October

4/10/2010

• digest of 8 fragments with BsaI-HF @ 37°C for 1hr
  • 6x2ul of F1-8
  • 3ul NEB4 10x
  • 3ul BSA 10x
  • 11ul H₂O
  • 1ul BsaI-HF
• purification with Nucleotide Removal Kit
• NanoDrop concentration check:

5/10/2010

• assembly started with Quick ligase kit
• ~200ng of fragment DNA per reaction
• ligation time ~10min

25/10/2010

• ViroByte PCR with Phusion High-Fidelity Hot Start

PCR was set up as follows:

10 ul Phusion HF Buffer 5x 1ul of dNTP 0.5 ul of 100 um primers 2 ul of AAV template 36 ul of water

................................................ 98 °C/45 s ................................................ (1x 98 °C/15 s 72 °C/30 s ................................................ (35x) 72 °C/10 min ................................................ 4 °C/ hold

fragments 5-8 of AAV2 and 1-8 of AAV6

26/10/2010

• Assembly of 1-4, 5-8 and 1-8 assemblies

Touchdown Phusion HiFi PCR was performed according to the following protocol: ................................................ 98 °C/30s ................................................ (1x 98 °C/15 s 72 °C/15 s (- 1.0 °C/cycle) 72 °C/1 min ................................................ (17x) 98 °C/15 s 55 °C/30 s 72 °C/1 min ................................................ (20x) 72 °C/10 min ................................................ (1x) 4 °C/ hold ................................................

27/09/2010

AAV 1 fragments 1-4; 5-8 and 1-8 (full capsid) assembly

• • Gel loading scheme:
  • M - GeneRuler 1kb DNA ladder
  • F 1-4 - fragments 1-4 assembly
  • F 5-8 - fragments 5-8 assembly
  • F 1-8 - fragments 1-8 assembly
  • C 1-4 - fragments 1-4 control
  • C 5-8 - fragments 5-8 control
  • C 1-8 - fragments 1-8 control