 750 bp. (SOEing worked!)

- Performed Regular Zymo Cleanup